Welcome to my Guestbook!

Lynette Shingleton - 12/20/00 06:13:32
My Email:rshingle@callplus.co.nz

Comments:
I have a 2 year old neice that has just been diagnosed. It was a shock and we are still learning about it. She plays with my 2 year old twin girls every day.

Amy - 12/13/00 00:22:56
My Email:Metzger@aol.com

Comments:
Your page is the best one I have ever seen i have a 19 month old daughter with Cf your website is inspiring.

stacy - 12/10/00 20:19:31
My Email:sllovj@aol.com

Comments:
Iloved your page!I have a two year old daughter abbie who has cf we are in the process of getting the vest she hates chest pt.

Grandma Butler - 12/10/00 17:30:53
My Email:butler@bright.net

Comments:
I always knew you were such a cutie! Love you!!!

Tina M. Karhoff - 12/03/00 23:38:31
My Email:tmkgah@yahoo.com

Comments:
Hello!!! You did a wonderful job on the web page for Tanner! Tanner is in my prayers. God bless!

judykisseberth - 11/11/00 21:42:33
My Email:lbmrskizz@bright.net

Comments:
hi tanner, you don't know me but we are related. I just visited your web site at the suggestion of gloria dysert(my mom). you are such a handsome young man, and my prayer for you is that God will watch over you and that a cure will be found soon. you be good boy, santa will be here before you know it. God Bless you cousin judy

KENNY & GLORIA DYSERT - 11/10/00 03:30:50
My Email:tillie7425@aol.com

Comments:
Tanner is a very brave little boy and so cute.

Haze - 11/10/00 01:33:18

Comments:
Tanner you are a precious handsome child, i believe you can fight the disease that's in you. Just believe in yourself and don't ever give up. Remember your mom and dad will always be by your side to help you through the goods and bad. God will always guid you and help you on the way. Wish you the best!! Haze

jen - 11/08/00 04:57:36
My Email:mavretic@attcanada.ca

Comments:
what a beautiful page!!the words you have written seem like they have come out of my own mouth, for I have a daughter I feel the same way about.How touching and I'm glad I'm not the only parent going through these things,which now have become every day li e.Thank you. JEN

crystal oppelt - 11/02/00 22:00:55
My Email:nikechik4ever@aol.com

Comments:
hi. my name is crystal. i am 19 and i have cf. i had a double lung transplant in oct of 98. just wanted to say hi and i am here for ya. us cf patients have to stick together.

Amanda and Emily Stainbrook - 10/26/00 17:26:08

Comments:
Hey how are you all? Tanner you still being a goffy little boy? The web page is really cute we love it! Well talk to you all later. Love, Amanda and Emily

Lisa - 10/07/00 19:34:06
My Email:gaffney@email.chop.edu

Comments:
I am a nurse at The Children's Hospital of Phila. and was doing some research for graduate school. Unfortunately I haven't gotten very far as I have been distarcted by so many inspirational stories. God Bless you and your family, your enthusiasm is inspir ng.

Stephanie - 09/25/00 19:24:27
My Email:sjbsjbsjb@hotmail.com

Comments:
I just want to say god bless your family. Our son goes thursday to akron childrens hospital to see if he has sf. Were praying that he don't. My prayers our with you.

moira hall - 09/25/00 02:17:53

Comments:
you did a beautiful job

Renee Coffey - 09/11/00 08:19:23
My Email:samneric_rey@hotmail.com

Comments:
It is a touching page. I live in Australia and am 18 years old. I have lost two dear freinds in the last year to CF. The first was Rhelma. At her funeral, my friend Amy held my hand all the way through and made everything ok. Little did I know her fu eral would be next, 6 months later. CF kids have a spirit about them. YOur son definately has this spirit. God bless you.

Didi Diller (Allen) - 09/10/00 02:32:53
My Email:didi_allen@hotmail.com

Comments:
Stay strong Tanner!

Joanne - 09/05/00 18:02:07

Comments:
He is so cute. I am so sorry about your son. I know and feel your pain because I loss my friend with cf on my birthday, Apr,1999.

Michelle (Borer) Hermiller - 09/04/00 16:09:44
My Email:michelle@wcoil.com

Comments:
Dearest Tanner, You don't know me, but I am a friend of your mommy's. You're determination to beat this disease makes you a true inspiration to others. You are a beautiful little boy who I know will be a part of that miracle... the cure. Take good care of yourse f and know that so many people are thinking of you and praying for you!!! Sincerely, Michelle Hermiller

Shari Leonard - 08/30/00 02:44:57
My Email:sharileo@pionet.net

Comments:
I wanted to find out info on cystic fibrosis as I am the chairman of the committee at work to raise money for the United Way/Chad campaign. I wanted to get as much info as possible, in order to make people see the need to support the research needed to find a cure. God Bless Your Family.

Kathy Sabadosa - 07/28/00 20:49:09
My Email:kathryn.a.sabadosa@valley.net

Comments:
I visited your web site taking a break from my many hours of reading about CF. My son Jack was diagnosed with CF the second day after his birth and had surgery on his intestines. We just went to our first CF clinic yesterday. Best wishes to you and you family. Carpe Diem!

Patty - 07/11/00 01:28:32
My Email:PamH622@aol.com

Comments:
your page is so nice. i am the mother of 2 daughters with cf

Jaime - 07/04/00 19:54:05
My Email:boardhoarder@hotmail.com

Comments:
We have a 4yr old daughter that has CF. She has a milder form of the disease. Creating more lung problems than digestion problems. I truly feel blessed having her in our life. She goes to Rainbow babies and Childrens Hosp. in Cleveland Ohio. Thank you f r Sharing with us. Our prayers are with your family.

Alicia Smith - 07/03/00 20:34:58
My Email:aasmith@hotmail.com

Comments:
My son Zachary was diagnosed about a year ago with. CF sometimes I find all that he has to go through so difficult. I was looking for some positive feed back. Thanks Alicia

Cynthia Kirby - 07/02/00 03:13:46

Comments:
My Dear Tanner, I pray that both you and your parents will keep LOVE, HOPE, DETERMINATION and COURAGE strong within each of your hearts. I'm now 46 years old and the Lord still never ceases to amaze me, especially through the difficult times!

Cynthia Kirby - 07/02/00 03:02:35

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Pam DeMatteis - 06/27/00 00:33:46
My URL:http://forcomm.net
My Email:ademattis@forcomm.net

Comments:


AMY CARNES - 06/22/00 13:29:25
My Email:SAMANDAMY@BOERNENET.COM

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Stephanie - 06/14/00 07:39:04
My Email:eveangel1212

Comments:
Tanner: You and your parents are and inspiration for the rest of the world. I commend you on your courage and your parents for having the heart to deal with this fatel disease. I wish you the best in the years to come and your parents the best of luck in life, ove, and your family's pursuit of happiness.

Alissa Robitaille - 06/06/00 21:22:03
My Email:StArY1216

Comments:
very touching, even for me being 14, i care alot and i wish their was something i could do for those with the horrible disease

johanna & ray - 06/06/00 21:07:58

Comments:
we're just surfing the net and found your homepage we're bothin Texas Childrens Hospital for atuneup and just wanted tosay we like your pictures.

Chris Hipsher - 06/05/00 04:30:25
My URL:http://members.aol.com/reggieb123
My Email:Pray4Michael@aol.com

Comments:
Hey Tanner! Just checking in to see how you've been lately!! You're still in my prayers everyday. Hope you're doing well. God bless.

Karen Reed - 06/03/00 04:14:59
My Email:reed4life@tah-usa.net

Comments:
I have a 6 year old son with C.F. Ryan was diagnosed when he was a little over a year old. Your story was so real and familiar to us! It was very inspirational.

Avis Roiger - 05/30/00 17:50:09
My Email:aroiger@innotek-ep.org

Comments:
I have a new grandson, Joshua Anthony Roiger, born May 22, 2000. He weighed 9lbs. 5oz. and is 22 inches long. He is so beautiful! Joshua was diagnosed with CF the day of his birth. We now know God intended him to able to be a brave little boy so he ga e him his extra weight. You are such an inspiration, Tanner. I enjoyed your web page so very much. You are a beautiful young man and you have beautiful parents that love you with all their hearts. Love them forever, Tanner. We have a lot to learn abo t caregiving. We are fortunate Joshua is at Children's Hospital in Minneapolis. He will probably be there for another 2-3 weeks, depending on his feeding, etc. We are just beginning to learn what your parents already know. I'll talk with you again soon! In the meantime, God Loves You! Your Friend, Avis

sarah badeau - 05/27/00 04:51:30
My Email:brian.badeau@worldnet.att.net

Comments:
Great site. Keep up the fight. My husband and I are both carriers. One of our daughters is and one is not. I admire your courage.

- 05/26/00 19:37:03

Comments:
a beautiful son and a beautiful page! Good luck and God bless you

Julie - 05/21/00 19:45:47
My Email:Artemis295@aol.com

Comments:
Great page... I came here to find some more info on cf because I am going to be a nanny this summer for a 4 year old boy who has cf, and I want to learn more so I can meet his needs better. This page was great to see how others are dealing with cf.

Karen - 05/20/00 19:35:13
My Email:krnbrown@mindspring.com

Comments:
I like your home page....I am a grandmother with two grandbabies with CF.......Kaitlyn is 6 and Jerrod is 4...they also use the vest....they were in the hospital several stays their first year...Katie was born premature with a ruptured intestine...that i when we found out about her having CF....Jerrod we knew from the start...has they tested when he was still in his Mommy's tummy.....Katie has problems with weight...she is very dainty......I will tell my daughter about your site...

Lisa - 05/19/00 17:07:21
My Email:Browneyz46@aol.com

Comments:
hey, I think it's great how you're coping with all of this... I know it must be hard. I just recently found out that one of my best friends has cystic fibrosis... I was broken hearted. But after reading all of this, I feel a lot better. Thanks... I hope t ey find a cure for CF

Marcia Sherman - 05/17/00 22:39:23
My Email:Puccino@AOL.com

Comments:
Your web page is just beautiful. My 2 year old granddaughter was just diagnosed with CF. We are all still in a state of shock. We all want to learn more about it so we can help Danielle better cope with her illness. We would like her to be able to lead s normal a life as possilbe. Please tell me where I can get more information about the treatments and therapies available for CF. I would also like to find out about support groups so I can be in touch with other families who are dealing with this illnes . If anyone lives on Long Island, New York and would like to talk more about it, you can e-mail me at Puccino@AOL.com. Take care Tanner and keep up the good work.

Jennifer - 05/17/00 15:26:29
My Email:dsimp@leru.net

Comments:
We have a 7 year old daughter with (CF). She was just diagnosed about 3 months ago after all these years of misdiagnosis.She is doing alot better now but we would like to have the therapy vest for her because in my opinion it would do much more than the clapping we do now,but our insurance will not pay or it because they say it is not medically necessary,so if you have any information on how we may be able to get one I would appreciate it if you could let me know. We are doing the walk for (CF) on June 10th,but if you have information on anymore fundrai ers in the future we would appreciate it if you could let us know.Best of luck with your little boy!!!

Maribel Luteran - 05/17/00 12:00:43
My Email:mluteran@ocnjcc.org

Comments:
What a touching letter! My 5 mounth Lauren was just diagnosed last week. We are still in the initial shock stage. We hope to a part of miracle too. Good luck. Love, The Luterans

Michelle - 05/17/00 04:22:52
My Email:chases@jscomm.net

Comments:
Enjoyed your page. It was very encourging..My 7 year old grandaughter was diagnosed 2 months ago..after 4 bouts with pneumonia,several bout of bronchitis and more...She was misdaignosed for 7 years with asthma and allergies. She now has permanent lung da age on one side but with the right treatment is doing remarkably well...Better than she has in all 7 years prior..The doctor would like for her have a vest but insurance will not pay for one right now so we are looking for hep on the internet to see if we can locate one that someone might have for sale...It's good to know we are not alone in this fight.Keep up the good work.

Kanett W. - 05/16/00 20:40:17
My Email:Kanettwill@aol.com

Comments:
Hello, 5/16/00 My co-worker has a baby girl who was diagnosed with CF one week ago. I wanted to learn more about CF and decided to search the internet for answers. I came across your site and read Tanner's story. I just wanted to say that God still works miracles. Ju t trust and have faith that a miracle is being performed right now in Tanner's behalf. Tanner, May God shower you with grace, mercy and long blessed life. Peace!

Julie Bashaw - 05/10/00 21:53:58
My Email:jbashaw@unitedevv.com

Comments:
My nephew has CF. He is 5 years old and just diagnosed. Thanks, for your information and hugs, kisses and prayers to you

Julie Bashaw - 05/10/00 21:37:37
My Email:jbashaw@unitedevv.com

Comments:


Annette Laugher - 05/04/00 23:02:32
My Email:abe_wagner@hotmail.com.au

Comments:
Fantastic website! Keep well and strong little man! Lots of Love "From Australia" (The Wagner Family) Annette (Mum), Bill (Dad), Emily (18 months) and Samuel (8 months)

Kinga - 05/03/00 18:23:53
My Email:kinga.balogh@student.sh.se

Comments:
Hello! I came across this website when doing a research on CF. I will soon be a PH.d. student in molecular cell biology at Stockhols University, Sweden. The reason why I'm signing this Guestbook is to let you to know, that your webpage has inspired me a l t! I'm looking forward to come out of school and start research work because I want to help children like your son. I think you made something special with this website for your son, I will keep you in my prayers. Kinga from Sweden

Dana Bledsoe - 04/27/00 03:28:53
My URL:http://Jesicakes.homestead.com/jesicakes.html
My Email:bledsoe@citynet.net

Comments:
I too have a beautiful blonde with CF and we also go to Cincinnati Children's Hospital. Please feel free to e-mail me.

Ashley - 04/26/00 20:09:52
My Email:Panthergrl34@aol.com

Comments:
I read thru ur stuff because i am doing a research project. :o) you are a bright little boy! I wish you the best hun! Good Luck Ashley~ 16 yrs old

Kim Walters - 04/24/00 00:33:21
My Email:mybabieblues27@yahoo.com

Comments:
My 4 year old son has CF also and I accidentally stumbled onto your site. I love it, I laughed, I cried and it is a marvelous page. Your son is beautiful. Thank you. Devin's mom

matt - 04/20/00 02:47:03
My Email:edlydeen@prodigy.net

Comments:
my name is matthew. i have cf too. Im 6.5 years old.

matt - 04/20/00 02:44:35

Comments:


Chrystie and Arnaud - 04/19/00 21:34:07
My Email:chrystie@waika9.com

Comments:
Very nice and pleasant site. This is an E-mail from France. We are the parents of a 9 months old girl with CF.Her name is Ines. She was diagnosed 4 months ago. She is a very energetic and enthousiastic child. We also have a little daughter, Loren, who is exactly Tanner's age (she was born on february 22nd 1996). She is very helpful and understanding with her sister . She doesn't have CF. Such a site is very interesting,thanks for the info on vest. We need information, especially to compare treatments in France and in the US. Lots of love and courage to you Tanner.

Chrystie and Arnaud - 04/19/00 21:33:36
My Email:chrystie@waika9.com

Comments:
Very nice and pleasant site. This is an E-mail from France. We are the parents of a 9 months old girl with CF.Her name is Ines. She was diagnosed 4 months ago. She is a very energetic and enthousiastic child. We also have a little daughter who is exactly Tanner's age (she was born on february 22nd 1996). She is very helpful and understanding with her sister . She doesn't have CF. Such a site is very interesting,thanks for the info on vest. We need information, especially to compare treatments in France and in the US. Lots of love and courage to you Tanner.

- 04/19/00 21:30:38

Comments:


Chrystie and Arnaud - 04/19/00 21:28:42
My Email:chrystie@waika9.com

Comments:
Very nice and pleasant site. This is an E-mail from France. We are the parents of a 9 months old girl with CF.Her name is Ines. She was diagnosed 4 months ago. She is a very energetic and enthousiastic child. Such a site is very interesting,thanks for t e info on vest. We need information, especially to compare treatments in France and in the US. Lots of love and courage to you Tanner.

Misty Warner - 04/18/00 20:48:04
My Email:mwarner@acbcoop.com

Comments:
I think that it is fantastic that you set up this website for your son. I just lost a very close friend with the same disease. his outlook was very bright towards life. And when I see the courage that these children and adults exert everyday I know that i is a gift to know people with such strength.

Nicki Fridley - 04/18/00 20:35:16
My Email:bobbinicole@hotmail.com

Comments:
I think your website is fabulous. My cousing is 15 and has Cystic Fibrosis. I am doing my college biology senior research paper on CF.

Ann Parisien - 04/18/00 15:15:23
My Email:annp_74@yahoo.com

Comments:
This is such a beatiful site. Tanner, I hope they find a cure too. This is sent with prayers and hope for you to get better.

Lindsey Melcher - 04/16/00 17:11:54
My Email:timman34@juno.com

Comments:
Hi Tanner I'm 8 years old your not the only person with CF I have it also. My prayers are with you. Lindsey Melcher

becky cook - 04/16/00 15:18:30
My Email:TAZBFU2@AOL.COM

Comments:
YOUR LITTLE BOY IS A DOLL AND SOME DAY THEY WILL HAVE A CURE....

KRISTEN - 04/16/00 06:06:14
My Email:KRISTEN121985@AOL.COM

Comments:
HI, i wish the best for your son and just as well your whole family! I am 14 yrs old and I have Cf too.Living with it for this long is normal now! Tanner is a special gift for you! That is what my mother always tells me when i get upset about doing my med cines and taking away most of my freedom!Every night I thank god and say "Thank you for letting me live another night and let me live looking forward to the nights to come!"The best to you Tnner especially and you whole family just as well!!!

Robin Barnett - 04/16/00 03:02:13
My Email:Rbnbarnett@cs.com

Comments:
You have a very sweet little boy! All the best to you and Tanner. I have a niece (Whittney) who is 14. She was diagnosed with diabetes about three years ago. So now she has two things to deal with.(cf and diabetes) She is doing so well! I am so thankful. t sure is hard on her Mom (my sister). Pray for her and Whittney. Thank you.

Mechelle - 04/14/00 02:10:52
My Email:mechelle@grnco.net

Comments:
Tanner, I think you are very brave. My son who is 5 also has cf and is doing really well.

Nichelle - 04/12/00 19:15:41
My Email:sk8erL07

Comments:
I thought it was cute !! i like it a lot I also have Cf and Im almost 14 years old The docter sayed I would only lie antill I was 3 And I lived longer then that

Angela - 04/06/00 16:18:05

Comments:
I have a daughter with cf.. she will be 5 in June. She is doing okay right now. She has not been quite as lucky as you. She has had way too many pnuemonias to count, but is doing well on all of her new medication. I love to hear such happy stories. Good luck and God Bless you.

Kim McKiernan - 04/05/00 22:14:52
My Email:hndztat2@hotmail.com

Comments:
Our son was just diagnosed with cf and I want to hear good stories like yours. I am so glad for you that you are healthy and doing well with the treatments. Logan is 6 and has been pretty lucky, he hasn't had lung problems and we hope to avoid that...he mostly has digestive problems and will be taking enzymes soon. Any advice you have would be welcome! Kim

Angela Harsh - 04/03/00 20:46:43
My Email:tharsh1@hotmail.com

Comments:
this is a really sweet site and im doing a report and i will include this site

keena bauer - 04/02/00 20:20:21
My Email:keena_95@hotmail.com

Comments:
Hi there! My name is Keena Bauer. I am a 23 year old woman with CF. I saw your web page and wanted to tell you I think it's wonderful and wish your family health and happiness! Keena Bauer

keena bauer - 04/02/00 20:19:50
My Email:keena_95@hotmail.com

Comments:
Hi there! My name is Keena Bauer. I am a 23 year old woman with CF. I saw your web page and wanted to tell you I think it's wonderful and wish your family health and happiness! Keena Bauer

Gillian - 03/30/00 14:55:46
My Email:pacey@sympatico.ca

Comments:
When I read about children with cystic fibrosis it makes me want to cry. It is so sad to see such young lives suffer. I hope your son has a long and healthy life. I'll be praying for a cure for you!

Amanda Stainbrook - 03/28/00 00:15:46
My Email:a_man_duh003@hotmail.com

Comments:
I like the new things. Wendy, e-mail me. Love you all, Amanda

Phyllis Krug - 03/27/00 00:42:28
My Email:pkrug1@aol.com

Comments:
I work for a teacher and his baby girl possibly has CF, she goes for the sweat test this week. I am trying to gain knowledge on this disease and happened onto your web site. To say that you touched my heart would be putting it mildly. Good luck to you and your gift from God parents!!!

Jenn - 03/23/00 13:58:16
My Email:starr_007@hotmail.com

Comments:
Your site was very interesting I am doing a project of CF in school and also I had a cousin die of CF about 3 years ago. I thought that this would be a good project to do since I have experienced it. Your site helped me find more information! Thank you and good Luck!!!

sue nolan - 03/22/00 21:38:12
My Email:nolan.sj@gateway.net

Comments:
our son Joshua was picked up on a new born testing in Colo. He is now 11 and doing well. We have had our bad times but the good times are so very good we are so blessed and God Is answering our prayers for a cure!!!

sandra kelley - 03/22/00 19:29:50
My Email:shepard@midcoast.com

Comments:
I have just found out that my nephew may have cystic fibrosis. It is very scary for me. Your web page is beautiful. I just hope that my family can be as supportive to him as you are to your son. Best of wishes. And my prayers are with your son and yo r family. Thanks for the encouragement, Sandra Kelley

Heather - 03/19/00 04:13:25
My Email:dncrdreams@aol.com

Comments:
Tanner, hey there, my name is Heather. I am 16 and I am doin a research report on cystic fibrosis for school. Im sorry to hear u have it and I know you must have a tough life but stay strong and remember that everything happens for a reason. In fact my best fri nd like you has cystic fibrosis and she is 13 and she is a great person with a great personality and Im sure ur the same way. Feel free to e-mail or im me ever if u need a friend. I'll keep u in my prayers and God Bless. -<3- Your Friend -<3- Heather

Heather - 03/19/00 04:08:43
My Email:dncrdreams@aol.com

Comments:
Tanner,

elizabeth - 03/18/00 19:49:10
My Email:silver4099

Comments:
my son also has cf we found out when he was 4 month old he is now 2 years old and your website touched me you put into words how i have been feeling for so long they are special in their wonderful way may GOD keep blessing you i sure enjoyed your site

Heather Schafer - 03/17/00 19:01:54

Comments:
Hi Tanner You will never guess but i have cystic fibrosis also!!! It sucks having to take all that medicine and do all those treatments doesn't it? But, I try to live life to its fullest. I am 18 years old. I have been in a car acident and fractured my back. I have had to have two surgeries on my back. When the acident happened I almost died. I've strugged alot of my life. But, I've had many of f n times. I don't have email yet but I will get an address so you can email me back. Talk to you later. Nice meeting you.

Darsea - 03/11/00 04:07:11
My Email:darsea_05@excite.com

Comments:
Heah Stainbrook Family, This is Darsea Korte. I know that Olivia and Wendy and Kenzie know me, but I don't know if Tanner does. Well, I thought that your page was very sweet. Good luck on finding the CURE!!!

Heather - 03/10/00 22:35:49
My Email:hmoots

Comments:
Vey touching pages. My niece just found out her 10 day old daughter has cf.I am surfing the web for info! Want to help her any way I can! Heather

Amy Schmidt - 03/01/00 05:14:35
My Email:schmidtp@accessus.net

Comments:
Thank you for this wonderful page. My daughter, Olivia, was diagnosed with CF at 6 mos. She is now 5 years and doing fairly well. I saw a bumper sticker at the time she was diagnosed that read "Expect a miracle" and I do. A cure will be found!!

Stewart Family - 02/24/00 20:44:34
My Email:our@locstat.freeserve.co.uk

Comments:
HI! We enjoyed reading your webpage expecialy the footsteps in the sand. Our son Tom is thirteen years old and was diagnosed with C.F. atthe age of one. He too has a vascu/port and recieves hom iv therapy. He attends a C.F. center in Dorset County Hospita England which is about fifteen miles from our home we are very lucky he has an excelent medical team last year Tom developed insulin dependent Diabetes due to steriod treatment for his C.F. but as usual he copes with this tremendously and is an inspirati n to all who know him. We would love to hear from enyone with similar experiences. Our best wishes to the Stainbrook Family.

Stweart - 02/24/00 20:29:03

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Uncle Dan and Aunt Sue - 02/22/00 00:17:01
My Email:sasha 11@bright .net

Comments:
Tanner, God bless you, and he will keep you in his loving arms as long as you trust in him and have faith in him. Just remember, all things are possible in our Lord Jesus Christ. He is still in the healing business if you call upon his name in faith. We l ve you.

Mary Ann Duling - 02/19/00 23:04:42
My Email:maduling@bright.net

Comments:
Tanner It was great to meet you on your website. I'm Jacob Ellerbrocks grandma and I enjoy meeting Jacobs friends. Bye

Shannon - 02/13/00 22:41:18
My Email:MiniMiaGirl9

Comments:
your information on CF has helped me a whole lot with my school project. I hope your little boy gets better! Shannon age 11

lynn d. and j.d. - 02/13/00 18:07:42
My URL:http://jacer 36
My Email:feb 13,00

Comments:
hello, my name is lynn and my sons name is jay. jay was diagnosed with c.f. last feb.and i wanted to say that everything that wrote i can relate too and i just wanted to say how beauitful your file was! i have been feeling pretty alone lately with this disease and after reading your file so ehow i just don't feel so alone. thank-you for sharing your story it helped. take care and i hope for the best for your family. lynn

Helen - 02/12/00 21:55:01
My Email:helen@clan-grant.com

Comments:
Your internet pages are absolutly fantastic, I have not got cf, nor has any of my friends or family. I am very interested in finding out about cf as I want to be a nurse when I leave university. Thankyou for helping me with my dreams. Helen age 18 years from England

Bob and Linda Derr - 02/12/00 11:50:31
My URL:http://www.pacfi.org
My Email:bobderr@sunlink.net

Comments:
Keep those dreams for Tanner alive and keep doing what you're doing as a family. Tanner definitely has a spirited personality!

Vannessa - 02/09/00 20:12:02
My URL:/cgi-bin/geoplus_apps/ans_entry
My Email:vannessac80@hotmail.com

Comments:
Hey, I really enjoyed looking at your web page. And you know what?? I really admire you for being sucha brave little boy! Keep it up, kid. And good luck!!!!

Vannessa - 02/09/00 20:06:47
My URL:http://www.geocities.com/Heartland/7820/olivia.html
My Email:vannessac80@hotmail.com

Comments:
Hi, my name is Vannessa. I live in Ecuador and I am doing a research project on Cystic Fibrosis. So this is how I found your little brother's web page. I think it is relly neat, I guess you really have a good time with Tanner, he looks like such a grea kid. So anyway, I think this page was really neat! Good luck!!!!

JENNI - 02/06/00 04:14:52
My Email:UTF.@ATLANTIC.COM

Comments:
WOW! THAT IS SO AMAZING!I AM 16 LIVING IN FLORIDA AND DOING A SCHOOL PROJECT ON CF AND NEEDED SOME INFORMATION SO I WAS SEARCHER AROUND AND COULDN'T BELIEVE WHAT I CAME ACROSS. LOTS AND LOTS OF LETTERS JUST LIKE YOURS TALKING ABOUT CF. I AM SO THANKFUL I M HEALTHY! I REALLY DON'T THINK ABOUT HOW MANY PEOPLE ARE SICK AROUND THE WORLD. IT'S SO JUST UNBELIEVABLE!! THANK YOU SO MUCH FOR SHARING I WISH YOU AND YOUR FAMILY (ESPECIALLY YOUR BRAVE LITTLE BOY) HEALTH AND HAPPINESS IN THE FUTURE. LOVE~ JENNI P.S. E-MAIL ME BACK AND LET ME KNOW HOW YOUR LITTLE BOY IS!THANX

JENNI - 02/06/00 04:13:53
My Email:UTF.@ATLANTIC.COM

Comments:
WOW! THAT IS SO AMAZING!I AM 16 LIVING IN FLORIDA AND DOING A SCHOOL PROJECT ON CF AND NEEDED SOME INFORMATION SO I WAS SEARCHER AROUND AND COULDN'T BELIEVE WHAT I CAME ACROSS. LOTS AND LOTS OF LETTERS JUST LIKE YOURS TALKING ABOUT CF. I AM SO THANKFUL I M HEALTHY! I REALLY DON'T THINK ABOUT HOW MANY PEOPLE ARE SICK AROUND THE WORLD. IT'S SO JUST UNBELIEVABLE!! THANK YOU SO MUCH FOR SHARING I WISH YOU AND YOUR FAMILY (ESPECIALLY YOUR BRAVE LITTLE BOY) HEALTH AND HAPPINESS IN THE FUTURE. LOVE~ JENNI

CAROLY FRONDORF - 02/06/00 03:48:01
My URL:http://mike_fronforf@fuse.net

Comments:
what a beautiful son you have.We go to cincinnati childrens hospital our daughter was dx with cf at 4ys old,she is 7 now and doing great. I know a cure is going to come in their life time. God bless your family.SOMEDAY CF WILL STAND FOR CURE FOUND!!!!!

CAROLY FRONDORF - 02/06/00 03:47:15
My URL:http://mike

Comments:
what a beautiful son you have.We go to cincinnati childrens hospital our daughter was dx with cf at 4ys old,she is 7 now and doing great. I know a cure is going to come in their life time. God bless your family.SOMEDAY CF WILL STAND FOR CURE FOUND!!!!!

dixie thomas - 02/04/00 03:31:48
My Email:Jaimierob@dellnet.com

Comments:
You are such very brave and strong people. I came to you web site to look up information on Cystic Fibrosis and your words touched my heart. I started crying. May the Lord above bless the rest of your lives with eternal happiness. Thank You for enligh ening me on your heartache. I'm so sorry.

Melissa Rowley - 02/03/00 18:36:11
My Email:melissa.rowley@wellstar.org

Comments:
Your Web Page was wonderful. My 7-month-old daughter has been ill for several months. We have been on every medication and been hospitalized a few times. She has had several upper respiratory infecitons, RSV, coughing, wheezing, and recently had phenom na. For months we were not getting any answers. We have finally changed Pediatricians, which sent us to have CF test. That came back with a score of 31. I his eyes that is a CF score. After meeting with the Pulmonology Specialist he was not happy with that score, as well her platelet and white blood cell count was down. He is sending us to a Children's Hospitals that Specializes in CF patients. I feel for you and your family. This is our first child; my husband and I hold her at night and just cry. I had a very rough pregnancy, and now this. We pry everyday things work out. We tell ourselves god gave us this special child for a reason. Do you remember your son's score on the CF test? As well, did your son start on a medications as soon as you were given the news?

Tony Rypma - 02/03/00 03:59:47
My Email:trypma@venus.net

Comments:
Really enjoyed your site, very touching. As a father of a cf child it does my heart good to see how special our children are to us.My son is 14 now.We live near Seymour Indiana,and go to Riley in Indy.Recently Nathaniel received the vest,what a blessing!

Danielle Copeland-Bethke - 02/02/00 05:10:21
My Email:danielle.m.copeland@diversified.com

Comments:
Hi! Enjoyed your web page. My 5 1/2 month old son was tested last week for CF,and we are nervously awaiting the results. In the mean time, I am trying to gather as much info on CF that I can. He has had a chronic cough/wheezing for almost three months, an recently has had pretty nasty diarrhea every day for a week, at every diaper change. Say a prayer for him! His name is Donny. Bless you and your family, and keep up the positive attitude and never-ending support for your son!

Elaine Matherly - 02/02/00 02:18:06
My Email:dematherly@cs.com

Comments:
Tanner, You are a beautiful little boy. I hope that you will stay healthy. I will be praying for a cure for C.F. I will also be praying for you little man. Take care of your Mommy. We mommies need lots of hugs.....

Sarah Lewis - 02/01/00 15:36:13
My Email:sarah.l@mailcity.com

Comments:
This is an awesome as well as heart wrenching web page. Please know that my thoughts and prayers are with you and your son.

jackie davenport - 01/30/00 04:08:55
My Email:casperamsn.com

Comments:
hey its me jackie bryces mom. we just got a new computer . we also got registered to get bryce the vest. im so excited.

Melody Pfaff - 01/26/00 19:32:24
My Email:mpfaff@usd384.k12.ks.us

Comments:
I have a seven year old daughter with cf.

Regina Samulski - 01/26/00 00:04:30
My Email:gina56039542aol.com

Comments:
I just want to say that your web page is beautiful! Regina

Deb Jackson - 01/23/00 19:47:24
My Email:litldebit@aol.com

Comments:


cindy chvarria - 01/20/00 15:50:12
My Email:www@hotmail.com

Comments:
My little nephew has cf he is 3 years old, I hope soo God sends the cure.

Ian Hagerty - 01/18/00 19:38:18
My Email:cc983056@janus.northatlantic.nf.ca

Comments:
Hey Tanner...keep going buddy,,,I have a nephew with cf and I am pretty confused by the whole issue,,,I love him the pieces and would do anything for him...I can relate to your situation...I am praying for you,,,IT WILL WORK OUT!!!!LOTS OF LOVE FROM NEWFO NDLAND/CANADA...IF YOU CAN, PLEASE DROP ME AN E-MAIL,,,IAN

Ryan Bollig - 01/18/00 17:06:46

Comments:
I have cf and battling like tanner is. Its hard but i put it that god made me to be special!!!! I wish i didn't have this diesese but it's not no ones falt!!!

B. Lambert - 01/13/00 23:23:05
My Email:Jameslamar@earthlink.net

Comments:
Beautifully done! What a lucky boy. Best wishes to your family---CF mom in Idaho.

- 01/09/00 03:12:54

Comments:
Beautiful pictures and story of a special child. My daughter was diagnosed at birth with CF and is doing very well. Life goes on with many wonderful days that I never imagined when we first heard the diagnosis of CF. My husband and I were also married on May 5th but in 1986. Continue the faith and h pe in a cure.

- 01/09/00 03:02:41

Comments:


Vickie Goedde - 01/09/00 02:37:40
My Email:vgoedde@bright.net

Comments:
Tanner, You're very lucky to have a Mom and Dad and sisters that care so much for you! Remember that all of us care deeply about you and your family and would do anything in the world to help you out anytime! Remember that we are praying for you and for a cure. Keep that cute smile of yours always and be as ornery as ever for your Mom! Love always, Bill, Vickie, Dawn, Matt, and Nate p.s. Wendy, If there is ever anything we can do for you, please don't hesitate to ask! We feel you and yours are a part of our family! Vickie

Dawn Goedde - 01/09/00 02:02:00
My Email:dgoedde@bgnet.bgsu.edu

Comments:
Hi Tanner!!! You are very special to a lot of people including me!

Jenn Fredericks - 01/08/00 16:59:55
My Email:walker409@hotmail.com

Comments:
Your page is wonderful. I have a 5 month old son, who's been having some pretty serious porblems with breathing (asthma), and has a lot of mucus which he is unable to get up. If this round of antibiotics doesn't work, the next step is testing for cf. N edless to say I am extremely worried and your web page about your son has helped me have a little faith. Thank you.

Lisa Padron&Family - 01/05/00 23:00:14
My Email:padron4@bright.net

Comments:
Wendy, you have a beatiful son. He looks just like you. You are a very strong person to have endured such much pain with Tanner. I envy you for having so much strength. Where there is a will there is a way. Keep up the fight!

Ray Stackhouse - 01/04/00 02:08:59
My Email:ray.stackhouse@tvguide.com

Comments:
Your Tanner is a beautiful boy. From reading what he's gone through already at his age, I can see that he's an incredibly brave and courageous youngster, too. My brother's son Sean (23 months)has cf, and my wife has two brothers who each have a child with cf, so we've become pretty familiar with the disease. My niece Molly (20 months) spent about two months in the hospital with complications but she's doing quite well now. My nephew Brian (also 20 months) so far has been able to avoid any problems that req ire hospitalization. I see what having a cf child entails, with all the medications and treatments and special care and attention that they need. If you were to look at them you wouldn't know there was any kind of medical problem. They sparkle with life, ove and laughter. They are three exceptional blessings, just like Tanner is. Everybody keeps praying for a cure, and God willing, someday our prayers may be answered. Thanks for reading this, I hope I didn't blather on too much about my niece and nephews. Keep fighting, Tanner, I love hearing stories about kids who don't let cf get them down. All my best, Ray Stackhouse

Chelsea Bohrer - 01/03/00 20:26:14
My Email:tweetie50@hotmail.com

Comments:
Hi. I really enjoyed your web page. I am a friend of your babysitter Kasey. She talks about you all the time. You sound like a really neat kid. Goodluck on finding a cure for your CF. Well bye! Chelsea :-)

Emily - 01/03/00 00:37:08
My Email:emilina17@hotmail.com

Comments:
I love your page. You seem to be the best mother ever. I hope they find a cure for tanner and everyone else out there with cf. Best wishes....Emily

deb - 01/02/00 02:47:24

Comments:
What a wonderful page. He will appreciate that so much when he gets older. I love it.

peggy - 12/31/99 00:00:35
My Email:pjvbooland@aol.com

Comments:
i have a 21 month old who was dx thismonth and your web was page was a great pick me up good luck to you and your family if you have a ideas for us feel free to e mail us ..

Chris - 12/22/99 17:42:20
My URL:http://members.accesstoledo.com/sstandiford
My Email:Pray4Michael@aol.com

Comments:
Dear Tanner! Thought I'd stop in again and see how you're doing. Keep strong, and have faith in God. Have a merry Christmas. Chris

Dana - 12/18/99 22:31:44
My Email:waterbug12.com

Comments:
Hi Tanner.I have a daughter that is 13mths.She was diganosis when she was 4mths.Shes doing very well and i hope your mom and dad is to.Its very hard for all of us.keep in touch

Marichi Turner - 12/17/99 21:56:24
My Email:marichi10@hotmail.com

Comments:
This is so sweet. I am a 20 year old female CF patient and was diagnosed at 3 mos. old. I know the trials of CF. Just live each day to the fullest-keep God part of it and pray one day we can all breath easier. Take care.

Andy Gee - 12/16/99 05:34:37
My Email:xig_26@hotmail.com

Comments:
Hey Tanner, I just want to say, that I think you are very brave living with CF. My name is Andy and I am 13 years old and living with CF myself. You might not be old enough to read this right now but, I just have to try to get my message across. You need to give our Mom confidence in you. Like when you're sick (especialy in your young age). And your mom gets realy worried, almost in tears, you have to tell her "Mom, I'm gonna be okay," "I promise..." And you have to stick to that promise for as long as you live. ou have to keep your mom's words with you. Because she knows you are strong enough to stay healthy. sincerley, Andy Gee

Brandi - 12/16/99 04:01:05
My Email:lilone6721@yahoo.com

Comments:
I really admire how you and your son have gotten through all of the trials and troubles of this disease, and I just wanted to send my heart out to you and your son, and just let you know that there is someone out there who really cares.

Ginger - 12/16/99 00:19:22
My Email:BLAKE418@webtv.net

Comments:
Hi Tanner. It was nice to meet you. I have a little boy who is 2yrs old with cf. He has the vest too. He is doing very well. I believe the cure will be found soon. Hope you have a very Merry Christmas!!!! Love, ginger

Dean Sleevi - 12/15/99 19:14:12
My Email:DSleevi@email.usps.gov

Comments:
Thank-you for sharing your feelings and events. I have a daughter, just about 13 with CF. She was diagnosed at 11 months, and as you already know, there is a tremendous amount of emotional luggage that starts to pile on as the days and weeks go by. Our daughter is doing very well, she has played in girls basketball, in studying Karate (5 levels already achieved!) and resists anything that suggests she is "incapable" of attempting the challenge. The most significant thing I've learned from her is how sh is keenly aware of her physical state. It would appear that you will be encouraging your son to share the same things with you. I trust in the Lord to do his perfect will in this issue and I'm sure you folks will also. God Bless.

holly - 12/12/99 22:23:09
My Email:sweetiepies69@hotmail.com

Comments:
hi I visited your sight because im doing a project about this disease. I hope your one of the lucky ones who live a great life until your 60 and do what it is your goal and dreams are. I dont know what its like because i dont ahve the disease but what i have learned is that it is very hard doing certin things. i hope you have a great holiday and a very special merry christmas you desirve it. holly

Michelle and April - 12/10/99 01:32:40
My Email:jmbanitro@aol.com

Comments:
I loved it!! I just found out today that my friends 5 year old has CF.This gives people a lot of hope. Thanks!!!!!!!

Mike - 12/10/99 00:28:34
My Email:mmcunn@aol.com

Comments:
God Bless you for sharing your story.

Emilie - 12/09/99 19:44:14

Comments:
Hi My name is Emilie I'm 3 years old and I have Cystic Fibrosis, my mom is writing this because I can't write yet. Nice page

Emily - 12/09/99 15:04:18
My Email:Chucki87

Comments:
Hi this is Emily. I am 14 years old and I am studying Cystic Fibrosis. I think that your guestbook is really cute. E-mail me! bye Emily

Matthew McLellan - 12/03/99 04:36:38
My Email:tim@oldmilltown.net

Comments:
I think your web page is really cool. Matt Yelm,WA.

Matthew McLellan - 12/03/99 04:33:04
My Email:tim@oldmilltown.net

Comments:
I thought it was really cool. Matt Yeim,WA.

Gena Major - 12/03/99 02:48:33
My Email:GMajor4@excite.com

Comments:
i wanted to say that your site is beautiful, my son is 3 and has cf it has b4en pretty easy so far, we have been blessed. i would love to make a page dedicated to him, but i have no idea where to start.....well good luck to you and your family, god bless ou , feel free to email me, i could use a mother to talk to during the rough times, thank you

Shannon Wyant - 11/30/99 20:53:17
My Email:sewcntry@farmwagon

Comments:
It was a wonderful Website!! I am a mother of a daughter, Holly. Whom was diagnosed with CF at 3 months. It sounds like we have the same story. Please, Tanner keep up the good work and God Bless. If you would like to write sometime or E-Mail, feel fr e. I would love to here from you. Holly is around the same age. She will be 3 May 7th. Address: 201 Walnut Arrowsmith, IL 61722.

Alisha - 11/29/99 19:13:24
My Email:Fairytayle@hotmail.com

Comments:
Great site!! I send you all the prayers in the world!! Keep up the fight!! Although I do not have CF, my brother Brandon did! He was and always will be my hero! unfortunately we lost Brandon this past Easter! Although I miss him terribly, I know that he is breathing easier!! Brandon's story is alittle unusual in the sense he was diagnosed at 19!! He lived a great life, never giving up. He died at 25 but his mark is what keeps my fighting to help fund for a cure!! You take care of your family, and continue to fight!! Tanner is lucky little guy!! Thanks again for the great web site!! Warm thoughts and prayers go to you and yours!!! Love, Alisha

Julie - 11/28/99 21:12:39
My Email:purple_gurl_1217@hotmail.com

Comments:
Hello, My name is Julie, and I too have CF like your son. I would be very interested to hear your story of his life. Please write me! Hugs, Julie

JodieNolan - 11/28/99 04:32:07
My Email:PeterJNolan.BigPond.com.au

Comments:
Hello to all your family, It is truely lovely what you have put together!!!. We have just received the internet and I was just having a look around as our daughter has CF, she is 6 months of age. We are from Twoowoomba, Australia, so it would be quite amazing the people you woul reach all over the world through your gustebook. Have a very special and happy xmas, regards, The Nolan family.

JodieNolan - 11/28/99 04:27:54

Comments:


Steve Tyson - 11/26/99 00:12:36
My URL:http://www.exec-group.com
My Email:steve@exec-group.com

Comments:
A wonderful, touching web page. Our son is 16 and has CF, we are so proud of him. Steve Tyson

Stephanie Franklin - 11/24/99 02:46:15
My Email:kayden@geotec.net

Comments:
Tanner, my son, Kayden, is 7 months younger than you and was diagnosed when he was 18 months old. He, also, will be getting the ABIVest in a couple of weeks. I hope he takes it as well as you since he cannot sit still either!

Lacey - 11/22/99 17:45:03
My Email:LBabydoll@excite.com

Comments:
Tanner, you are a very cute boy and I'm sorry that you are sick with CF. I recently had a very sweet 19 year old cousin die of CF. She was a great person. I hope all goes better for you. With Love, Lacey (16 years old)

Trisha Ramsey - 11/21/99 06:23:25
My Email:ANMJRAM@AOL.COM

Comments:
Hello, my name is Trisha. My brother Died This July 21,1999 of Cystic Fibrosis. This is a terrible disease that took my only brother and my only sibling. He was 21 years old. I love and miss him sooo much. I pray that there will soon be a cure. I will kee Tanner in my prayers. Check out my brothers web site at WWW.PUSH4Johnny.com Sincerely, Trisha Ramsey

Christi Mason - 11/16/99 03:40:47
My Email:masonc@citrine.indstate.edu

Comments:
I absolutley loved your website!!!! I have been dating someone very seriously for the past two and a half years, he carries cystic fibrosis. I know that this is the man I want to spend the rest of my life with, but it is very hard for me to look into th future, knowing that he may not be there. I want to have a family with him, but it is hard to commit to something like that when there is a chance he will leave the family. Your website made me realize God will someday send a cure and my boyfriend and our son will live life to it's fullest extent!

Allison - 11/12/99 01:43:02
My Email:alleymcc@bellatlantic.net

Comments:
My son was just diagnosed with CF in July. He is six years old. I was just checking things out and I saw your web. I decided to look at it. It is great. I wish your family well, and please , if you have any advice or good recourses let me know. we just got the vest a month ago! Thank you allison

Katie Aucoin - 11/11/99 21:35:58
My Email:JustSmily@aol.com

Comments:
Your web site was wonderful!! I am doing a report on Cystic Fibrosis in science and my teacher let me go online in our school library and I went to cf.com and I saw your web site and I apsolutely loved it!My friend that was sitting by me And I started crying!!It was so sad.Well Gotta Go!!

Cece Dodge - 11/08/99 02:54:12
My Email:egoodrich@uswest.net

Comments:
your wedsite for your son was very sweet my daughter will be tested for cf this week, seeing your son, gives me hope but makes me feel better not to cry but to wait and see the test results, thank you...

kathleen - 11/07/99 21:48:20
My Email:whitey_2000_99@yahoo.com

Comments:
hi my name is kathleen.my cousin has c.f shes only 5 and i pray for her everyday and i hope they'll find a cure for this horrible diease and i hope tanner will get healthier everyday

Brian and Amy Kidd - 11/05/99 23:38:29
My Email:amkidd@marathonoil.com

Comments:
Hi Tanner and family. Great website!! Tanner, just remember that anything and everything is possible and there is nothing that you can't do. If you ever need anything you know where we are. To many happy, healthy years. Brian and Amy

Ben Burry - 11/05/99 04:23:54
My Email:STEELHEADU@AOL.COM

Comments:
Hi Tanner!! It's about time your mom and dad sent me your webpage address. It is a terriffic site for a terriffic young man. I am gonna send it to all of my friends so that they can see and write to you too.

Ben Burry - 11/05/99 04:11:36
My Email:STEELHEADU@AOL.COM

Comments:


S Taylor - 11/05/99 02:25:50
My Email:Sltajt@aol.com

Comments:
Your website was just what I needed... It is uplifting, especially the angels and footprint poem. Thanks, A Newly Disagnosed CF patient, Stephanie, Age 25

Katie - 11/05/99 02:20:08
My Email:Smilelots@aol.com

Comments:
Your son Tanner is beautiful! The letter you wrote is incredibly touching. (Made me cry.) My favorite little boy (my friend's one-year old) had Cystic Fibrosis, too. I wish you all the best.

Mommy - 11/03/99 03:37:02

Comments:
I Love you Tanner

breanna - 11/02/99 15:50:36
My Email:Frog1606@aol.com

Comments:
Hi, my name is Breanna. I am doing a research paper on cystic fibrosis, and just by viewing your page, I was deeply touched. Before I got this paper assigned, I hadn't even heard of this disease. I was just wondering if you could send me some more informa ion on cystic fibrosis. I hope that I hear from you as soon as possible. Your son and family are in my thoughts and prayers! Thank you so much! Breanna


Nina Baiardi - 10/29/99 20:00:30
My Email:nenapr23

Comments:
I have a two year old cousin named Faith. Faith has CF too. I see your sons pictures and how much it reminds me of Faith when she was a baby. Faith was dignosed when she was almost eight months old. Doctors told my aunt that her brest milk wasn't giving aith enough protien. When faith went to the bathroom it was bail. Long Island Hospital in Brooklyn NY has been wonderful to us. it hurts alot to see her when she is sick but CF makes her who she is. Her mother gave her the right name. and i'm so glad to s e all the people out here who have faith. I love her so much. I wish your family the best of luck! (the email adress is a friends i dont have one of my own but I would like to here from you) thank you for this page! God bless your son and your family

ashley - 10/26/99 04:26:48
My Email:ashley924@aol.com

Comments:
I love your site. It is really neat. Tanner is a beautiful little boy. Hopefully they will find a cure for him. A cure is too late for many of my friends who had cf.

Kay Brady - 10/25/99 05:13:51
My Email:bradyh@prodigy.net

Comments:
Loved your wed-page, my son is 10 and has CF learned something about a vest will look into it. Anything to help him do his chest PT I'm for, thank you for the info. Our prayers are with Tanner! The Brady Family Port Orchard, WA

Tammy - 10/24/99 18:13:54
My Email:biggandt1@msn.com

Comments:
my son was 7 months old when he was diagnosed. he is now 7 years old. he does all the same things tanner does. this home page is absolutely beautiful

Deana - 10/22/99 01:48:39

Comments:
This is your cousin, I just want to tell you that I love you and that you are kept in my prayers,always.Just remember there is nothing to big for our lord to cure.He will never leave or forsake us.Look to him and he will give you strength.love you,Deana

Allyson - 10/21/99 00:05:34
My Email:allygator80@yahoo.com

Comments:
i really enjoyed your website. It was a very touching story. I choose CF as my research topic in my biology class and your cite helped me out alot, thank you very much

A.M. - 10/19/99 22:13:48

Comments:
I am a 17 year old with a cousin that suffers from cf. She is very positive about her disease and lives life to the fullest extent. Although, she hasn't had the best of luck, she still keeps fighting. She is now 11 years old and was diagnosed at 2 mont s old. She has had to have a clostome due to a bad bunch of enzymes, but our family has learned to deal with the disease and are continually here for her and her parents. Best of luck in the future and God Bless!!!

Barbara - 10/14/99 19:11:52
My Email:bwiles@cheshire.k12.ct.us

Comments:
This is a wonderful web page....Thanks for sharing it with all us other families dealing with CF.

Donna - 10/14/99 17:53:09
My Email:dcowfer@yahoo.com

Comments:
You are a brave boy... I'm praying for you, your mommy and daddy and the cure everyday

Uncle Alan - 10/13/99 21:25:10
My Email:kreidler@bright.net

Comments:
Cool page little guy! Don't let your dinosaurs eat you up! Make sure that you play your guitar a lot and make sure that the volume is turned up all the way! GO BUCKS! Beat the team up North!

Regina Samulski - 10/11/99 15:20:47
My Email:don't have one!!!!!!

Comments:
I just wanted to say hey to everyone who has to deal with all of this stuff!!!!!

Amanda Stainbrook and mom and Kristen - 10/10/99 18:31:25
My Email:croy@gurlmail.com

Comments:
Hello, There are some really cute pictures on here. Say Hi to Tanner for us. Love, Us

Anne - 10/10/99 01:47:45
My Email:annesar@start.com.au

Comments:
Hi Tanner, I have a six year old grandson,Jacob, who, like you suffers from CF. Fortunately he has kept very healthy so far ,thanks to all the work his Mum,Karen, does with physio etc. He also finds that he would rather be running and playing than having nebulisers and physio but I think that since he has started school he has become more patient with the whole bit. Keep fighting and hoping , as we all do , for that miracle cure. Anne Sartori Tamworth, NSW Australia

Penny howard - 10/09/99 13:58:38
My Email:65roses@mciworld.com

Comments:
I was wonderful! You made me cry and toke my same thoughts right out of my head.

Penny howard - 10/09/99 13:58:18
My Email:65roses@mciworld.com

Comments:
I was wonderful! You made me cry and toke my same thoughts right out of my head.

Curtis Ausmus - 10/09/99 03:14:40
My URL:http://www.geocities.com\Heartland\Shores\9443
My Email:dla34@hotmail.com

Comments:
Hi Tanner I sure like your web page mine is still being worked on well I sure hope you stay healthy and well.I'm doing pretty good I haven't been sick for a long time.I have a cousin with C.F and he is 27 years old and he told me what he does to keep goin healthy is eat lots,exercise and take care of yourself by taking all your medicines.Well I hope you check out my web site oh just to let you know I am 6 years old well bye for now.

Jennifer Kling - 10/09/99 01:41:52
My URL:http://www.geocities.com/Heartland/Fields/1846/
My Email:jenkling@skyenet.net

Comments:
Hello, I must say that this is by far the most touching personal web site that I have seen so far. You did a very good job of putting this together! I wanted to say thanks for visiting my page and signingthe guestbook. It really means a lot to me when eople take the time to do that. I wish you all the luck and happiness that you can handle, and you will always be in my prayers. Your sone is a beautiful little man!

James Vilas - 10/08/99 19:28:23
My Email:jvilas@ix.netcom.com

Comments:
I think that what you've done is beautiful and touching. I too am a parent of child with CF. He too was the little boy that I prayed for and he is everything that I ever wanted. He will be two at the end of the month and was diagnosed when he was thre months old. Put on the website how old Tanner is now and when he was diagnosed. i will go back "through the gates" to see more. My wife and I are like you, " we have to keep him healthy and minimize the damage until there is a cure". I hope that you b th get involved with fundraising and spreading the word around about CF. The more people that know about it the better. May God bless Tanner's soul and purify his body. I ask that every night while placing my son, Miguel into his bed.

brooke hewitt - 10/08/99 13:48:19
My Email:oke15@excite.com

Comments:
i was looking up stuff for school on CF and i found your website. it has let me get information and i have learned a lot. you have many creative ideas on how to tell me and others about it. great job. i am 15 and in 10th grade. thanks again.

Marty May - 10/08/99 02:19:43
My Email:mamay0@coxnet.org

Comments:
Great web page! I have a son with CF who is 28. He was diagnosed at 11 months. I have so much to say but will make it brief. He has lived a wonderful and full life. He has never let it hold him back. He is a champion horse back rider and competiter. He will be waiting for a set of new lungs for transplant soon. He is just not as able to do what he wants now and wants to get on with life so has decided that the next step for him is a transplant. Everyone: hang in there!

Chris Hipsher - 10/05/99 21:01:08
My URL:http://members.xoom.com/mstandiford/index.htm
My Email:ReggieB123@aol.com

Comments:
Tanner: I'm a volunteer at the Toledo Children's Hospital. I met you a couple weeks ago. I hope they find a cure!! God Bless you.

Jenny - 10/05/99 19:09:57
My Email:bellesaurm@juno.com

Comments:
My brother and sister have cf. They go in the hospital at the same time about every four months. Jessi just got a port put in. They aren't as bad as I thought they would be. Joe was 18 months old when diagnosed and Jessi was 6 months old. I know how you f el. Joe takes about thirty pills a day when he is healthy. He doesn't always want to do his treatments. Don't let anybody hold you back. Joey is on the varsity football team.

Kathy - 10/05/99 11:24:29
My Email:Kshacket@us.ibm.com

Comments:
Beautiful Website. Best of luck with your life, and may it be a happy long one.

jackie davenport - 10/03/99 21:29:40

Comments:
hi its me again! just got done introducing tanner to my parents they think hes a doll

Jeri and Carol Cardwell - 10/03/99 20:10:54
My Email:cardjell99@aol.com

Comments:
Hi I'm Jeri I'm 12 my mom Carol has cf we are writting you to give you hope for a long life my mom is 39 she is doing well we work hard everyday w/ lung treatments, oxygen, and medicine to keep her healthy I would like to here from you to see how you are oing. Jeri cardwells Email scjethfa@aol.com and my moms Carols is cardjell99@aol.com

Amy & Erik Brown - 10/03/99 01:58:02

Comments:
We have a 4 year old foster son with CF

Erica - 10/02/99 18:43:03
My Email:denverredhead@aol.com

Comments:
I am doing research on cystic fibrosis, and yours is by far the best website I've been to so far. You provide so much wonderful information. Thank you and God Bless.

Cathy Grasinger - 10/02/99 05:15:42
My Email:cojco

Comments:
I too am a mom of a son w/ CF. His name is Cole and will be 3 in February...he has been doing very well and I am so thankful for the medicines and all the research they are doing for our kids!! You have a beautiful page, it really helps to see other parents out there going thru the same things.. and are hanging in there!!! God bless you and your family, Sincerely, Cathy Grasinger

Cathy Grasinger - 10/02/99 05:15:23
My Email:cojco

Comments:
I too am a mom of a son w/ CF. His name is Cole and will be 3 in February...he has been doing very well and I am so thankful for the medicines and all the research they are doing for our kids!! You have a beautiful page, it really helps to see other parents out there going thru the same things.. and are hanging in there!!! God bless you and your family, Sincerely, Cathy Grasinger

Nissa Ericson - 10/01/99 15:29:53
My Email:ericson@svs.net

Comments:
Yours is the best personal web-site I've ever been to...I'm doing a report on cf and wanted first hand information. Thanks! I'm very impressed :)

M.Miller - 09/29/99 14:51:30
My Email:Moe638@hotmail.com

Comments:
Your webpage is terrific! My niece is 14 and has CF. They didn't diagnose her until she was 2. I think I know a lot about CF now you have taught me some more THANKS!

Tamea - 09/29/99 07:38:43
My Email:shimmer_t@hotmail.com

Comments:
Reading your page and others like it helped me learn more about a disease that a friend of mine died from....thankyou very much

Jaime - 09/28/99 05:12:01
My Email:speckles123@aol.com

Comments:
Cool web page... you sound like a good big sister, I am a big sister of a CF kid, too. She just turned 4 years old, her name is Mikah. She is also blonde haired, blue eyed, and very energetic. She keeps us busy and on the run all the time. She is very happy even when she is sick. I haven't minded helping with any of her treatments. The only time I didn't want to help is when we had to do at home suction treatments. That was gross... and made Mikah mad and she cried alot. She doesn't have a vest yet She has a very good doctor.I am in the 7th grade. I have a brother, Tyler, who is in the 5th grade. Mikah thinks she's as old as us. She is very smart and takes her disease more easily than any one of us... she knows she can do anything and is willin to try anything.. she just has to stop to do breathing treatments or take medicine sometimes. I prayed for a little sister, and I got one. I am now praying for a cure for Cystic Fibrosis. It will come. Talk to you another time!! Jaime

- 09/28/99 04:51:18

Comments:


Ciji Smith - 09/26/99 21:53:25
My Email:c_s_100_21@yahoo.com

Comments:
To Tanner and Wendy, I came to know about this web page when I had a paper to do on enzyme related diseases. I don't know anyone with CF but reading this web page help me to learn more about CF. A cure will soon be avaible. May God bless you and keep you and our family safe for ever. Don't forget to keep the faith. Wendy this web page is a very good idea it helps people to learn more about CF. I will keep your son and your family in my prayers. 15 year old student

Kasey - 09/26/99 20:23:39
My Email:kaseyomighty1@hotmail.com

Comments:
tanner, when I first babysat you, I was very worried. But now that I know you, yo are so awesome and upbeat and ver postive. I will never forget you, and you are very fun to baysit for. Love you always, Kasey

Danielle - 09/26/99 19:25:25
My Email:love_flirt_99@yahoo.com

Comments:
Dear Tanner, Just keep your faith in GOD and you will be a strong little boy! My boyfriend doesn't like his treatment either! He wont take his oxygen with him! You are not alone and if you would ever like to talk I will be here for you! I love you! Lots of Love Daniel e.

Danielle - 09/26/99 19:13:50
My Email:love_flirt_99@yahoo.com

Comments:
That is a beautiful page! My boyfriend and best friend both have cf! I often cry to but I know that GOD did it for a reason! If you ever need to talk you have my e-mail! Please give your son a hug for me! I love you guys and know that everything will be ine!! Love always Danielle

C.Dillon - 09/26/99 13:53:54
My Email:unfedfish@hotmail.com

Comments:
i thought that this was a relly great page.i am a sixteen year old girl and during the summer i look after a young boy with CF.i have become extremely attached to him but i always worry what will happen because of his CF.i don't know very much about it.t anks for helping me understand more. Claire

Sandra Pack - 09/26/99 04:43:46
My Email:dakota95@sabinenet.com

Comments:
Tanner, I really enjoyed your story on cf. I have adopted my 4 year old grandson and he was diagnosed with CF the day before his 4th birthday. We are still pretty new at all of the treatments and medicines. When that wonderful cure is found we can all rejoice. You will be forever in my prayers. Good luck in life and may God bless you.

McKenzie - 09/26/99 03:12:31

Comments:
I love you. You are the best brother I ever have. The best brother in my entire life. I hope you don't get sick. I hope they find a cure for tanner. And they will always love you.

Oliva - 09/26/99 03:09:25

Comments:
Dear Tanner, I hope you are feeling better> I just wanted to tell you I love you. You are the joy of my life and you have to stop growling so you do not go back to the hostipal. I just wanted to tell you are the wildest and best brother anyone coul;d ever have. I love you Oliva

Tommy Meeks Jr. - 09/25/99 22:41:43
My Email:TMeeksjr@webtv.net

Comments:
Hey Tanne. You have a really neat web page. I'll keep you in my prayers & hope with you that a cure will be found soon.

Sue Yoder - 09/23/99 19:15:09
My Email:smyoder@aol.com

Comments:
Tanner, Wendy, and Gary, Thanks, Wendy, for giving me the address for Tanner's web page. I enjoyed seeing it and will visit it again. Tanner, stay healthy and out of the hospital for a long time, although I enjoy seeing you while you're in and playing dinasours. Take care and stay in touch.

Diane - 09/23/99 11:40:58
My URL:http://www.geocities.com/nashville/7254
My Email:rgorham@airmail.net

Comments:
What a beautiful message of love, hope, and Faith! Such an awesome family filled with such Treasure! Thank-you for this website.. It is a Blessing. I will be praying diligently for your Family! Jesus Lives- Diane

Kaye Srader - 09/23/99 09:46:44
My Email:cynk@flash.net

Comments:
Hi Tanner, I am a grandma of a sweet little boy named Caton who is also 3 yrs old and has CF. You are so blessed with a mommy and daddy that love the Lord and love you. Caton is our little miracle too. He has had two tummy surgeries but is a happy, ch nky little boy. Maybe I can send you a picture on the e-mail soon and you can have a "puter pal" that loves Jesus too. I will pray for you and your mommy and daddy. Hugs from Gran!

Amber Sheffield - 09/22/99 12:05:24
My Email:sheffieldak@yahoo.com

Comments:
We just found out that my cousin's baby girl has CF. I am just wondering what to expect. This has been a big shock. She is three weeks old and still in the hospital but seems to be doing great.

Luann - 09/21/99 13:05:05

Comments:
Wendy: Kim showed me Tanner's web site. It's wonderful what you have done. He is a very special little boy!

Kim Reno - 09/20/99 14:39:55

Comments:
Great web site Wendy, You did a great job!! Kim Reno

Kristy Speck - 09/20/99 06:33:25
My Email:Speck3turn2@aol.com

Comments:
I have a 4 year old (just turned 4, 9-7), blonde haired, blue eyed, ornery CF child as well... (just female)... diagnosed since 11-95--no major cf-related surgeries.. or hospital stays...We thank GOD daily for that!!!! Weight is a slow process...lungs doi g well, sinuses...well that is a monthly occurrence.... We live in a town of under 3000 people and so happens that we had 3 kids associated with this town with CF--- my little one, a little girl a few months younger than mine(father raised here,her grandm ther still lives here) and a 13 year old that passed away in August with major liver problems --Thank goodness these little ones are filled with vinegar, for it helps them cope with the set-backs...sometimes better than us !!! Enjoyed the web site...

Tralynn Troia - 09/19/99 01:49:06
My Email:wttroia@aol.com

Comments:
My daughter has CF. She is three years old. Please respond.

rebecca - 09/13/99 13:16:59

Comments:
Love your Graphics, and how you did the pictures. It was just amazing

DEanna - 09/08/99 05:10:00
My Email:shmoofin@yahoo.com

Comments:
I am 27 and very healthy for someone with cf. there is so much hope for people with cf. it is only a matter of years before a cure is available,just have faith and stay healthy. good luck

anneliese, RN - 09/06/99 10:07:17
My URL:http://caring4you.net
My Email:anneliese97@yahoo.com

Comments:
Thanks for stopping by my site. Your site is wonderful. ...bought a tear to my eye. God bless!

One More Time--Again

We have never met
yet, I look for you each morning.
We have never met
yet, I have got to tell you my story.
~~switch the power on---the screen a hazy green~~

Let's see, what do I want to tell you?
I can tell you anything--
Something cheerful--
Something sad--
For you will help me through.
~~softly humming---pages loading---connecting--website found~~

Yes, each day I talk to you
about anything at all.
Together, we make up such a wonderful group.
Yes, most of the time--
we down right have a ball!
~~darn--no one is in the room, I check my ICQ~~

Things are very real
out here in Cyberspace.
A world no one understands
unless they visit this place.
Together, we laugh--
Together, we cry--
Together, we talk--
together, we celebrate!
~~mail---click---retrieving messages~~

Each day, we share our joys,
heartaches, troubles and pain.
We even tell of our personal lives
knowing that someone will listen
and from judgement refrain.

When I am having a great day,
you are there--
When I am having a troublesome day,
you are there--
We are here for each other
each day, every day--
we are friends.
~~the room becomes alive---the ICQ flickers---a message in Email~~

Yes, we have met my friends
and it is a beautiful friendship.
One that is not built on looks or rumor--
but on written words--
For it is these words that are windows
to our inner beings--
Yes, windows to our souls.

I look forward to each day
knowing that I will see all of you~~
ONE MORE TIME---AGAIN!
~~all is well with my world for my friends are here {{{HUGS}}} **smiles** all is well~~

copyrighted: no duplicating of this poem under any circumstances or form without first contacting
author at anneliese@cccnj.net. To contact the author click here.

Thats the wonderful thing about the 'Net-----friends~!

Vicki - 08/26/99 12:08:05
My Email:cyberfogie@aol.com

Comments:
What a wonderful group of pages to celebrate Tanner's strength and determination. Tanner is a beautiful child. I am the grandmohter of Ashley Anne w/cf(the Princess Page)and found you from your signature on her guestbook.

Michelle - 08/15/99 16:12:35
My URL:you'll get it soon (I HOPE!!)
My Email:MSchuma277@aol.com

Comments:
Hi Wendy! I just looked at all the pages--very nice! I just hope I can do as good a job on mine as Mary has done on yours. I am trying! I know you wish more people signed, so maybe I should go back and do it a few more times! LOL

Gretta - 08/06/99 14:15:17

Comments:
I am so touched!!You did a beautiful job.

tammie neal - 07/31/99 19:17:17
My Email:judy@caveland.com

Comments:
we enjoyed your page. please send me an e-mail, i have a son and step-daughter that have c.f.

ron, nancy , morgan - 07/25/99 02:52:44
My Email:none

Comments:
hi tannie, i'm T-rex! Wanted to let you know we love you very much! Hang in there! The cure is coming!

Shellyj - 07/25/99 02:44:57
My Email:russianmom@hotmail.com

Comments:
I am a 28 y/o female with CF. thanks for taking time to build such a touching site.

Tammy Morgan - 07/23/99 01:33:31
My Email:tmorgan@iceweb.net

Comments:
I visited your web page tonight July 22,1999 and it was such a beautiful and heart warming story and pictures I ever see.I have a daughter with cf and I know exactly how you feel hoping for a cure soon.Your son looks like hes doing well.My daughter will b 6 soon and just recently had surgery and had a j-tube placed to get a better calorie boost on her.Your web site was great.

LIBBY OBERHAUSEN - 07/21/99 18:56:31
My Email:none

Comments:
My friends have CF and some doctors think I have CF. Some words of advice just hang in there and you might be the one who finds a cure. LOVE ALWAYS, LIBBY O.

Brent Hendrix - 07/19/99 21:31:08
My Email:boilers@prismcom.net

Comments:
Tanner, I'm fortunate enough to know your Dad, because of working with him. I know the port is no fun because my wife had one of those for her chemotherapy 5 years ago. Hopefully, you will be cured as she has been. Good luck!

Cindy S. & girls - 07/10/99 02:44:35

Comments:


Mommy - 07/08/99 03:30:30
My Email:gwstain@bright.net

Comments:
Hi Olivia, I just wanted to to know how much I love you.. You are such a big helper when Tanner gets his treatments. I am so proud of what you have become.. You are the light of my life and I love you to infinity...

Chris Lehman - 07/06/99 17:17:42

Comments:
Great Job on Website. Good Luck in the future Tanner.

Lisa Bergen - 07/01/99 01:27:13
My Email:berlis42@prodigy.net

Comments:
Stay healthy Tanner!!! I hope a cure is found soon. My late husband had CF. He just died in January at the age of 27. Don't worry, I know a cure will be found in your lifetime. They are close!!! {{{{HUG FOR TANNER}}}}

Jacob E. - 07/01/99 00:23:55
My Email:mlellerbrock@health-partners.org

Comments:
Tanner, this is your buddy Jacob. I love your website!!I hope I can come and play with you soon. PS my mom, grandma, and aunts say HI. We pray they find a cure real soon!

Jenny - 06/21/99 18:12:35
My Email:JLSchramm@AOL.com

Comments:
Hi Wendy and Tanner, I love your web page!! You did a great job. Come visit me Tanner next time you have a Dr's appointment. Stay healthy!

04:12:35
My URL:http://www.geocities.com/HotSprings/Villa/9559
My Email:sandy_n_ant@geocities.com

Comments:
Thanks for visiting my page & signing my guestbook. Now it's my turn. What a lovely & beautiful tribute to your son. You've done a great job on your page. Keep up the good work.

Carol Miller - 06/09/99 02:24:29
My Email:cmiller@q1.net

Comments:
What a wonderful site you have. Good Luck in the future Tanner and stay strong and healthy!!


Phena Alley - 06/07/99 14:05:36
My Email:lymacbeth@hotmail.com

Comments:
Hi Tanner! I'm glad to see that you are a very happy and healthy boy. And you helped me a lot with my research paper that I'm doing for English thanks a lot. I hope that they find a cure soon so that you won't have to go through all those tests or surgeries again ev r. I hope to one day maybe help doctors find the cure because as I said before your web page has helped me find something I'm really interested in doing for the rest of my life for a career. Thanks again, Tanner!!!!!!!

Peggy Callander - 06/06/99 22:07:31
My Email:pegandchad@msmisp.com

Comments:
Wendy, You did a great job! I hope all goes well with Tanner. My prayers are with you. Peggy

Nikki Kline - 06/06/99 21:47:24

Comments:
Tanner, I hope they find the cure!!!!!!!

Heather - 06/03/99 00:46:01
My URL:http://home.earthlink.net/~ricswave/page12.html
My Email:ricswave@earthlink.net

Comments:
Hey everyone. please visit my site. I have CF and so did a friend of mine. that is until he didn't have to deal with it anymore. he died jsut a little while ago. i tired to make the website in time for him to see it but he passed only a day after i got it up & running. but you can still visit the site & comment on it & i'm sedning everyone's emails of support to his parents. so please stop by and drop them a line. thank you :)

Sue Manges - 06/02/99 00:10:51
My Email:smanges@wcoil.com

Comments:
Tanner, I really like your "page". I hope you continue to grow and stay a healthy, happy boy. May God bless you and your family.

Kati - 06/01/99 06:11:13
My URL:/Heartland/Cottage/8176/
My Email:katipickle@aol.com

Comments:
Nice site!
(((HUGS))) for Tanner :o)

Kati - 06/01/99 06:10:24
My URL:http://www.geocities.com/Heartland/Cottage/8176/
My Email:katipickle@aol.com

Comments:
Nice site!

Michelle and Cody - 05/31/99 04:49:14
My Email:MSchuma277@aol.com

Comments:
Hi, Tanner! My name is Cody, and I have CF too. I am only a couple months older than you (12-15-95), so we're both three! My mom is making me a homepage too, so pretty soon you can all see what I look like! I'm pretty healthy, but really skinny. I've had a sinus surgery, too (three of them). They're yucky, aren't they?! Hope you feel good forever!

Terry And Darlene - 05/28/99 16:02:10
My Email:tjkreidler@uswest.net

Comments:
Hi Stainbrook's

Ariella Thomas - 05/27/99 23:47:31
My Email:croyals@surfsouth.com

Comments:
I'm glad that you are doing so good, I am 19 months and have just recently been diagnosed with CF. My momma is trying to make things better for me so I won't have so many bad days. I appreciate your web page, you look heathly and HAPPY.

LaDonna - 05/26/99 20:48:21
My Email:lhoffman@brigth.net

Comments:
Tanner & family, Your web page is adorable. Kept up the good work. One of Your Grandma's Dip Sisters, LaDonna

Linda Rower - 05/26/99 02:48:23
My Email:spike48_@hotmail.com

Comments:
Hello, Tanner! You're looking good. Your Grandma's friend, Linda aka Snoopy

Grandma Sherrie Butler - 05/25/99 02:23:10
My Email:butler@bright.net

Comments:
Tanner is very special to Grandpa and me..we pray for a cure for CF everyday, and do our best to keep him healthy until that day arrives. In the mean time we just give him and his sisters all the love we can and enjoy each and every day as they come. T nner is our 'ornery' 3 year old blessing!

Mary - 05/25/99 01:31:49
My URL:http://www.geocities.com/Heartland/Plains/5526

Comments:
Now we do have a nice looking page going. Hi Tanner. Mary

Aunt Melissa + Uncle Charlie - 05/24/99 16:50:55
My Email:mbcb@netwalk.com

Comments:
To the strongest, little boy in the world!! We love you!

Suzy Frey - 05/24/99 01:47:31
My Email:skisue@aol.com

Comments:
I am Tanner's Great Aunt. I love you, Tanner.

wendy stainbrook - 05/24/99 01:41:54

Comments:
this page is dedicated to my son Tanner... I love you very much



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