Comments on: Nathan Baker is proof positive that kids with disabilities can compete in sports. http://www.cpirf.org/stories/1228 Cerebral Palsy International Research Foundation Thu, 02 Feb 2012 12:40:20 +0000 hourly 1 http://wordpress.org/?v=3.2.1 By: sure did http://www.cpirf.org/stories/1228/comment-page-1#comment-2529 sure did Mon, 05 Dec 2011 23:46:13 +0000 http://cpirf.picrow.com/?p=1228#comment-2529 I thoroughly agree with your take on this matter. Thanks so much for sharing them with all of us. Are there any other articles like this one? I thoroughly agree with your take on this matter. Thanks so much for sharing them with all of us. Are there any other articles like this one?

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]]> By: DMV NC http://www.cpirf.org/stories/1228/comment-page-1#comment-1513 DMV NC Mon, 08 Nov 2010 16:24:55 +0000 http://cpirf.picrow.com/?p=1228#comment-1513 Teriffic post. Thanks Teriffic post. Thanks

]]> By: Houston Car Insurane http://www.cpirf.org/stories/1228/comment-page-1#comment-1259 Houston Car Insurane Mon, 11 Oct 2010 00:47:57 +0000 http://cpirf.picrow.com/?p=1228#comment-1259 Wonderful Website! I wanted to ask if I might be able to quote a portion of your site and use a couple of points for a term paper. Please drop me an email whether its ok or not. Thanks Wonderful Website! I wanted to ask if I might be able to quote a portion of your site and use a couple of points for a term paper. Please drop me an email whether its ok or not. Thanks

]]> By: mouth guard for grinding teeth http://www.cpirf.org/stories/1228/comment-page-1#comment-1112 mouth guard for grinding teeth Sat, 11 Sep 2010 09:56:18 +0000 http://cpirf.picrow.com/?p=1228#comment-1112 Wow! What a very cool blog! I am grateful to read this post; very inspiring story. This must be a great help to those kids like Nathan. To all supporters and stakeholders, you are really great I owe you for this very promising commitment you had. Very Nice blog! Wow!
What a very cool blog!
I am grateful to read this post; very inspiring story. This must be a great help to those kids like Nathan. To all supporters and stakeholders, you are really great I owe you for this very promising commitment you had.
Very Nice blog!

]]> By: June Stubbs http://www.cpirf.org/stories/1228/comment-page-1#comment-498 June Stubbs Thu, 29 Apr 2010 05:37:27 +0000 http://cpirf.picrow.com/?p=1228#comment-498 I don't know if you have considered hyperbaric therapy. We have a grandson, 9 years old who we put in the chamber, and have seen continued improvements. It is expensive, and I am considering purchasing a chamber, as we need it long term. The theory is that the brain tissue once thought to be dead, is actually dormat. The oxygen wakes up those areas, and actually grows new stem cells safely. Change takes time, but I am encouraged. You might also see if vital stem would be an option for helping Thomas swallow. Our child was on a feeding tube, and after 1 month of vital stem therapy, he could eat real food. A lot of doctors have never heard of this procedure, but it is non-invasive, and a shame that all medical doctors don't know about it. Best of luck to your family. I don’t know if you have considered hyperbaric therapy. We have a grandson, 9 years old who we put in the chamber, and have seen continued improvements. It is expensive, and I am considering purchasing a chamber, as we need it long term. The theory is that the brain tissue once thought to be dead, is actually dormat. The oxygen wakes up those areas, and actually grows new stem cells safely. Change takes time, but I am encouraged. You might also see if vital stem would be an option for helping Thomas swallow. Our child was on a feeding tube, and after 1 month of vital stem therapy, he could eat real food. A lot of doctors have never heard of this procedure, but it is non-invasive, and a shame that all medical doctors don’t know about it. Best of luck to your family.

]]> By: Shawn Cantrell http://www.cpirf.org/stories/1228/comment-page-1#comment-125 Shawn Cantrell Tue, 27 Oct 2009 19:32:27 +0000 http://cpirf.picrow.com/?p=1228#comment-125 My son is now 7 years old. We live in rural Kansas and are 2 hours to all the resources I can find on getting help for my son. We travel to Kansas City 2 1/2 hours to go to Children's Hospital. I am trying to come up with new resources as well as latest ideas of therapy as most of help he gets is from myself since we live in such a rural area. IF ANYONE READS THIS AND HAS ANY IDEAS ON WEBSITES OR OTHER RESOURCES THAT I CAN UTILIZE TO COME UP WITH THERAPIES PLEASE EMAIL ME AT worldiver@gmail.com My son and I would be forever indebted to you. We moved 30 miles to another small town that has a physical therapist who comes twice a week to the school so he is getting some help that way. This therapist will not accept health insurance so we have to pay out of pocket for any additional help. I wish I could find someone who takes health insurance. I have also taken him to Kansas City for multiple BOTOX injections and have casted his foot which both seemed to help somewhat. I am looking for therapies for right hand and foot as well as saliva (swallowing). My son suffered an infarction which affected 1/2 of the left side of his brain. I could not be more proud of the progress he has made. I was told at his diagnoses that he may never crawl, walk or talk. By the grace of god and Thomas' persistence he is getting good grades in 2nd grade and can throw and kick the football unbelievably far. IF ANYOINE HAS IDEAS ON THERAPIES FOR RIGHT HAND AND ARM PLEASE SEND ME WHATEVER YOU CAN THINK OF. PLEASE. God Bless, Shawn Cantrell Father of Thomas Cantrell email worldiver@gmail.com 933 Madison Street Fredonia, KS 66736 620-625-3030 My son is now 7 years old. We live in rural Kansas and are 2 hours to all the resources I can find on getting help for my son. We travel to Kansas City 2 1/2 hours to go to Children’s Hospital. I am trying to come up with new resources as well as latest ideas of therapy as most of help he gets is from myself since we live in such a rural area. IF ANYONE READS THIS AND HAS ANY IDEAS ON WEBSITES OR OTHER RESOURCES THAT I CAN UTILIZE TO COME UP WITH THERAPIES PLEASE EMAIL ME AT worldiver@gmail.com My son and I would be forever indebted to you. We moved 30 miles to another small town that has a physical therapist who comes twice a week to the school so he is getting some help that way. This therapist will not accept health insurance so we have to pay out of pocket for any additional help. I wish I could find someone who takes health insurance. I have also taken him to Kansas City for multiple BOTOX injections and have casted his foot which both seemed to help somewhat. I am looking for therapies for right hand and foot as well as saliva (swallowing). My son suffered an infarction which affected 1/2 of the left side of his brain. I could not be more proud of the progress he has made. I was told at his diagnoses that he may never crawl, walk or talk. By the grace of god and Thomas’ persistence he is getting good grades in 2nd grade and can throw and kick the football unbelievably far. IF ANYOINE HAS IDEAS ON THERAPIES FOR RIGHT HAND AND ARM PLEASE SEND ME WHATEVER YOU CAN THINK OF. PLEASE.

God Bless,
Shawn Cantrell
Father of Thomas Cantrell
email worldiver@gmail.com
933 Madison Street
Fredonia, KS 66736
620-625-3030

]]> By: debbie walls http://www.cpirf.org/stories/1228/comment-page-1#comment-48 debbie walls Mon, 21 Sep 2009 03:04:37 +0000 http://cpirf.picrow.com/?p=1228#comment-48 my grandson was born at 26 weeks and had a grade 4 bleed causing rt hemaparasis we have fought many battles for him he has rt sides weakness of leg and hand received PT OT at our local children's rehab at $40 copay every week which is a finacal burden since we have insuranse and can't get any outside help we go with out food to take care of him but he is worth every hungry moment and he never goes hungry.It looks like you have success stories and its nice to see you always hear the bad never good Jaccob wasnt dx till he was 4 1/2 yr old which was a major shock your agency seems to care and that feels my heart and to know someday with our help and all the therapy we do at home he someday play a sport when they advised us to put in group home or institution when he was born so proud and admire the job you do my grandson was born at 26 weeks and had a grade 4 bleed causing rt hemaparasis we have fought many battles for him he has rt sides weakness of leg and hand received PT OT at our local children’s rehab at $40 copay every week which is a finacal burden since we have insuranse and can’t get any outside help we go with out food to take care of him but he is worth every hungry moment and he never goes hungry.It looks like you have success stories and its nice to see you
always hear the bad never good Jaccob wasnt dx till he was 4 1/2 yr old which was a major shock your agency seems to care and that feels my heart and to know someday with our help and all the therapy we do at home he someday play a sport when they advised us to put in group home or institution when he was born so proud and admire the job you do

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