I am 16 years old, 4'8 tall & Hemipelgia Cerebral Palsy. Sometimes my friends or cousin who are my 7-24 years old cousin or friends will help me out. I love you my friends & cousin alot.
hey Kim, wow Jasons youtube and website are doing good.Did you read my screenname?lol.I just love Jasons $11111,00000 smile.His smile brings more smiles into this world.Ive know Jason for three years[hole life] and he has changed so much.Before he was so stiff I couldent even undress or dress him, but now hes way more relaxed.Jason has come along way. I love you Jason, more than words can discribe, and more than the world it self!Angela.
Thank- you, people tend to for get about her because she has mild cp. They have to be 4 to do that. I found this excersise equipment at Brookstone called I-Gallope, Its like your really riding a horse so we but them on for 1 hr a day. And he Loves the Jacuzzi.I hope you sined my guestbook. Thanks-again Kim
it is difficult, and there will be challanges and difficulties, and sometimes he'll ask why and become angry. But, if you really look into his eyes, ht's happy. thats good. he'll go far. he looks determined.
all it takes is determination.
and faith.
and ok, so some really good parents and therapists don't hurt either!
I can see how bad he wants to do these things and it takes so much effort from him to even hold his head up but when he does he is so proud. Holding a sucker he enjoys every moment because that is the only thing he will /can hold for at least 30 min. I so love looking into those eyes of his that is how I learned there is No Limits for my son. I think the best thing that helped Jason was Hbot. It worked right away for him. Thank- you again for such sweet words. KIM
i was born in 90 so..I guess i'm one of the lucky ones.spastic diplegia with that oh so lovely strabismus. my treatments were therapy, surgey, and botox.
it's deff. not fun, but its there for a reason! just remeber that when he hits his teens! I dont know if you are religious or not, but this helped when I felt hopless and hated myself. Who knows, it might come in handy
"Oh God, help me to believe the truth about myself, no matter how beautiful it is."
You sound like a fighter and a awesome kid. Taking the time to share with me alone tells me you are a good person. Your parents must be very proud. HBOT is short for hyperberic oxgen treatments. It is amazing. You breath 100% oxygen and what it does is wake up sleeping brain cells we all have them.
It teaches your brain to take other pathsways to do things. Jason was stiff as a board Know he is so loose, he can kick and reach out. For the first year in a half he could not sleep know matter what the dr's put him on, his brain did not know sleep. Now he sleeps 10 hours and naps. His body jerked all day and all night after 5 hours out of 40 no more spatisity. a He could not have a bowel movement because that is muscle the next day no problems there.
Jason was blind for the first year, after is hbot he started tracking now he can see two feet out, maybe more. you can google it or look on Jason web for more info- there is a picture of him getting his hbot.Thank you for sharing and I do beleive in God ,I will remember what you have said. God Bless kim
that is so amazing! The technology they have now just amazes me. If you have seen such improvent these past few years, imagine what the future holds!!! Anyway, Jason is an adorable boy!
ok so last comment. I was reading on your website about your daughter. thought about how lucky she was to be diagnosed at an early age! anyway, here's a suggestion that tends to be underlooked. I believe they now call it Hippotherapy, but when i did it, it was just theraputic ridinng lessons. It helps with balance and muscle tightness quite a bit. Hydrotherapy, or just therapy in a warm pool, works really well too!
Amazing video, AMAZING LITTLE BOY!!!! With Jasons will and the loving support of Kim and John there truly are NO LIMITS for Jason. He will achieve everything he sets out to. I feel so very blessed to be his Aunt! I love you Jason!!!!
I love you so much Jason. I am so proud of all that you do. Your 80 crunches a day,and amazing willingness to hold your head up no matter how hard it is, show us that there are No Limits for you. I am so blessed.. Mommy loves you.
Your Son is amazing! I have CP, not at the level of your Son but I hope maybe my experience may help ease your thoughts on the upcoming years of your Child
Thank-you. You sound preety amazing yourself. Any advice is welcome. It's so much better getting advice from someone who can share first hand what he(Jason)might be feeling.
Beautiful Video For Your Son! He's Such A Smiley Little Guy!, Just Like Our Kylie! It Warms My Heart To Know Another Child Is Out There Fighting The Same Battle And Winning Against The Odds! God Bless.
Thank-you very much.. I always say he has a Million Dollar Smile. They have won the Battle now they are recovering and there are No Limits for our babies. God Bless KiM
I am 16 years old, 4'8 tall & Hemipelgia Cerebral Palsy. Sometimes my friends or cousin who are my 7-24 years old cousin or friends will help me out. I love you my friends & cousin alot.
Love Michaela
birds16ful 2 years ago
WOW! RESPECT IS ALL I HAVE!
AbiliTV - Where it's about the ABILITY... Not "dis" part.
SpinergyDude 3 years ago
Jason, you are special little boy, who will achieve these things that have come your way. Always remember how much you are loved.
haveseven 4 years ago
hey Kim, wow Jasons youtube and website are doing good.Did you read my screenname?lol.I just love Jasons $11111,00000 smile.His smile brings more smiles into this world.Ive know Jason for three years[hole life] and he has changed so much.Before he was so stiff I couldent even undress or dress him, but now hes way more relaxed.Jason has come along way. I love you Jason, more than words can discribe, and more than the world it self!Angela.
iluvjason3 4 years ago 3
Thank- you, people tend to for get about her because she has mild cp. They have to be 4 to do that. I found this excersise equipment at Brookstone called I-Gallope, Its like your really riding a horse so we but them on for 1 hr a day. And he Loves the Jacuzzi.I hope you sined my guestbook. Thanks-again Kim
jGRHUEAHGIR 4 years ago 2
Your son has an amazing future in store.
I can see it in his eyes!
moravianfaith 4 years ago 5
THANK-YOU,Thanks for such sweet and promising words. God Bless Kim
jGRHUEAHGIR 4 years ago 3
i should know!
i have CP too. not as bad as Jason.
it is difficult, and there will be challanges and difficulties, and sometimes he'll ask why and become angry. But, if you really look into his eyes, ht's happy. thats good. he'll go far. he looks determined.
all it takes is determination.
and faith.
and ok, so some really good parents and therapists don't hurt either!
moravianfaith 4 years ago 4
I can see how bad he wants to do these things and it takes so much effort from him to even hold his head up but when he does he is so proud. Holding a sucker he enjoys every moment because that is the only thing he will /can hold for at least 30 min. I so love looking into those eyes of his that is how I learned there is No Limits for my son. I think the best thing that helped Jason was Hbot. It worked right away for him. Thank- you again for such sweet words. KIM
jGRHUEAHGIR 4 years ago 3
he will amaze you! the Hbot?
i was born in 90 so..I guess i'm one of the lucky ones.spastic diplegia with that oh so lovely strabismus. my treatments were therapy, surgey, and botox.
it's deff. not fun, but its there for a reason! just remeber that when he hits his teens! I dont know if you are religious or not, but this helped when I felt hopless and hated myself. Who knows, it might come in handy
"Oh God, help me to believe the truth about myself, no matter how beautiful it is."
moravianfaith 4 years ago 3
You sound like a fighter and a awesome kid. Taking the time to share with me alone tells me you are a good person. Your parents must be very proud. HBOT is short for hyperberic oxgen treatments. It is amazing. You breath 100% oxygen and what it does is wake up sleeping brain cells we all have them.
jGRHUEAHGIR 4 years ago 2
It teaches your brain to take other pathsways to do things. Jason was stiff as a board Know he is so loose, he can kick and reach out. For the first year in a half he could not sleep know matter what the dr's put him on, his brain did not know sleep. Now he sleeps 10 hours and naps. His body jerked all day and all night after 5 hours out of 40 no more spatisity. a He could not have a bowel movement because that is muscle the next day no problems there.
jGRHUEAHGIR 4 years ago 2
Jason was blind for the first year, after is hbot he started tracking now he can see two feet out, maybe more. you can google it or look on Jason web for more info- there is a picture of him getting his hbot.Thank you for sharing and I do beleive in God ,I will remember what you have said. God Bless kim
jGRHUEAHGIR 4 years ago 2
wow.
that is so amazing! The technology they have now just amazes me. If you have seen such improvent these past few years, imagine what the future holds!!! Anyway, Jason is an adorable boy!
best wishes!
moravianfaith 4 years ago 3
Thank-You and Best of luck to you. Kim
jGRHUEAHGIR 4 years ago 2
ok so last comment. I was reading on your website about your daughter. thought about how lucky she was to be diagnosed at an early age! anyway, here's a suggestion that tends to be underlooked. I believe they now call it Hippotherapy, but when i did it, it was just theraputic ridinng lessons. It helps with balance and muscle tightness quite a bit. Hydrotherapy, or just therapy in a warm pool, works really well too!
moravianfaith 4 years ago 3
Amazing video, AMAZING LITTLE BOY!!!! With Jasons will and the loving support of Kim and John there truly are NO LIMITS for Jason. He will achieve everything he sets out to. I feel so very blessed to be his Aunt! I love you Jason!!!!
Aunt Marybeth
JLCJK 4 years ago 4
He feels Pretty blessed to have such a wonderful Aunt in his life..Thank-You for the suport. Kim
jGRHUEAHGIR 4 years ago 3
I love you so much Jason. I am so proud of all that you do. Your 80 crunches a day,and amazing willingness to hold your head up no matter how hard it is, show us that there are No Limits for you. I am so blessed.. Mommy loves you.
jGRHUEAHGIR 4 years ago 3
Your Son is amazing! I have CP, not at the level of your Son but I hope maybe my experience may help ease your thoughts on the upcoming years of your Child
AJBR1980 4 years ago 3
Thank-you. You sound preety amazing yourself. Any advice is welcome. It's so much better getting advice from someone who can share first hand what he(Jason)might be feeling.
jGRHUEAHGIR 4 years ago 2
Beautiful Video For Your Son! He's Such A Smiley Little Guy!, Just Like Our Kylie! It Warms My Heart To Know Another Child Is Out There Fighting The Same Battle And Winning Against The Odds! God Bless.
Audrey AKA: Country By Audrey
CountrybyAudrey 4 years ago 2
Thank-you very much.. I always say he has a Million Dollar Smile. They have won the Battle now they are recovering and there are No Limits for our babies. God Bless KiM
jGRHUEAHGIR 4 years ago 3