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,

Hi, my daughter is also 4 l/2 and she is/was getting hippotherapy, my

insurance company was paying for it, since March of last year, and no they

will not. They are now paying for P.T. at home (she gets some at school thru

the school distrcit), anyway she is not yet walking but taking steps, her

balance and gait are still off so we picked up therapy at home after school,

she also had to have hip muscle releases cuz she was so tight, anyway since

we got P.T. at home they are telling us it is a duplication of services so

they wont pay for hippotherapy anymore. It is $60 for l/2 hr session. She

LOVES it and I know she has improved its just that this is another expense.

I appealed there decision and was denied so now I am appealing at an outside

level. DOes anyone have any further info that might help us to convence the

right people it works.

Cathie, mom to 4l/2 CHARgER

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Cathie, Tim also gets pt at home as well as school, they have decided that

they will pay for 30 sessions of pt per year--he gets it 1x a week--so looks

like we will be appealing that too. Our pt is also a friend , so we may be

able to work out a payment plan or something-we'll see. Someone suggested

contacting the commision of the blind to see if they could help? Don't know

if you are involved with anything like that? it's definitely a problem--it

can be taken off taxes at the end of the year, but that's not much of a help

either. Hopefully, we'll get some help --hope gets better and walks

soon. Tim is still not the best walker balance -wise but he gets where he

wants to go. maria

Re: hippotherapy

> From: NPTQueenie@...

>

> ,

> Hi, my daughter is also 4 l/2 and she is/was getting hippotherapy,

my

> insurance company was paying for it, since March of last year, and no they

> will not. They are now paying for P.T. at home (she gets some at school

thru

> the school distrcit), anyway she is not yet walking but taking steps, her

> balance and gait are still off so we picked up therapy at home after

school,

> she also had to have hip muscle releases cuz she was so tight, anyway

since

> we got P.T. at home they are telling us it is a duplication of services so

> they wont pay for hippotherapy anymore. It is $60 for l/2 hr session.

She

> LOVES it and I know she has improved its just that this is another

expense.

> I appealed there decision and was denied so now I am appealing at an

outside

> level. DOes anyone have any further info that might help us to convence

the

> right people it works.

> Cathie, mom to 4l/2 CHARgER

>

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> For information about the CHARGE Syndrome

> Foundation or to become a member please

> contact marion@... or visit

> the CHARGE Syndrome Foundation web page

> at http://www.chargesyndrome.org

>

>

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On Saturday, we awarded a scholarship to pay for hippotherapy to a deafblind girl in Kansas. So, I am so excited to hear all of the positive things you are saying about it!

Shari Willis

of Katlyn's Hope

hippotherapy

Hi, my son Timmy 41/2, has been involved with two different hippotherapy sessions. We have found it to be very helpful for him. He has very poor balance, but we started hippotherapy last fall and within a few weeks he was walking independantly. He was on the verge for about 9 months and just coudn't get over the hump. He is very fearful of large things, but got right on the first day and did great. At the first facility it was strictly pt in different positons on the horse. At the new facility(because the old one was strictly outside and quit for winter), it is a riding stable and they are teaching him the basices of riding also--English--which I feel is better for him. He is still getting the pt, but he's also learning to ride.

The price is also different--the first place was $50 dollars for a half hour--which our insuarnce covered 80%--but our insurance has changed so we don't know yet what if any they will pay. The second program is through the rec dept. of another county so it runs $240 for 10 weeks. More because it's out of county --a 45 minute drive, but I feel it's worth it--and like I said I don't know how much ins. will pay. Our Dr. is very goood about writing scripts for therapy though.

You can call NARHA at 1-800-369-ride and get info for your areas they also have a web-site.

best of luck I hope it helps, I have know many people gettin involved that it has helped.

, mom to Timmy4 charger, Keegan 2 on 3/20 and wife to pat

For information about the CHARGE Syndrome Foundation or to become a member please contact marion@... or visit the CHARGE Syndrome Foundation web page at http://www.chargesyndrome.org

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,

<< I don't know how much ins. will pay. Our Dr. is very goood about writing

scripts for therapy though.

>>

My son Tim rode for 5 years and we had our local Elks Club sponsor him. They

covered the total cost (which as I recall was about $100/mo) and the required

insurance. We never had to reapply and we never saw a bill for the entire 5

years.

Tim really benefitted from the experience and we looked at it as being his

sport -as all the neighborhood kids were out playing baseball and soccer

which he did not have the physical capability to do at that time.

Also, sure saves the hassle of having the insurance company involved in yet

another

part of our lives.

Donna

mom to Tim (14), (13), (10) and (5 1/2)

Hamilton Sq. NJ

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Hi!

has had dramatic results with hippotherapy including: improved balance,

tone, posture, walking, and resolution of his scoliosis! His pediatric

orthopedic surgeon wrote: " Review of his x-rays today demonstrate no measurable

thoracic or lumbar scoliotic curves, and his thoracic kyphosis is well in the

normal range. This is significantly changed from his previous visits. Our

impression is that is doing quite well at this time. He seems to have

had a significant improvement since he has begun walking and also with his

horseback riding therapy, as this provides additional trunk strength and control

Our recommendations are: ......2. We would advise that he continue with

horseback therapy. We feel that this has improved his tone considerably, and

his upper body control and strength is significantly improved. " This was the

first report following starting hippotherapy and was the only thing that had

changed. On Monday he was evaluated again. I showed 's school pictures

before and after hippotherapy. He said, " AMAZING! Visually he still looks

straight even though he has had very good growth with his growth hormone

therapy. Continue with the hippotherapy! " A picture is worth a thousand words

and the difference is truly amazing-he went from looking like a spineless kid to

an athlete. : ) Perhaps because we have documentation of the benefits, were

able to get it written into his ESY services for last summer, and the new

district (we switched programs this year and have been VERY HAPPY with the

results and services) has the hippotherapy program at one of it's facilities;

his new school is paying for hippotherapy once per week year round. : ) Maybe

also because we help raise lots of $ for their annual fundraiser to support the

hippotherapy program and the director recently said could be a poster

child for hippotherapy. Hmmm.... yes he could!

Cheryl, , (6), (4, CHaRGE)

MI

>>> oganm@... 03/14/00 01:35AM >>>

I've had a request about information/benefits of hippotherapy. Anyone with

experiences, please forward those to me so I can pass that along to this

individual.

Thanks,

Marilyn

oganm@...

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For information about the CHARGE Syndrome

Foundation or to become a member please

contact marion@... or visit

the CHARGE Syndrome Foundation web page

at http://www.chargesyndrome.org

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