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Re: Strollers?

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Hi Tamara:

I know can walk at times, but if you are looking for easy walking over

uneven surfaces, etc. for pushing we got a kidkart for our daughter. But if

you go to a medical supply place they will be able to guide you in the

direction you need to go and actually have several pieces of equipment for

you to see and try in. At least our place does. Leah can't walk, but

has good support, but we chose the kidkart because it has larger wheels to go

on blacktop and even the grass fairly easy compared to a stroller, and it's

back can recline, but what else I like about it is the height. It is a

little higher than a wheelchair so if we would go to the zoo or such, she can

see better and it goes right up to table height. It doesn't allow the arms

to go under the table; but it includes a tray that we use when we go out and

she can't be close to the table to eat. Also if you go to FlagHouse.com you

will be able to see strollers there. I love our kidkart now and am so glad

to have gotten it. At first I didn't want that " wheelchair " look, but my two

boys can push Leah in it easily, too. Of course she is only may be 31 lbs.

if that. Good luck.

Nerenhausen

mom to Leah

fairgrovejoe wrote:

> Does anyone know who makes a stroller that will hold larger than 40

> pounds? gets so tired everywhere we go and he is getting too

> large for the shopping carts. Yet I do not feel he is ready for a

> wheel chair. He does fine at home! And fine for short distances!

> Any ideas would be great!

> Tamara(mommy of age 4, unspecific mito)

>

> Please contact mito-owner with any problems or questions.

>

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try checking out this link for some options

http://www.adaptivemall.com

you have to do searches online under pediatric wheelchairs, but then you will find stroller type chairs, buggies, etc.. as well :)

we just got a convaid crusaire for my son . His dad thinks it's wonderful. for me the jury is still out...i'm having a hard time with pushing it but I think it's because of my fybromyalgia....

good luck!

ps. if your insurance won't pay for one..or you can't afford one yourself...we were able to get 's payed for through the muscular dystrophy association

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