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Hi everybody !

Thank you for approving my request to join the group.

I'm 23 and have type 2 SMA. I've been living near Paris since my birth.

& I tend to go to the US for an exchange programm with my school.

That's why I need your help to have further information about :

-The accessibility in the US : would it be better for me to go in a big City

such as Boston, Chicago or would it be possible to go in a smaller one ?

Is each public transport accessible to an electric weelchair ? Are all the

schools accessible ?

- Medical : Where could I rent medical materials, such as medical bed... Do

you have some good adresses ?

- Is there among the SMA community some students who could give me some

advices and speak about their experience ?

Thanks a lot for your help

Look forward to hearing from you

tte

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