New to this site.

I have just joined your HSP site. I was diagnosed in 2003, with 99% probably HSP. I had full tests done at the Royal Free hospital in London. I spent 9days in there, being thoroughly looked at by professional and student Neurologists. I am convinced that I do, indeed have HSP. I do not know the PESKY gene responsible as it has not been identified as yet.....
I am the only member of my family with HSP as far as I know. I find it a quite common thing with other member's of the UK and USA HSP sites. My walking has deteriorated quite a bit in the past year. This may be the result of selling/moving home and all that it entails. We are getting settled now and will resume doing physio everyday, as I find this helps with my balance and helps keep my muscles supple as can be. I own two wheelchairs. A scooter. (Which I prefer). I use crutches/walking sticks and afo's with arch supports to help with the little amount of walking that I do.
Thank you for reading. :
I love your emoticons.
Dels.
I am the only member of my family with HSP as far as I know. I find it a quite common thing with other member's of the UK and USA HSP sites. My walking has deteriorated quite a bit in the past year. This may be the result of selling/moving home and all that it entails. We are getting settled now and will resume doing physio everyday, as I find this helps with my balance and helps keep my muscles supple as can be. I own two wheelchairs. A scooter. (Which I prefer). I use crutches/walking sticks and afo's with arch supports to help with the little amount of walking that I do.
Thank you for reading. :

Dels.