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Conditions and Diseases > Muscular and Nerve Disorders Forum > Dystonia and other movement disorders
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Q: Dystonia and other movement disorders
asked by: distoweb on January 12th, 2009
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Hi friends of this great forum.

I come from Spain to this support group to collaborate after having done the same (I could say ‘successfully’) in similar groups in many countries along the world for a year.

I must say I started to live with torsion generalized dystonia (a movement rare disorder related to DYT1 gene mutation (torsin gene) that causes pain, cramps, lack of skill, etc., and many difficulties in daily life) when I was about 11. Now I am 43 and some months ago I felt I could help other people with my personal experience, my way of facing this illness now and in the past, and so on.
So here I am trying to share the keys of my experience, what I call ‘a positive approach to dystonia’ but also to… any other chronic, incurable, or similar disorder.

I use to say that, of course, I am not a model of anything, and I also say I trust those people who help you with an extra bit of understading, something so really expensive to get these days. ‘Understanding’: in my opinion, the best medicine to deal with.

In a simple way, and absolutely far from any interest but showing my own experience, I have spent long time months designing and developing a webspace from which I try to help sharing very carefully the best of me in a practical way and considerating not only physical aspects but animics too. You can also access to free pro physiotherapy advice.


Please, this is as yours as mine. Do not doubt doing with it whatever you feel it can be useful to other people, specially to ill people close to depression. I feel it can help.

My best wishes,

Fernando
Valencia-Spain
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