SSR

What is the level of research?

Tuesday, May 15, 2007

Your Questions

I'm with multiple sclerosis since my 21 years (December 2001) ... OA ¹ Fort interregional in my search! Today the salaries are a real crosses, or an injection every day (with devastating effects on the skin and a painful) or an injection per week (with side effects of flu), etc ....

Do you know that we are about 85 000 young people in France? And that is the 1st cause of disability among young adults? It is still a big concern for society, since the number is growing increasingly every year! 50 000 in 2001 to 85 000 in 2007 !!!!!!!!!

But we never speaks to us, we do talk about us to show that people in wheelchairs, or severely dependent! So people are afraid of us! It was a bad image must be recognized!

So in reality, more than 3 / 4 of people living, working, living on virtually sociable (according to the place that it gives us of course!)! But the image we give of this disease is so dull that we must not say anything about our health! We hide, lie etc. .. What is not normal !!!!!

So my question is: Go promote research centers so that we will find the "remedies" against this disease? Will you support research that we have finally treatment with oral medication Will you develop campaigns to encourage donations to promote a better understanding of this disease so diverse in its symptoms??

Thank you kindly consider my message because it is a cry from the heart of several "sépiens" that addresses today!

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