SLA is slowly taking life. Save!

The first symptoms of the disease did not worry me. I did not allow myself to think that something might be wrong. I did not think that the disease could be so dangerous that it could make my day take its toll ... For three years I had been struggling with health problems, which initially manifested themselves through weight loss and problems with movement. Finally, the moment came when I found myself in the hospital for research that seemed to be endless. After a few weeks, I heard what seemed to be the worst possible diagnosis - amyotrophic lateral sclerosis ...

I lost hope that one day I would regain my former fitness. I move on crutches, but my muscles are in worse and worse condition, soon my legs will be replaced by a wheelchair, I will be able to breathe only thanks to a respirator. The costs that I have to face due to my illness are enormous, insurmountable for me. Rehabilitation alone is not enough. I should take medications, have professional medical equipment to make my life with the disease as easy as possible. Please help me!