My 24 year old son (was 23 at the time of diagnosis) was diagnosed with ALS in March 2021 and I have him on the list at Mayo. If anybody out there can offer any feedback on stem cell I would appreciate it. We had genetic testing done and nothing was found so his ALS is sporadic I guess. As far as that goes, any positive recommendations at all would be appreciated. My wife, my other son, and myself are all devastated that our youngest member of our family has been found to have this disease.
What is the NHS? Is that a European health institute? My 23 year old son was recently diagnosed with ALS and am looking for any help I can get for him.
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