Hi, I’ve only tried replying a couple of times, so I hope this works. When I read your post I felt like I was reading my life story. I have been diagnosed and undiagnosed with ms so many times since college and am in my 60’s. Fatigue, brain fog, pins and needles the whole bit. Not making a diagnosis, but do some research into mast cell activation syndrome. I have many autoimmune diseases that were driving me crazy trying to get a dr to listen until this June when bingo I was diagnosed with mcas. Hope this helps. Just realized posted to wrong place so @czechmate I hope you get this. John knows how technologically challenged I’m