MS Hug questions
I continue to experience something that I think is the MS hug. I have asked my doctor about it and she says it is probably not because I don’t have a new lesion. However I realize that the pain has existed since my last lesion- I just thought I was having kidney pain. It was bad enough for me to go to the er at least twice and they always said it was not my kidneys… but they would give me antibiotics for a potential uti anyway. And then it would go away. Now I am experiencing it more frequently - it happens when I am really tired.. and it wraps around the left side of my chest.

It sounds like ms hugs. I had them more frequently when o was fist diagnosed (for a few years) and then they went away and recently come back. Totally random and unable to correlate to an action I was doing.
The hugs are real. They do exist and my neurologist told me from my initial diagnosis. Real!!