
Multiple Sclerosis (MS) Support Group
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Does anyone have chest pain attributed to MS?

deleted_user
I have chest pain, which I won't describe. I have had this for the last 20 years. Numerous stress tests, angiogram, and endoscopes, and no culprit.
My question for you, do you have chest pain, attributed to MS, and describe what it is like.
Thanks. Looking for answers.
My question for you, do you have chest pain, attributed to MS, and describe what it is like.
Thanks. Looking for answers.
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My thoughts on the right side pain, usually gall bladder. Gave mine up 10 years ago.
I was hoping someone might describe what I feel, as no doctor believes what I feel, as no test verifies anything for them.
I have a pressure that builds up in the center of my chest, (when Alien the movie came out, I called it my little Alien) usually with a certain period of exertion. This year I also get pulses of pain that start in the same place as the pressure and its seems to be pulsing upward toward my neck.
When I get the pressure sometimes, I find the best position for me to go to the floor, until it stops, which usually isn't too long.
Now I get the pressure walking across the street, up a hill. It got extremely worse after I picked up a 24 bug from Grandkids back in March of this year. It has gotten better, but not back to where it was. Since that time I have been to Cardio and Gastro Docs and nothing.
Gastro Doc put me on a low dose of Amitriptyline and it seems to help a little, but not enough.
It hurts in the front, like someone sitting on my chest, but it hurts in my back ribs and backbone as well. Feels like the bones need popping or something. It's definitely all around me. It doesn't go below the ribs. Sound familiar?