Hi there. I was diagnosed with Fibromyalgia 3 years ago but I feel my symptoms are worsening and suspect possible MS. I now walk with a stick due to balance issues and my muscle twitches are becoming more noticeable to others. Fatigue is also off the scale. If i mention symptoms to gp I’m made to feel that i am imagining everything. Feel so down about it all. I’m a shadow of my old self. Does anyone else feel or have felt the same?
Hi, change Gp if possible…course it’s not in your head.
Took 22 years to diagnose my PPMS.
Need lots of help now. got good team supporting me.
hard to type.
boudsx
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