Recent content by Froggyhop

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    How common is eye pain and blurry vision in fibromyalgia? What are your experiences?

    Hi Uhura, I have not been officially diagnosed with FM, still ticking off all the other medical boxes that are required before the docs will seriously look at FM. I have eye issues also, and am not receiving any answers from the eye doc who I just saw again 2 weeks ago. He too tells me that the...
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    Reaction to Small Fiber Neuropathy Skin Biopsy

    Hi JayCS! Thank you for responding to my post! There is a website www.healthrising.org that has great, current research information on FM, ME/CFS, and Long Covid, which have interesting connections between them, including SFN. Boston is a kind of hot spot for this research, if you look up Dr...
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    Reaction to Small Fiber Neuropathy Skin Biopsy

    Hi, I am not officially diagnosed with FM at this time, I have spent the last 19 months seeing different specialists and checking off boxes. It has been an interesting and also challenging process. Two days ago I had a small fiber neuropathy skin biopsy, and I am having a rather intense reaction...
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    Newly diagnosed and feeling lost

    Hi Sunkacola and FM community! I am over the moon happy to have found this community of support. Grateful. Sunkacola, your post re self-empowered approach to dealing with FM is especially heartening and refreshing. I have yet to be officially diagnosed with FM, currently approaching the finish...
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