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Still No Answers..Is it Just Me?

Autoimmune Diseases | Last Active: Sep 8, 2025 | Replies (24)

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Profile picture for krisingle1 @krisingle1

I sort of feel like I'm in the same boat. I'm in the process of testing - looking into rhuematoid arthritis and it's most likely? EDS but I can't get in to see the MDs for months and months to actually run the tests and do the evaluations so for now I'm just in PT. Some days are okay but others are awful and sometimes I wake up from it in the middle of the night feeling like one of my joints is exploding like a dying star. No one in my family seems to have much sympathy - including some of my internists and I'm getting frustrated. I'm not generally whiny about pain so I think this is probably pretty bad. I also seem to have a chronic headache which may be related or may just be stress but I'm pretty upset about my family's (non) reaction. It's more complicated than just the health stuff but it sure sucks so I can empathize with your situation. Good luck with your diagnosis! I feel for you.

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Replies to "I sort of feel like I'm in the same boat. I'm in the process of testing..."

Thanks for your response. Hang in there, I know the pain is not fun and the lack of answers, waiting on doctors, etc... can truly be frustrating. If there is good news, it is that I am seeing from this forum that my situation is not unique and there are lots of others who are suffering and have no answers. Guess that gives me some solace in some strange way. Best to you and hopefully you can get some answers soon!!