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Hi guys,
For years I have suffered from fatigue, bad breath, body odor, easily crying, muscle weakness and various other problems. More importantly I also have wide hips (TOO wide clearly wide). My other problem is I have neurological issues...I don't think the same way other people do at least I feel so. I'm quieter then others and oh yeah I have SEVERE anxiety which affects my day to day life. At first I didn't want to believe it was genetic because that would mean my life was over. If I have to battle this condition for the rest of my life then I have nothing left at all but I have a feeling it is genetic.
Anyway my question is simple...
My doctors won't take me seriously at all. If I have A RARE genetic condition which may only affect a small group of people in the world how would I get diagnosed??? Is there a way to get diagnosed on the NHS or can I go somewhere to get diagnosed???
Thank you for replies and sorry if this isn't CFS related I wasn't sure who to ask.
For years I have suffered from fatigue, bad breath, body odor, easily crying, muscle weakness and various other problems. More importantly I also have wide hips (TOO wide clearly wide). My other problem is I have neurological issues...I don't think the same way other people do at least I feel so. I'm quieter then others and oh yeah I have SEVERE anxiety which affects my day to day life. At first I didn't want to believe it was genetic because that would mean my life was over. If I have to battle this condition for the rest of my life then I have nothing left at all but I have a feeling it is genetic.
Anyway my question is simple...
My doctors won't take me seriously at all. If I have A RARE genetic condition which may only affect a small group of people in the world how would I get diagnosed??? Is there a way to get diagnosed on the NHS or can I go somewhere to get diagnosed???
Thank you for replies and sorry if this isn't CFS related I wasn't sure who to ask.