Then, when things started getting quite difficult I couldn't get access to a neuro because none of my symptoms was particularly severe - no optic neuritis or sudden numbness or loss of movement - in our health system this equals go to the bottom of the waiting list as a very low priority and sit there forever. I had vague and gradually worsening symptoms for some years, and didn't really talk to my GP about them until they were starting to significantly interfere with daily life - I had previously just attributed them to getting older, heading into menopause, and not being particularly fit.
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She didn't think my GP was taking very good care of me. I finally got to switch to a woman doctor in the same clinic, she agreed to take me as a patient. I didn't have any nerve damage, I had so many lesions in my brain that it showed I had MS for quite a while. When the neuro looked at my history he said I will test for nerve damage but I am also testing you for MS. He said to me "They can't do any thing for you anyways". I said to him when I got the referral, maybe they will test me for MS.
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He finally gave me a neuro reference when he thought I had damage the nerves in my elbow throwing on my potters wheel. I have a extensive history of family members with MS and ALS and he knew that. I had symptoms for at least 10 years and even had MS hug problems for 3 months. This GP was our doctor because he had bought our retired doctors practice and had to take us. The company my husband worked for had a unusual health insurance and it was nearly impossible to get a GP. He thought I was a hypochondriac and would denied me every time.
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I begged my GP for at least 10 years to give me a reference to a neurologist for MS testing.