TMJ 'dysfunction' - Health implications

Within this forum, you will discover valuable insights on how a 'dysfunctional' jaw, dental arch anomalies, and various body asymmetries can contribute to illness from a unique perspective. This is your go-to resource for finding effective solutions and achieving lasting relief.
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 Post subject: Diagnosis of "my"MS...
PostPosted: Sat, 13 Oct 2012, 9:55 pm 
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Joined: Wed, 03 Oct 2012, 8:58 am
Posts: 14
My initial symptoms were my right hand weakness & feeling tired, this was put down to carpal tunnel syndrome and just generally being run down, after a series of tests CT was eliminated so I was then referred to a neurologist.

I had two MRI's and clinical tests and was informed by my neurologist ( Dr Woolmore) that I had aggressive RRMS although he said I was a difficult case to read and was recommended a steroid infusion, the steroids made me feel terrible, I was then told I was fortunate that Tysabri funding had been agreed and it's the best drug out there for me.
From day one the Tysabri made me feel very poor but i was encouraged to persevere. Over the next 12 months I showed no signs of remission and continued to worsen although my neuro seems to think I haven't progressed much!

I then had a precautionary blood test for PML. The result is that I am now JCV positive.

I then had a lumber puncture which turned out to be clear!

I have been drug free for 10 weeks now and have lost all faith in my MS team. :evil:


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