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Old 10-02-2016, 11:46 AM
DavidHC DavidHC is offline
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Join Date: Nov 2015
Posts: 732
8 yr Member
DavidHC DavidHC is offline
Member
 
Join Date: Nov 2015
Posts: 732
8 yr Member
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Thanks for your note and concern. But I've never had the ESR test. I have been negative for ANA and all other markers. It's not impossible that I have Sjogren's but I don't think the most likely. All testing was negative, my symptoms could just as well be from SFN and I'm male. I'm not sure I want to have a lip biopsy at this point with all this standing against the possibility, but I do plan to eventually see another rheumatologist. It's just that the one I saw was the leading specialist in Canada, but that may not mean much, since he seemed pretty set in his ways in some respects.


Quote:
Originally Posted by MAT52 View Post
DavidHC I remember following your posts a while ago and I'm sure you had a very elevated ESR? I wanted to tell you that this could be a very good indicator of Sjogren's if I'm right in what I've remembered. People with SS often have high inflammatory markers because of the systemic dehydration which causes blood to be thicker and higher in protein.

I also should say that I was only officially rediagnosed by a new rheum in a new hospital about five weeks ago. This was because he saw my high PV/ ESR and raised CRP and IgG and found that, once off all RA medications fully - my ANA had turned positive at last. So he asked me to have a lip biopsy and this turned up rude positive for each gland removed. Only in January of this year another rheum said I did not have a CT disease of any sort. End of.

So please never give up until you get proper abusers - in fact it may help you just to diagnose yourself with Sjogren's on the strength of your symptoms and high ESR (if I've remembered this correctly - if not then apologies). There are no treatments anyway apart from symptomatic ones - unless you get extraglandular symptoms or another CT disease or organ involvement.

I know quite a lot of people who have self diagnosed with a connective tissue disease because they have completely negative bloods. And when I read their symptoms I can't believe that they haven't been diagnosed and treated just on good faith. It seems there's a post code lottery regarding how Sjogren's is recognised and treated the world over. The UK. Is certainly not good for SS sufferers even if they are seropositive or meet the criteria for this disease as I do
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