For the last ten years I have been attending professor Bruce at Manchester Royal Infirmary. He actually diagnosed Lupus after I had a heart attack a heart and has been outstanding . I travel some distance to attend his clinic and you must have a referral and his clinics are very busy and he takes time to listen .
You say you have to travel a distance to see Prof Bruce. How far? Were you blocked from seeing him? Were there others about but you stuck out for him?
How did you get the referral? Any tips. Note my surgery are not co operating with me, I think I have TIMEWASTER on my notes which is the only guess I have for their unhelpfulness. But, as we know on here we can get ignored for ages.
Anyway, please help if you can. Going to try for Monday so any help before then will be so so appreciated.
I see Prof Bruce at Manchester Royal and cannot recommend him highly enough. I was seeing a Rheumatologist at my local hospital but he had the courage to say he had gone as far as he could with my Lupus so he referred me to the Prof who is a Lupus specialist. He has made some decisions about my treatment and I await a response from it. Waiting for Rituximub to kick in
DaleDiva, thanks so much. Another mention of Prof Bruce. I am revving up to try to get an early apt with a senior gp on Monday or asap to ask for referral to him.
I shall let you all know how things go, especially being armed with my patient Rrights curtesy of the CAB site via an amazing person on this site.
I have had a few Rituximab infusion with the result of no lupus pain but still got osteo pain and recently developed Sorgerns but have had no adverse effects from the infusion and as I say the relief from no lupus pain is a joy .I will see Prof Bruce s clinic shortly
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