Skin biopsy may help for diagnose along with other tests. I had skin biopsy and was diagnosed for Dermatomysitis. DM has rash on face that similar to lupus.
Totally demoralised after seeing the rheumatologist today π’
He told me I don't have a connective tissue disorder and that my skin rash is a "dermatology problem".
He also told me that I'm depressed and I have 'chronic pain syndrome' and that each is exacerbating the other.
He gave me a letter telling my GP to prescribe antidepressants and to refer me to the pain management service for support - likely in the form of a group!
He also recommended CBT for my 'depression'! π‘
He asked for more bloods - Hep C, Vitamin D and a Coombs test. He said he's quite sure the Coombs test will be negative though. He mentioned it and said "It's another Lupus test - you can look it up".
I left in tears.
As he passed me after he handed my blood form to the HCA taking my blood, he smirked (or maybe it was wind π) and said "Cheerio"!
I kid you not!
I'm so angry, upset and frustrated!
All I can do now is wait for the biopsy result and see if my GP will re-refer me to a different rheumatologist.
I've never been made to feel so bad in all my days!
Hubby was with me and said he didn't like his manner either π’
I have a feeling you may have met this rheumy at Salford there possibly can't be two so rude and arrogant. If it was the same man, he told ' us ' by which he meant fibromyalgia sufferers should get back to work as we are costing thousands. I can only suggest you do as we did and put in a complaint to pals. The more people that put in a complaint then something may get done to stop this bullying. I thought these people are supposed to be in a caring profession unfortunately I feel that the pound signs sometimes get in the way. I am so sorry you have been treated this way as I well know this is very hard to get over. Don't let this person put you down carry on fighting . There are people out there that do care. Good luck xx LottieD
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