consultant: have waited 3 years for a consultant... - LUPUS UK

LUPUS UK

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consultant

sabine profile image
5 Replies

have waited 3 years for a consultant, now have two and it seems one is miss

diagnosing me again!!!!! does anyone else have problems with some medical

staff not grasping the condition?

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sabine profile image
sabine
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5 Replies
Melinda profile image
Melinda

Yes. I was diagnosed and treated for gout in my hand when i had an infection i suspect caused by lupus. Also a few years ago when i developed a circular rash on my arms, chest and legs, i was told it was ringworm. I pointed out that it was most likely a lupus rash as it was in places that had been most exposed to the sun. They were skeptical. It took eight months and a lot of pain and distress, (they would not treat me till i had a diagnosis), to be referred to a dermatologist to be told what i knew all along. My rash was caused by lupus.

carrie67 profile image
carrie67

Hi

I repeatedly went to my GP with rashes on my face. I was told psorisis and other skin conditions all of which should have improved when the sun came out. Surprise,surprise it got worse in the summer. I started to get bald patches and scabs on my head and was told by yet another GP I had mild alopeica and was sent away again as if it was nothing to worry about. It was when my husband made me make an appointmaent at a PRIVATE BUPA hospital that I was finally listened to and the doctor took a biopsy sent it away and within a short period of time I had been diagnosed with Discoid Lupus and was started on treatment straight away. The main thing I was told was to stay away from ultraviolet light.

I know doctors have to put up with a lot of timewasters but some of us are genuine. If I had been listened to and looked after properly it would not only have saved me the discomfort and worry but also a lot of money.

foxglove profile image
foxglove in reply to carrie67

If you don't mind my asking, what treatment are you on for discoid lupus?

sabine profile image
sabine

Hi carrie67

I totally agree with you ref the attitude that some doctors have with this condition

I have been through the same thing feeling that you are a timewaster when in effect it is the GP's who do not have enough information about lupus and how to diagnose it. It was years before I was put on Plaquinol which suited me. now I have a difference consultant to see for a condition which I beleive is just another symptom of Lupus. Some people have commented about the fact that what suits one person will not suit another where medication is concerned and I have found this to be true. I found the rashes and redness distressing when first diagnosed but something i have got used to handling. MY GP has prescribed Ketopine for scalp rashes ect and I have found this to be very good.

sabine profile image
sabine

Hi Foxglove, I have be re-prescribed with plaquinal with shampoo for my hair condition and cream for my over itchy feet!! thank goodness i now have a new gp that is getting to grips with my lupus diagnosis.

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