What/who can help and getting correct diagnosis and treatment.
Sufferers With PMRGCAuk: What/who can help and... - PMRGCAuk
Sufferers With PMRGCAuk
Diagnosis is normally made by a GP on the basis of your symptoms. Bloods will be taken and often CRP and ESR blood tests will show high inflammation levels. Tap on FAQs on this page to read around the condition. If you think your symptoms fit fill in your registration giving as much detail about your symptoms as you can, this leads to better answers to any questions you may have.
This might help your friend -and you understand a bit more -
Although GPs should be able to diagnose PMR, it in fact is not that easy. It is really a matter of discounting everything else. Raised inflammation markers may give a clue. Also taking steroids for a week and getting a magical improvement in symptoms can also point to PMR. My GP said I had a virus. That went on for three months. In the end I could hardly get out of bed. I went privately to a rheumatologist who diagnosed PMR in about thirty seconds.
Wow, thank you very much. This is so helpful.
Do you think you might have PMR? People on this board have a wealth of knowledge to help if you need it.
I have replied to your last message but it doesn’t seem to have gone through. My enquiries are for a friend who doesn’t use the internet.
thanks for letting me know. Has your friend seen a doctor?
I don’t think you are getting my replies??
can you see your replies?
i can see three replies. I sent a more detailed message to include a brief account of my husband’s illness which has been well managed for years. I don’t think that one reached you. It isn’t on my view but never mind.