Advice please - 1st post: Diagnosed last July: CRP... - PMRGCAuk

PMRGCAuk

21,317 members40,425 posts

Advice please - 1st post

cribbager profile image
18 Replies

Diagnosed last July: CRP 65mg/normal range 0-5. Went private as no-one at surgery could speak to me for 10 days. 15mg Prednisolone - magic, immediately. GP returned, and cut to 10mg after 10 days, 'reduce by 1 mg per 2 weeks as tolerated'. I got down to 7mg but not effective from the 10mg onwards. I knew nothing but have learnt lots from this forum. I've had 2 phone conversations with him plus one text when I said I was going up to 9. Still achy painful thighs so 6 weeks ago I went up to 12mg which worked and I'm decreasing by .5mg each 2 weeks. It's working. My question is so many of you speak of regular consultations/blood tests/ contacts with rheumatologists /advice re vitamins etc- should I expect this or carry on (I've written to GP to set out my position and await his reply)?

Written by
cribbager profile image
cribbager
To view profiles and participate in discussions please or .
Read more about...
18 Replies
jinasc profile image
jinasc

Starter for 10. DR Sarah Mackie is a Leading Researcher into PMR & GCA and is also a Trustee on PMR GCA UK>

healthunlocked.com/pmrgcauk...

Others will be along soon with advice.

Two things:

Write two copies down and give one to your GP.

TAKE SOMEONE WITH YOU FOR THE CONSULTATION.

cribbager profile image
cribbager in reply tojinasc

Thanks - such a quick response

DorsetLady profile image
DorsetLadyPMRGCAuk volunteer

Have a browse through this for general info - healthunlocked.com/pmrgcauk...

And this for treatment of PMR from charity website -

pmrgca.org.uk/wp-content/up...

cribbager profile image
cribbager in reply toDorsetLady

Many thanks - I've previously browsed the 1st, and on your previous advice 'bought the book' which I'm reading but not come across 2nd suggestion so will read it later - thanks, you're so often helpful

DorsetLady profile image
DorsetLadyPMRGCAuk volunteer in reply tocribbager

You’re welcome - the more you know, the better you cope. It’s not easy early days, but the more experienced you become, the more you feel in control. Good luck.

cribbager profile image
cribbager in reply toDorsetLady

Thanks again

piglette profile image
piglette

Around 75% of people with PMR never see a rheumatologist. I had to get PMR diagnosed privately by a rheumatologist as my GP kept saying it was a virus. I was given steroids and vitamin D with calcium which are recommended and a Dexascan to check bone density. I had to fight for that. I think basically that is all you need. I had blood tests every three months and now only if I have problems. I think I would move to reducing every four weeks when you get to 10mg.

cribbager profile image
cribbager in reply topiglette

Many thanks - yes, think I'll slow down as 10mg didn't work too well initially. Thanks

piglette profile image
piglette in reply tocribbager

If you have any problems STOP reducing, PMR always wins!

cribbager profile image
cribbager in reply topiglette

Thanks. I've gathered that from all the stories and advice I've read on here since finding this forum

Zebedee44 profile image
Zebedee44

Welcome Cribbager, In five years of managing PMR I have learned more and had better advice from this forum than any doctors. I seldom have my bloods tested and I just soldier on in my own way with tapering the pred according to how much pain I am in. I saw Rod Hughes in Chertsey privately after three years but nothing changed other than better understanding of the complexity of PMR, then I saw a rheumatologist last year at my local hospital who prescribed leflunomide to help reduce the pred dose but didn’t advise me on side effects or adrenal insufficiency and didn’t do bloods.

Without this forum I would feel very lonely and unsupported as I journey through this experience. The folk here have personal experience of PMR and GCA and know far more about it than the medics, well that’s my experience.

cribbager profile image
cribbager in reply toZebedee44

Thank you Zebedee - I fully agree re the folk on this fantastic forum. All the best in your journey

Mazxstitch profile image
Mazxstitch

I was diagnosed with PMR April 2019, started on 15mg and after 15 months of "reduce 1mg every 2 weeks" and yo-yoing I was down to 10 mg. Found this forum and have used tapering plans ever since. I am presently on 5.5 mg. Only reducing .5mg every 5 weeks and feel much better.

cribbager profile image
cribbager in reply toMazxstitch

Thank you - I think the main message I'm getting is to listen to my body and be very slow in reducing

Sharitone profile image
Sharitone

Blood tests: yes, you would expect regularish blood tests while you are on steroids, particularly the early days. Vitamins: most of us get prescribed Vit D3 along with a calcium supplement, though some do not need it. Others get given Folic Acid (Vit B9), usually along with methotrexate. Otherwise, vitamins are not usually offered s far as I know; you have to do your own research and decide. Many people on calcium supplements take Vit K2.

cribbager profile image
cribbager in reply toSharitone

Thank you for your advice and information. This is such a helpful forum!

HeronNS profile image
HeronNS

Another experience: diagnosed by a new doctor in 2015 after over a year of increasing pain. 15 mg - miracle! After one month told to taper by 1 mg per week - BUT to stop reducing if there was any return of symptoms. This happened at 9 mg. On-line I found a forum where I learned I could increase my dose if pain came back. Went back to 10. Got slow taper plan, asked doctor what she thought, although I planned to use it anyway. She said I should give it a try. At that time, early days, I think I was seeing her once a month, then it was every three months. One day after a couple of years and me at a very low dose she said, see you in a year! She moved away, and I have had a major flare (now subsided) and my new doctor suggests every six months would be good for checking in. I am, of course, much older now, in my mid-70s rather than late 60s, and feeling it.

cribbager profile image
cribbager in reply toHeronNS

Thanks for your time and advice. This forum is so responsive, caring and helpful. I'm learning that I need to listen to my body and take time. Cheers

Not what you're looking for?

You may also like...

Prednisolone Taper Advice Please

After losing sight in one eye, I was diagnosed with GCA & PMR at the end of this July. After a...
Welshmerlin profile image

My next taper - advice please

Hello, I don’t post often but read posts everyday. Diagnosed PMR end Dec 2018, started on 15mg for...

Real problems getting back on track with tapering

I’m 2 years into my PMR journey and recently got down to 5.5 mg pred using one of the slow...
Laineydee profile image

Going backwards...again. 10mg wall? Advice please

Advice please, I’m really struggling. Brief background; PMR symptoms undiagnosed for > 3 years...

Suffering from soreness & tenderness. Have increased Pred but think maybe that's a mistake and I just need to put up with it - any advice?

I've just found this site and reading everyone's posts has been SO helpful. I've been struggling...

Moderation team

SophieMB profile image
SophieMBPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.