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Prednisone for treatment of AIG
I've just been started on Prednisone or Prednisolone, immunosuppressant steroids, for treatment of Autoimmune Gastritis/autoimmune PA. This has recently, within the last few years been shown to possibly heal AIG, although not entirely cure. It is also used to prevention immune system rejection of organ
I've just been started on Prednisone or Prednisolone, immunosuppressant steroids, for treatment of Autoimmune Gastritis/autoimmune PA. This has recently, within the last few years been shown to possibly heal AIG, although not entirely cure. It is also used to prevention immune system rejection of organ
Rexz
in
Pernicious Anaemia Society
6 months ago
steroid reduction
Hi guys I'm tapering using Dorset lady program. Im on week 5 so almost on 3 1/2 from four Im doing really well & noticed on the days I'm on the old dose of 4 mil I'm taking more painkillers . So is my body saying its happy on the lower dose. By the way I was diagnosed with PMR & put on steroids & a
Hi guys I'm tapering using Dorset lady program. Im on week 5 so almost on 3 1/2 from four Im doing really well & noticed on the days I'm on the old dose of 4 mil I'm taking more painkillers . So is my body saying its happy on the lower dose. By the way I was diagnosed with PMR & put on steroids & a
Vito5566
in
PMRGCAuk
6 months ago
exercise tips
Morning folks , was on 15g pred initially with PMR diagnosis, after a couple of weeks and around 60/70 % pain relief , had a weekend of weird symptoms in my head . As a precaution was put on 40g pred awaiting blood results . My CRP was 17 , the GP said in an ideal world it should’ve gone down to less
Morning folks , was on 15g pred initially with PMR diagnosis, after a couple of weeks and around 60/70 % pain relief , had a weekend of weird symptoms in my head . As a precaution was put on 40g pred awaiting blood results . My CRP was 17 , the GP said in an ideal world it should’ve gone down to less
Pastamama
in
PMRGCAuk
6 months ago
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do I start my rescue meds?
Hello all, Diagnosed asthma and Bronchiectasis in December following 3 month chest infection. Got better by being hospitalised and treated with nebs, steroids 14 day antibiotics. on daily fostair and reliever. Had a bad chest developing over the week, and I am starting coughing up yellowish phlegm
Hello all, Diagnosed asthma and Bronchiectasis in December following 3 month chest infection. Got better by being hospitalised and treated with nebs, steroids 14 day antibiotics. on daily fostair and reliever. Had a bad chest developing over the week, and I am starting coughing up yellowish phlegm
BroncoM
in
Asthma Community Forum
6 months ago
How long do floaters last
I have a problem with my eyes.I have seen floaters for three months.I don't know what happened,may be steroids drops and antibiotic drops I 've used cause them.Seemed like these floaters have increased recently.Does anyone have an idea for this?How long does it last?Will it disappear within one or two
I have a problem with my eyes.I have seen floaters for three months.I don't know what happened,may be steroids drops and antibiotic drops I 've used cause them.Seemed like these floaters have increased recently.Does anyone have an idea for this?How long does it last?Will it disappear within one or two
Our-poor-guys
in
Glaucoma UK
6 months ago
Steam inhaler recommendation
I’ve had a chest infection and Sinus infection. On the mend now with help of antibiotics and steroids. I have COPD and Asthma and for the past couple of years if I get a bad cold or some virus it always goes to my chest and Sinus and I end up struggling and needing antibiotics and steroids to recover
I’ve had a chest infection and Sinus infection. On the mend now with help of antibiotics and steroids. I have COPD and Asthma and for the past couple of years if I get a bad cold or some virus it always goes to my chest and Sinus and I end up struggling and needing antibiotics and steroids to recover
Deep-Purple
in
Lung Conditions Community Forum
6 months ago
Update to anyone interested
Hello, still in pain and still struggling to get a correct diagnosis. My long awaited referral with a specialist Rheumatologist in Oxford lead to yet more insistence that I have fibromyalgia. I don't have fatigue, brain fog, depression, any stomach disorders...just pain in the neck, girdles and legs
Hello, still in pain and still struggling to get a correct diagnosis. My long awaited referral with a specialist Rheumatologist in Oxford lead to yet more insistence that I have fibromyalgia. I don't have fatigue, brain fog, depression, any stomach disorders...just pain in the neck, girdles and legs
Creas
in
PMRGCAuk
6 months ago
Not believed
I was sent to Rheumatology last year as my hand keeps swelling and I can’t bend my fingers. This was after many years of other issues but I never put the puzzle together and thought I could have been suffering with an autoimmune disease. I have suffered with Angioedema since 2017, with my face blowing
I was sent to Rheumatology last year as my hand keeps swelling and I can’t bend my fingers. This was after many years of other issues but I never put the puzzle together and thought I could have been suffering with an autoimmune disease. I have suffered with Angioedema since 2017, with my face blowing
Tonkie
in
NRAS
6 months ago
Too low or adrenals struggling?
My partner has been on steroids for 3 years, reducing slowly from 20mg with no flares (he's 72 and before pmr was able to join me on 5 to 6 mile walks in the Dales). He is on the last week of a 7 week taper from 3.5mg to 3mg. We had a wonderful two week Nile cruise in November when he was on 4mg .
My partner has been on steroids for 3 years, reducing slowly from 20mg with no flares (he's 72 and before pmr was able to join me on 5 to 6 mile walks in the Dales). He is on the last week of a 7 week taper from 3.5mg to 3mg. We had a wonderful two week Nile cruise in November when he was on 4mg .
Fudgethecat
in
PMRGCAuk
6 months ago
Alendronic Acid and Methotrexate
I've had PMR for about two years. All symptoms vanished completely as soon as I was put on Prednisolone (15mg per day), but I had a bad experience with trying to reduce, as advised by both GPs and my rheumatologist, by large cliff-edge steps--from 15mg to 12.5mg, then 10mg, all in a very few weeks.
I've had PMR for about two years. All symptoms vanished completely as soon as I was put on Prednisolone (15mg per day), but I had a bad experience with trying to reduce, as advised by both GPs and my rheumatologist, by large cliff-edge steps--from 15mg to 12.5mg, then 10mg, all in a very few weeks.
PressBarVet
in
PMRGCAuk
6 months ago
Nothing helps!
I have bronchiectasis in middle right lobe, left lingual and upper lobes, also eosinophilia & chronic allergic rhinitis,asthma & they think aspergillosis. Been seeing consultant for over 20 years and now everything seems to have stopped working ( antibiotics/steroids) I’m waiting on a bronchoscopy that
I have bronchiectasis in middle right lobe, left lingual and upper lobes, also eosinophilia & chronic allergic rhinitis,asthma & they think aspergillosis. Been seeing consultant for over 20 years and now everything seems to have stopped working ( antibiotics/steroids) I’m waiting on a bronchoscopy that
hnakuru
in
Bronchiectasis Support
6 months ago
Polymyalgia
I am quite new to HealthUnlocked and Polymyalgia, although I did join some time ago for my late husband and his Kidney problems . I became ill with Polymyalgia 2days after my 2nd covid injection Astra Zenica 8/04/21. I started with aches all around my shoulders, I was in the middle of moving house at
I am quite new to HealthUnlocked and Polymyalgia, although I did join some time ago for my late husband and his Kidney problems . I became ill with Polymyalgia 2days after my 2nd covid injection Astra Zenica 8/04/21. I started with aches all around my shoulders, I was in the middle of moving house at
sylla123
in
Vasculitis UK
6 months ago
Daily Mail Tuesday 19th
I've just read Martin Scurr in the Health Section of Tuesday's Daily Mail. It's the second article after the Tinitus question. Surely the answer should be NO, he is right it isn't a cure either but he should be saying nothing other than steroids works just to be clear. https://newspaper.mailplus.co.uk
I've just read Martin Scurr in the Health Section of Tuesday's Daily Mail. It's the second article after the Tinitus question. Surely the answer should be NO, he is right it isn't a cure either but he should be saying nothing other than steroids works just to be clear. https://newspaper.mailplus.co.uk
Estellemac
in
PMRGCAuk
6 months ago
first respiratory appt tips please
Hi, I’m 59, asthma since 50, on luforbec 100/6 2 puffs twice a day, montelukast & fexofenadine. I have a first respiratory appt at the hospital and am wondering what to expect?I’ve had 3 exacerbations in the last year, 2 of which needed steroids. Between the 2nd & 3rd (Aug - Nov) I continued to cough
Hi, I’m 59, asthma since 50, on luforbec 100/6 2 puffs twice a day, montelukast & fexofenadine. I have a first respiratory appt at the hospital and am wondering what to expect?I’ve had 3 exacerbations in the last year, 2 of which needed steroids. Between the 2nd & 3rd (Aug - Nov) I continued to cough
nmcv13
in
Asthma Community Forum
6 months ago
PBC, now cirrhosis
HiHad PBC diagnosed for 5 yrs but Alp up since 2012. Been on Urso for 5 yrs and great. In 2021 my ALT was slightly out of range but ignored by the specialist. GP flagged it up January 2023 and I had an ultrasound just showed enlarged spleen. Fibroscan in April jumped from stage one to bottom of stage
HiHad PBC diagnosed for 5 yrs but Alp up since 2012. Been on Urso for 5 yrs and great. In 2021 my ALT was slightly out of range but ignored by the specialist. GP flagged it up January 2023 and I had an ultrasound just showed enlarged spleen. Fibroscan in April jumped from stage one to bottom of stage
Beatrice110924
in
Sjogren's Support
6 months ago
Metaxalone.
I was diagnosed with PMR September 2023 but I'm unable to have steroids. Due to a heart condition I'm also unable to have Immuno suppresants. My Rheumy has now prescribed Metaxalone for pain relief. Reading the side effects I'm not sure I'm happy to take them as they can affect your kidneys and liver
I was diagnosed with PMR September 2023 but I'm unable to have steroids. Due to a heart condition I'm also unable to have Immuno suppresants. My Rheumy has now prescribed Metaxalone for pain relief. Reading the side effects I'm not sure I'm happy to take them as they can affect your kidneys and liver
Joann63
in
PMRGCAuk
6 months ago
Methotrexate and Covid
I am wondering the same thing. I have covid. Tested positive 2 days ago. Should I take Methotrexate and Humira this week? I have continued with steroids 4 mg daily and statins 10 mg daily
I am wondering the same thing. I have covid. Tested positive 2 days ago. Should I take Methotrexate and Humira this week? I have continued with steroids 4 mg daily and statins 10 mg daily
Larmie
in
NRAS
2 months ago
Back Again
Hello everyone, sorry in advance for the mammoth post. I was last on this forum about 7-8 years ago in 2015/2016 after my previous symptom free asthma flared up badly and left me very sick (back on inhalers, steroids, and multiple hospital admissions). We managed to get my asthma back under control
Hello everyone, sorry in advance for the mammoth post. I was last on this forum about 7-8 years ago in 2015/2016 after my previous symptom free asthma flared up badly and left me very sick (back on inhalers, steroids, and multiple hospital admissions). We managed to get my asthma back under control
Beth_19
in
Asthma Community Forum
2 months ago
Back again
Hi All, I don't know if some will remember me but I was on the group about 6 years ago and lost in total 8 stone in weight once I got maintanence under control. I lost weight following a scary asthma experience and with encouragement from a very supportive and imformative clinician who unfortunately
Hi All, I don't know if some will remember me but I was on the group about 6 years ago and lost in total 8 stone in weight once I got maintanence under control. I lost weight following a scary asthma experience and with encouragement from a very supportive and imformative clinician who unfortunately
Beth_19
Restart June 2024
in
Weight Loss Support
2 months ago
Decision about T3 and T4 dosing
My endo agreed to add T3 to my Levothyroxine last summer. I have been taking 2 x 5mcg T3 and 50mcg T4 for some months. My results are: August 2023 - 2 x 5 mcg T3 plus 50/25mcg alternating T4 TSH 0.19 (0.35-4.94) T4 10 (9-19.1) T3 3.7 (2.4-6) November 2023 2 x 5mcg T3 plus 50mcg T4 TSH 0.05 (0.35
My endo agreed to add T3 to my Levothyroxine last summer. I have been taking 2 x 5mcg T3 and 50mcg T4 for some months. My results are: August 2023 - 2 x 5 mcg T3 plus 50/25mcg alternating T4 TSH 0.19 (0.35-4.94) T4 10 (9-19.1) T3 3.7 (2.4-6) November 2023 2 x 5mcg T3 plus 50mcg T4 TSH 0.05 (0.35
FleetRose
in
Thyroid UK
6 months ago
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