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Hydrocortisone topical
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Moon face woes
Since being diagnosed with adrenal failure in March, I've been on hydrocortisone daily. Initially it was 20mg/day and I've now reduced it down to 10mg/day. I also take Seretide, was 250/50 x 2 puffs am/pm. Now I've been able to reduce that down to 1 puff am/pm because my lung function is so much better
Since being diagnosed with adrenal failure in March, I've been on hydrocortisone daily. Initially it was 20mg/day and I've now reduced it down to 10mg/day. I also take Seretide, was 250/50 x 2 puffs am/pm. Now I've been able to reduce that down to 1 puff am/pm because my lung function is so much better
Hidden
in
Asthma Community Forum
11 years ago
Allergic to the sun
Does anyone else have this problem & is it fibro related? A couple of weeks ago I went outside in a Tshirt to hang out the washing, I was only out for about 10 mins. A couple of days later I came out with a really nasty rash on my arms like I had really been burnt, doctor gave me hydrocortisone cream
Does anyone else have this problem & is it fibro related? A couple of weeks ago I went outside in a Tshirt to hang out the washing, I was only out for about 10 mins. A couple of days later I came out with a really nasty rash on my arms like I had really been burnt, doctor gave me hydrocortisone cream
glochessum
in
Fibromyalgia Action UK
11 years ago
How do I know if rash is due to PBC?
I was diagnosed w/PBC 5 months ago, 2013. In 2009 I developed a very itchy rash on each side of my collar bone. A dermatologist prescribed hydrocortisone cream & anti-itch pills, & it went away in a few days. This same exact rash, in same exact location, has occurred 4 yrs. later. The skin is red & inflamed
I was diagnosed w/PBC 5 months ago, 2013. In 2009 I developed a very itchy rash on each side of my collar bone. A dermatologist prescribed hydrocortisone cream & anti-itch pills, & it went away in a few days. This same exact rash, in same exact location, has occurred 4 yrs. later. The skin is red & inflamed
WendyMarie
in
PBC Foundation
11 years ago
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Rituximab experience
Full of high hopes for my new treatment, I went along to the infusion unit at the Western General in Edinburgh to have my first dose of rituximab. Over the last couple of years I've had bad reactions to methotrexate and sulfasalazine, no response to Cimzia or Humira and consequently RA has been progressing
Full of high hopes for my new treatment, I went along to the infusion unit at the Western General in Edinburgh to have my first dose of rituximab. Over the last couple of years I've had bad reactions to methotrexate and sulfasalazine, no response to Cimzia or Humira and consequently RA has been progressing
Sailaway
in
NRAS
11 years ago
Vasculitis (Churg-Strauss Syndrome) - my story so far .. 11 weeks on
I thought that I would share my recent, and still ongoing, experience of vasculitis which has made me realise just how fortunate I have been in getting a speedy diagnosis and first class treatment. (BTW: I have a degree in Physics so am used to doing tests and monitoring trends etc, so this write
I thought that I would share my recent, and still ongoing, experience of vasculitis which has made me realise just how fortunate I have been in getting a speedy diagnosis and first class treatment. (BTW: I have a degree in Physics so am used to doing tests and monitoring trends etc, so this write
JontyW
in
Vasculitis UK
11 years ago
Active Duty US Marine With AMN
My story began when my 7-year-old nephew was diagnosed with ALD due to the symptoms he had and through all the tests that he had done the summer of 2007. Once my nephew’s mother, Audrey, was informed this disease was hereditary, my immediate family (siblings and mother) received the same testing to conclude
My story began when my 7-year-old nephew was diagnosed with ALD due to the symptoms he had and through all the tests that he had done the summer of 2007. Once my nephew’s mother, Audrey, was informed this disease was hereditary, my immediate family (siblings and mother) received the same testing to conclude
Chacho308
in
Leukodystrophy Support
11 years ago
Rash on back of knee and arms
Hello all I have a rash that appears on my arms and behind my knees. I am not on any new meds, not changed washpowder, soap etc. Doctor did give me steroid cream which seem to help but now they are back. They only seen to rich when I get hot. I don't think that it is heat rash I have had this before
Hello all I have a rash that appears on my arms and behind my knees. I am not on any new meds, not changed washpowder, soap etc. Doctor did give me steroid cream which seem to help but now they are back. They only seen to rich when I get hot. I don't think that it is heat rash I have had this before
patrisha
in
Fibromyalgia Action UK
11 years ago
Ursodoxycholic tabs
Hi all, After reading answers to my question regarding itching I went to my GP on Friday and got him to prescribe these tablets,my question is:- how long before I see any improvement with iitching, so far no change at all. Really getting me down there's just no relief from it, I'm using double base
Hi all, After reading answers to my question regarding itching I went to my GP on Friday and got him to prescribe these tablets,my question is:- how long before I see any improvement with iitching, so far no change at all. Really getting me down there's just no relief from it, I'm using double base
Gizmo326
in
British Liver Trust
11 years ago
First Enbrel Blood Test Result after three injections. Sorry, a ramble.
I am, I have to say, upset :-(. I have just had a little cry although my other fingers and knee (the ones not recently injected! or not since January) told me quite obviously, there is active inflammation there at the mo. Red hot knuckles which are stiff. They are the knuckles of a flare and I saw
I am, I have to say, upset :-(. I have just had a little cry although my other fingers and knee (the ones not recently injected! or not since January) told me quite obviously, there is active inflammation there at the mo. Red hot knuckles which are stiff. They are the knuckles of a flare and I saw
Neonkitty
in
NRAS
11 years ago
New here. Test results diagnose Hashi's. Any advice/comments greatly appreciated.
Hi all, I have been lurking and reading here since March but this is my first post. I will apologise in advance as it will probably be long and rambling (foggy brain), so thanks in advance if you manage to bear with me through it all. Since a bout of laryngitis around 8 years ago when I lived
Hi all, I have been lurking and reading here since March but this is my first post. I will apologise in advance as it will probably be long and rambling (foggy brain), so thanks in advance if you manage to bear with me through it all. Since a bout of laryngitis around 8 years ago when I lived
flying_swallow
in
Thyroid UK
11 years ago
Has anyone got any advice for lichen sclerosus please
Although I am using steroid cream, it seeme a long road and I would be interested if there is another treatment
Although I am using steroid cream, it seeme a long road and I would be interested if there is another treatment
Frappet
in
MY SKIN
11 years ago
Full Zante holiday update!! ( it may be long??!!)
Well on the 9TH of May set off at 3.34 am in the morning to travel to a car park north of Birmingham airport at Garretts green,( have used the car park three times before but not for over five years!).. well lots of building and development occurred and we had had trouble finding it!!, we were behind
Well on the 9TH of May set off at 3.34 am in the morning to travel to a car park north of Birmingham airport at Garretts green,( have used the car park three times before but not for over five years!).. well lots of building and development occurred and we had had trouble finding it!!, we were behind
Hidden
in
NRAS
11 years ago
Mtxate injections: rash
Well, I went to GP about the rash I reported earlier this week. Diffuse, red pinpoints. The GP phoned rheumatology who suggested I stop methotrexate completely and wait til my next appointment - which isnt for a while. Unhelpful. Then she phoned dermatology who agreed to see me this afternoon. Was looked
Well, I went to GP about the rash I reported earlier this week. Diffuse, red pinpoints. The GP phoned rheumatology who suggested I stop methotrexate completely and wait til my next appointment - which isnt for a while. Unhelpful. Then she phoned dermatology who agreed to see me this afternoon. Was looked
cathie
in
NRAS
11 years ago
Hello, amazed to fnd a form relatng to this!
Eight and half years ago I came off HRT. Six weeks later my skin n my back was covered n red extremely itchy lump which spread then on arms and legs. My GP thought it was exzema and could not understand why, he prescribed some steroid ointment. This made me scratch even more and the patch on back became
Eight and half years ago I came off HRT. Six weeks later my skin n my back was covered n red extremely itchy lump which spread then on arms and legs. My GP thought it was exzema and could not understand why, he prescribed some steroid ointment. This made me scratch even more and the patch on back became
Cairnperson
in
Nodular Prurigo International
11 years ago
cannulas
not 100% sure why, but recently, since i've had a lot of cannulas in i have been really really struggling with them. I think part of the issue is that i find cannulas in my hands to be absolute agony (to the extent i cannot move my arm or hand at all, cant tolerate people even moving my fingers, sometimes
not 100% sure why, but recently, since i've had a lot of cannulas in i have been really really struggling with them. I think part of the issue is that i find cannulas in my hands to be absolute agony (to the extent i cannot move my arm or hand at all, cant tolerate people even moving my fingers, sometimes
Hidden
in
Asthma Community Forum
11 years ago
Advice desperately needed - I have stopped my medication!
I desperately need advice before I speak to my GP tomorrow morning. Sorry for the length of this. In July 2008 Dr Peatfield diagnosed me as low adrenals/low T3 and T4 (urine testing: T3 below range, T4 very low normal, saliva cortisol below range). He thought my problems stemmed from weak adrenals
I desperately need advice before I speak to my GP tomorrow morning. Sorry for the length of this. In July 2008 Dr Peatfield diagnosed me as low adrenals/low T3 and T4 (urine testing: T3 below range, T4 very low normal, saliva cortisol below range). He thought my problems stemmed from weak adrenals
Arkledessie
in
Thyroid UK
11 years ago
Day 6 - Failed!
Well I turned up at the hospital for my dermatology appointment looking a bit of a state and suddenly I am getting a result from staff (staff being nurse rather than the doctor as she flitted about but never actually spoke to me this time). The nurse was fantastic and sat and listened and took notes
Well I turned up at the hospital for my dermatology appointment looking a bit of a state and suddenly I am getting a result from staff (staff being nurse rather than the doctor as she flitted about but never actually spoke to me this time). The nurse was fantastic and sat and listened and took notes
max_downes
in
MY SKIN
11 years ago
Any advice for when i go and see the endo on tuesday
I am back at the endo on tue afternoon, Like lots of other people i struggle on a daily basis, I take levothyroxine 125 mcg, hydrocortisone, ddavp, growth hormone injection every day. By the way my pituitary gland doesnt work so therefore neither does my thyroid. A few months ago i was started on colecalciferol
I am back at the endo on tue afternoon, Like lots of other people i struggle on a daily basis, I take levothyroxine 125 mcg, hydrocortisone, ddavp, growth hormone injection every day. By the way my pituitary gland doesnt work so therefore neither does my thyroid. A few months ago i was started on colecalciferol
saints
in
Thyroid UK
11 years ago
Phased return to work almost over.....
Hi everyone! Thought id write an update. Ive been on a phased return to work as a midwife over the last 6 weeks. Since starting the t3/t4 combo i had started to feel slightly better, much brighter mentally ( though memory is still poor) and my clinical signs became much more stable. I did still
Hi everyone! Thought id write an update. Ive been on a phased return to work as a midwife over the last 6 weeks. Since starting the t3/t4 combo i had started to feel slightly better, much brighter mentally ( though memory is still poor) and my clinical signs became much more stable. I did still
babycatcher7572
in
Thyroid UK
11 years ago
Diagnosis of vulvadynia but think I have trapped nerve..
I am a 49 year old and about 18 months ago had a severe bout of cystitis which I didn't recover properly from despite antibiotics. About 3 months later I was still experiencing what felt like pressure on the bladder and had an ultrasound of my bladder but was told everything was okay. The next symptoms
I am a 49 year old and about 18 months ago had a severe bout of cystitis which I didn't recover properly from despite antibiotics. About 3 months later I was still experiencing what felt like pressure on the bladder and had an ultrasound of my bladder but was told everything was okay. The next symptoms
juliapiper
in
Pelvic Pain Support Network
11 years ago
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