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Experiences with
Hydrocortisone / Tretinoin / Hydroquinone cream
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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
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
Oilatum
Jo from BLF mentioned aqueous cream yesterday and to be carefull because of something it contains, unfortunately can't get to the post to see what it was, anyhow i called in Lloyds pharmacy this morning just out of curiosity, for people who suffer from eczema as well as respiratory problems they highly
Jo from BLF mentioned aqueous cream yesterday and to be carefull because of something it contains, unfortunately can't get to the post to see what it was, anyhow i called in Lloyds pharmacy this morning just out of curiosity, for people who suffer from eczema as well as respiratory problems they highly
azaard
in
Lung Conditions Community Forum
11 years ago
Aqueous cream and eczema advice.
Hi Allergy UK have some information on their website about the use of aqueous cream for eczema. NICE (National Institute for Clinical Excellence) issued guidelines in 2010 against its use when people have eczema but it is apparently still being used. Aqueous contains sodium lauryl sulphate which
Hi Allergy UK have some information on their website about the use of aqueous cream for eczema. NICE (National Institute for Clinical Excellence) issued guidelines in 2010 against its use when people have eczema but it is apparently still being used. Aqueous contains sodium lauryl sulphate which
Jo_BLFHelpline
British Lung Foundation
in
Lung Conditions Community Forum
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
increased meds
Hi all, After seeing my consultant earlier this month the only meds I was on were:- Propanolol,co-trimoxazole. I have recently been to see my Gp regarding itching and swelling in my ankles and feet ( Oedema) he now out me on spironolactol, fexofenadene,and Fucibet cream, The itching has not
Hi all, After seeing my consultant earlier this month the only meds I was on were:- Propanolol,co-trimoxazole. I have recently been to see my Gp regarding itching and swelling in my ankles and feet ( Oedema) he now out me on spironolactol, fexofenadene,and Fucibet cream, The itching has not
Gizmo326
in
British Liver Trust
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
retinoic acid
has any one heard any more information about the research done with retinoc acid ( a derivative of vit A ) as healing lung damage in emphysema ? Its research done at Kings College by prof Malcolm Maden.
has any one heard any more information about the research done with retinoc acid ( a derivative of vit A ) as healing lung damage in emphysema ? Its research done at Kings College by prof Malcolm Maden.
mishawaka
in
Lung Conditions Community Forum
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
PUPPP / PEP / itchy rash
I have had itching all over my body, except feet, hands and face, for about the last three weeks. It started off without any rash, which was concerning in case it was Obstetric Chlorestasis, but two blood tests do not indicate any cause for concern in that respect, thankfully. However, the itch is getting
I have had itching all over my body, except feet, hands and face, for about the last three weeks. It started off without any rash, which was concerning in case it was Obstetric Chlorestasis, but two blood tests do not indicate any cause for concern in that respect, thankfully. However, the itch is getting
LunaD
in
Pregnancy and Parenting Support
11 years ago
bet you wondered where ol' itchy bear had gone to!!...
... finally got to see ma dermatologist last week,she was very nice and of course I had no rash to show her ,she thinks my nervious system is overkeyed and she suggested upping my amitryptiline and she would also refer me to one of the dermatologists at York hospital to havew me try ultra light treatment
... finally got to see ma dermatologist last week,she was very nice and of course I had no rash to show her ,she thinks my nervious system is overkeyed and she suggested upping my amitryptiline and she would also refer me to one of the dermatologists at York hospital to havew me try ultra light treatment
electricjaws
in
Fibromyalgia Action UK
11 years ago
Saliva test.
Hi I have tried to work out if I need hydrocortisone or Isocort is enough, Does somebody know? They seem pretty normal to me except for the DHEA. Sample 1 11.4L (12-22) Sample 2 8.1 (5-9) Sample 3 6.4 (3-7) Sample 4 2.7 (1-3) Total daily cortisol 28.6 (21-41) DHEA Sample
Hi I have tried to work out if I need hydrocortisone or Isocort is enough, Does somebody know? They seem pretty normal to me except for the DHEA. Sample 1 11.4L (12-22) Sample 2 8.1 (5-9) Sample 3 6.4 (3-7) Sample 4 2.7 (1-3) Total daily cortisol 28.6 (21-41) DHEA Sample
roslin
in
Thyroid UK
11 years ago
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