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The Itch - PBC or nor PBC - Just because you have PBC doesn't mean you can't itch for other reasons.
We are just recovering from several months of itch hell, those of you who experience the full blown itch will know the experience, Sue has been scratching the worst parts till the skin breaks, getting up in the middle of the night because the itch wakes her up and collapsing in tears occasionally at
We are just recovering from several months of itch hell, those of you who experience the full blown itch will know the experience, Sue has been scratching the worst parts till the skin breaks, getting up in the middle of the night because the itch wakes her up and collapsing in tears occasionally at
JohnMalaney
in
PBC Foundation
7 years ago
Is it return of tuberculosis?
I was diagnosed with pulmonary tuberculosis 2 years back...it was initial stage and I have small amount of fluid on right lung and I completed the treatment..took medicines for 8 months and my x rays were good...but from past few days I am having the same stabbing pain in the left side of chest...my
I was diagnosed with pulmonary tuberculosis 2 years back...it was initial stage and I have small amount of fluid on right lung and I completed the treatment..took medicines for 8 months and my x rays were good...but from past few days I am having the same stabbing pain in the left side of chest...my
shailza
in
Lung Conditions Community Forum
7 years ago
Steroids
Hi does anybody know if you can overdose on steroid cream.
Hi does anybody know if you can overdose on steroid cream.
stargazerlilly
in
MY SKIN
7 years ago
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My skin needs help
Between eczema and being allergic to my own sweat, my skin needs more than an overhaul. My doctor prescribed a steroid cream, it seems to be working. Only hours after applying the cream, I noticed improvement. I'm following my GPS advice, I changed my shower gel, I'm eating less salt, trying to stay
Between eczema and being allergic to my own sweat, my skin needs more than an overhaul. My doctor prescribed a steroid cream, it seems to be working. Only hours after applying the cream, I noticed improvement. I'm following my GPS advice, I changed my shower gel, I'm eating less salt, trying to stay
Lenocker68
in
MY SKIN
7 years ago
Malaria...
My mother diagnosed with malaria and she have vomiting 4 to 5 times what to do for instant relief plz tell me....
My mother diagnosed with malaria and she have vomiting 4 to 5 times what to do for instant relief plz tell me....
Anmol_raj
in
Thyroid UK
7 years ago
T3 and lichen sclerosus
I thought I would let others here know my experience. I was diagnosed with this autoimmune skin condition early in 2016. Throughout the following year I had many flare-ups and threatened flare-ups, treated with a strong steroid cream. Due to this and similar problems I started to look for answers to
I thought I would let others here know my experience. I was diagnosed with this autoimmune skin condition early in 2016. Throughout the following year I had many flare-ups and threatened flare-ups, treated with a strong steroid cream. Due to this and similar problems I started to look for answers to
Valerie0106
in
Thyroid UK
7 years ago
I'm being paranoid but need to ask!
So I'm just about to order my Adrenavive and Metavive as recommended by Dr P and I'm a bit worried about transmission of diseases from the glandulars. The Metavive he has recommended is Porcine and it says it is from UK pigs but the Adrenavive is Bovine and states is comes from cows from NZ or Argentina
So I'm just about to order my Adrenavive and Metavive as recommended by Dr P and I'm a bit worried about transmission of diseases from the glandulars. The Metavive he has recommended is Porcine and it says it is from UK pigs but the Adrenavive is Bovine and states is comes from cows from NZ or Argentina
Munchlet
in
Thyroid UK
7 years ago
Do flares ever completely go away?
Hi. I am still here in autoimmune/Lupus limbo and awaiting a follow up consultation with the rheumatologist. 🙆🏼 For the past 11 months I have had many awful, debilitating symptoms, rashes, ulcers , pins and needles- to name a few. The unpleasant spots and red patches of skin I have had for the duration
Hi. I am still here in autoimmune/Lupus limbo and awaiting a follow up consultation with the rheumatologist. 🙆🏼 For the past 11 months I have had many awful, debilitating symptoms, rashes, ulcers , pins and needles- to name a few. The unpleasant spots and red patches of skin I have had for the duration
Minnskimoo
in
LUPUS UK
7 years ago
Rash uncontrollable
I have had this horrific rash since 5/24, which started with bump on my back that itched badly and frank said looked like a spider bite. It spread to shingle type blisters in a vertical line by 4 days. Primary doc said some kind of virus and have me steroid cream. Got worse, spread to legs. Doc took
I have had this horrific rash since 5/24, which started with bump on my back that itched badly and frank said looked like a spider bite. It spread to shingle type blisters in a vertical line by 4 days. Primary doc said some kind of virus and have me steroid cream. Got worse, spread to legs. Doc took
agapepilgrim
in
My MSAA Community
7 years ago
Just been diagnosed with Hypothyroid
Hi I'm new here. Dr diagnosed me a few weeks ago after initially going with a strange spot rash on arms and legs and backside area. After several blood tests and a urine test was told I was B12 deficient and also had an underactive thyroid which he added was quite low. Started to get worried now
Hi I'm new here. Dr diagnosed me a few weeks ago after initially going with a strange spot rash on arms and legs and backside area. After several blood tests and a urine test was told I was B12 deficient and also had an underactive thyroid which he added was quite low. Started to get worried now
tzannath
in
Thyroid UK
7 years ago
What do I have? Wish I could find out!
In September I thought I had a bug bite on my right ankle. By October this rash was all over my body from my neck down. Itching was so very intense. It kept me up at night, would bleed from scratching. I thought at first perhaps it was an allergic reaction to soap, shampoo, food. I tried very over
In September I thought I had a bug bite on my right ankle. By October this rash was all over my body from my neck down. Itching was so very intense. It kept me up at night, would bleed from scratching. I thought at first perhaps it was an allergic reaction to soap, shampoo, food. I tried very over
beckyheth
in
LUPUS UK
7 years ago
Anyone else w/ CLL getting rashes? I need your feedback
I'm wondering how many people with CLL is getting rashes on their shins of their legs, whether their treatment was with FCR or inbru? I've been in remission for almost 10 years now and have been battling this rash for almost all of it. I would love to get anyone's feed back since my 6 month checkup is
I'm wondering how many people with CLL is getting rashes on their shins of their legs, whether their treatment was with FCR or inbru? I've been in remission for almost 10 years now and have been battling this rash for almost all of it. I would love to get anyone's feed back since my 6 month checkup is
Loulou46
in
CLL Support
7 years ago
Update on seeing new auto-immune interest G.P.
Following on from my previous post about not feeling right, despite being on B12 jabs for 6 months after my P.A. diagnosis, and wanting someone to listen and not tell me that I was just stressed and depressed. I think I've found a half decent G.P. at last. He listened to me, gave me a head to toe exam
Following on from my previous post about not feeling right, despite being on B12 jabs for 6 months after my P.A. diagnosis, and wanting someone to listen and not tell me that I was just stressed and depressed. I think I've found a half decent G.P. at last. He listened to me, gave me a head to toe exam
topazrat
in
Pernicious Anaemia Society
7 years ago
Just diagnosed with pbc
Hello all. I am 46 and female. I was just diagnosed with pbc. My ama level is 2.3. My biopsy shows inflammation in liver but no scarring yet so... (early stage). My alkaline phosphatate is 350. My alt is 126 and my ast is 117. I had a positive Ana also but low titer. My doctor thinks I may also have
Hello all. I am 46 and female. I was just diagnosed with pbc. My ama level is 2.3. My biopsy shows inflammation in liver but no scarring yet so... (early stage). My alkaline phosphatate is 350. My alt is 126 and my ast is 117. I had a positive Ana also but low titer. My doctor thinks I may also have
Vera70
in
PBC Foundation
7 years ago
Possible milk allergy?
Hi, I'm looking for some advice on milk allergies. I am in my 40's have had asthma, eczema, hay fever, dust mite and allergies to various animals pretty much my whole life but its always been manageable and never that severe. I don't drink milk and limit my dairy intake for ethical reasons and have done
Hi, I'm looking for some advice on milk allergies. I am in my 40's have had asthma, eczema, hay fever, dust mite and allergies to various animals pretty much my whole life but its always been manageable and never that severe. I don't drink milk and limit my dairy intake for ethical reasons and have done
sarahlou3006
in
EFA
7 years ago
Vulvic pain - Lichen Sclerosis and Vaginismus have been diagnosed but I wonder if that's not all I have. Maybe I have other conditions too.
I wanted to share my story with people. I am 28 and with the same boyfriend that I lost my virginity with three years ago and I am in pain every time we have sex so i rarely enjoy it. It is hard to talk, I find that talking about it makes my self esteem take a huge hit but I had to work through the low
I wanted to share my story with people. I am 28 and with the same boyfriend that I lost my virginity with three years ago and I am in pain every time we have sex so i rarely enjoy it. It is hard to talk, I find that talking about it makes my self esteem take a huge hit but I had to work through the low
ESWright
in
Sexual Health Matters
7 years ago
Vulvic pain - Lichen Sclerosis and Vaginismus have been diagnosed but I'm unsure if that's all I have or if I have other conditions too.
I wanted to share my story with people. I am 28 and with the same boyfriend that I lost my virginity with three years ago and I am in pain every time we have sex so i rarely enjoy it. It is hard to talk, I find that talking about it makes my self esteem take a huge hit but I had to work through the low
I wanted to share my story with people. I am 28 and with the same boyfriend that I lost my virginity with three years ago and I am in pain every time we have sex so i rarely enjoy it. It is hard to talk, I find that talking about it makes my self esteem take a huge hit but I had to work through the low
ESWright
in
Pelvic Pain Support Network
7 years ago
Hydroxychloroquine DLE
Is there alternative treatments that are not so potent as Hydroxychloroquine for Discoid Lupus( that is not Chronic) As The steroid cream works on the Face but the Shoulder on old BCG area from years ago which was recently Biopsied is extremely Itchy in the evening i would be grateful for some advice
Is there alternative treatments that are not so potent as Hydroxychloroquine for Discoid Lupus( that is not Chronic) As The steroid cream works on the Face but the Shoulder on old BCG area from years ago which was recently Biopsied is extremely Itchy in the evening i would be grateful for some advice
Advice1
in
LUPUS UK
7 years ago
Where to start, who to see?
Hello, My daughter has just been diagnosed with discoid lupus, so we are slowly coming to terms with all that this will entail for her. She's 9 years old and has had skin problems and horrible rashes whenever we have visited sunny countries, we finally had our diagnosis after being bounced between dermatologist
Hello, My daughter has just been diagnosed with discoid lupus, so we are slowly coming to terms with all that this will entail for her. She's 9 years old and has had skin problems and horrible rashes whenever we have visited sunny countries, we finally had our diagnosis after being bounced between dermatologist
Tommyw
in
LUPUS UK
7 years ago
Red dry skin patches with SS.
Does anyone with SS or RA get red dry patches on skin that isn't Psoriasis? My derm says it not that and just some type of inflammation but doesn't know what and gave me low dose steroid cream to put on which helps but it doesn't get rid of it. It's always pink and sometimes flares and gets little
Does anyone with SS or RA get red dry patches on skin that isn't Psoriasis? My derm says it not that and just some type of inflammation but doesn't know what and gave me low dose steroid cream to put on which helps but it doesn't get rid of it. It's always pink and sometimes flares and gets little
wsjkcj1
in
The Australian Sjögren's Syndrome Association
8 years ago
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