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Are Toe sores part of Bechets?
Hi there, Does anyone else get little sores between toes and belive them to be part of Bechets? I saw a new Dr Rheumatologist today who thinks it more likely a fungal thing. She admitted to not having many or any other Bechets patients on her book. The sores sometimes look like a spot other times
Hi there, Does anyone else get little sores between toes and belive them to be part of Bechets? I saw a new Dr Rheumatologist today who thinks it more likely a fungal thing. She admitted to not having many or any other Bechets patients on her book. The sores sometimes look like a spot other times
Icefire
in
Behçet's UK
6 months ago
Lost hearing, vertigo and now rash is this?
I hope someone can help me. I was diagnosed with MCAS in 2015 at Guys and St Thomas then discharged when the drugs started to work. I’ve been in and out of hospital for chronic IC and unexplained gallbladder inflammation which was extremely painful on numerous occasions. Every time I go in I end up
I hope someone can help me. I was diagnosed with MCAS in 2015 at Guys and St Thomas then discharged when the drugs started to work. I’ve been in and out of hospital for chronic IC and unexplained gallbladder inflammation which was extremely painful on numerous occasions. Every time I go in I end up
Redfleur
in
The UK Mastocytosis Support Group
6 months ago
Morphea treatment - PUVA or triamcinolone injections?
hello, looking for a bit of advice as I was diagnosed with Morphea a few months ago. I’m under the care of dermatology department. It affects my whole left arm, part of my rib cage and some of my right arm. The worst area is around my left wrist where the skin is particularly tight around the joint
hello, looking for a bit of advice as I was diagnosed with Morphea a few months ago. I’m under the care of dermatology department. It affects my whole left arm, part of my rib cage and some of my right arm. The worst area is around my left wrist where the skin is particularly tight around the joint
Katie46
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
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red inflamed area around my eye
hi there, I use Latanoprost and Dorzolamide eye drops following a closed angle glaucoma last year. Recently the area around my eye has become very red and inflamed and itchy. Has this happened to anyone else? My doctor gave me steroid cream which has helped a bit. Thanks
hi there, I use Latanoprost and Dorzolamide eye drops following a closed angle glaucoma last year. Recently the area around my eye has become very red and inflamed and itchy. Has this happened to anyone else? My doctor gave me steroid cream which has helped a bit. Thanks
Belladoodle
in
Glaucoma UK
7 months ago
care help for very thin skin.
I have had very thin for years due to asthma meds,in the past few years I have tripped over the prop pavement and my handbag resulting in deep wounds needing nurses dressings at clinics. My are have been thin longer as a young women I used a lot of steroid cream for a skin condition,not as bad as legs
I have had very thin for years due to asthma meds,in the past few years I have tripped over the prop pavement and my handbag resulting in deep wounds needing nurses dressings at clinics. My are have been thin longer as a young women I used a lot of steroid cream for a skin condition,not as bad as legs
maryemma
in
MY SKIN
7 months ago
Has anyone developed Lichen Sclerosus after pelvic radiotherapy?
I was recently diagnosed with Lichen Sclerosus in the genital area. I had chemoradiotherapy 14 years ago for SCC rectum. The cause of LS is not known though trauma to the skin is thought to be one contributory factor. I am extremely worried about this recent development as LS is associated with the development
I was recently diagnosed with Lichen Sclerosus in the genital area. I had chemoradiotherapy 14 years ago for SCC rectum. The cause of LS is not known though trauma to the skin is thought to be one contributory factor. I am extremely worried about this recent development as LS is associated with the development
Hopeful-one
in
Pelvic Radiation Disease Association
7 months ago
Phimosis
Hi all, I’ve had phimosis since I was a teenager due to a scar on my penis. I’m able to retract it completely normally with no problems when flaccid. I can also fully retract it when erect, although it takes a fair bit of resistance and is uncomfortable when retracting, making sex uncomfortable. I’
Hi all, I’ve had phimosis since I was a teenager due to a scar on my penis. I’m able to retract it completely normally with no problems when flaccid. I can also fully retract it when erect, although it takes a fair bit of resistance and is uncomfortable when retracting, making sex uncomfortable. I’
Mainwaring99
in
Men's Health Forum (Penis Health)
8 months ago
rash for 5 months now
hi I’ve had an all over body rash the past 5 months and dermatologist is convinced is because of a virus. No signs of it improving. I’m so worn out with it now. Antihistamines are doing nothing and neither is the steroid cream. Please give some advice what else this could be. They are flat pink spots
hi I’ve had an all over body rash the past 5 months and dermatologist is convinced is because of a virus. No signs of it improving. I’m so worn out with it now. Antihistamines are doing nothing and neither is the steroid cream. Please give some advice what else this could be. They are flat pink spots
Lainey34
in
EFA
8 months ago
pink patches on skin
Hi I am 44 days post SCT and am at home recovering . I’m feeling quite well . I am 68 and have no other health issues . My blood counts are ok considering it’s not long since I had the transplant . haemoglobin is 94 with the help of some jabs in my stomach Platelets 61 WBC 3.8 Neutrofils
Hi I am 44 days post SCT and am at home recovering . I’m feeling quite well . I am 68 and have no other health issues . My blood counts are ok considering it’s not long since I had the transplant . haemoglobin is 94 with the help of some jabs in my stomach Platelets 61 WBC 3.8 Neutrofils
Tortina
in
MPN Voice
8 months ago
skin issue
I have had CLL for about four years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
I have had CLL for about four years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
BlueJk
in
CLL Support
8 months ago
Grover’s disease
I have had CLL for about five years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
I have had CLL for about five years. I am currently on active surveillance and treatment naive. I had a spinal fusion on July 17 for L4-5 due to Spondylolisthesis. I feel like I’m recovering as well as I can expect from the surgery. My hemoglobin dropped to 10 post surgery so I have been very tired but
BlueJk
in
CLL America Support
8 months ago
Another auto immune condition: Lichen sclerosus
I'm in shock. I've just been diagnosed with another auto-immune condition, just as my PMR seems under control. I was diagnosed with PMR in April 2019, and with a few flares I'm now on 4.5mg prednisone. Lichen sclerosus is an unpleasant condition, mostly post-menopausal women, no known cure, just topical
I'm in shock. I've just been diagnosed with another auto-immune condition, just as my PMR seems under control. I was diagnosed with PMR in April 2019, and with a few flares I'm now on 4.5mg prednisone. Lichen sclerosus is an unpleasant condition, mostly post-menopausal women, no known cure, just topical
HelenDaisy
in
PMRGCAuk
9 months ago
Finally hopefully circumcision
So I'm 56 years old have had tightness of foreskin for years and uncomfortable during sex !! I was diagnosed with diabetes about 5 years ago and it has gradually got worse since then about 3 years ago I spoke to a doctor for the first time and was given steroid cream and I left it there it has got worse
So I'm 56 years old have had tightness of foreskin for years and uncomfortable during sex !! I was diagnosed with diabetes about 5 years ago and it has gradually got worse since then about 3 years ago I spoke to a doctor for the first time and was given steroid cream and I left it there it has got worse
stu202
in
Men's Health Forum (Penis Health)
9 months ago
Hemorrhoids and ibs
Hi firstly happy new year to all and apologies for the long post - I have had bowel related symptoms mainly constipation but sometimes diarrhea as well as bloating and intermittent abdominal pain for most of my life and was told many years ago that it is "probably ibs". I have had a recent FIT test which
Hi firstly happy new year to all and apologies for the long post - I have had bowel related symptoms mainly constipation but sometimes diarrhea as well as bloating and intermittent abdominal pain for most of my life and was told many years ago that it is "probably ibs". I have had a recent FIT test which
Jojams
in
IBS Network
4 months ago
Eczema.
Hi, I was diagnosed with an underactive Thyroid in April 2020. I am currently on 75 mcg of Levothyroxine. In the last couple of months, I have started to devolope patches of eczema. The GP has prescribed me with some steroid cream and I also use Hydromol emollient. However, neither of these products
Hi, I was diagnosed with an underactive Thyroid in April 2020. I am currently on 75 mcg of Levothyroxine. In the last couple of months, I have started to devolope patches of eczema. The GP has prescribed me with some steroid cream and I also use Hydromol emollient. However, neither of these products
BuckyBlush55
in
Thyroid UK
10 months ago
Allergic to the sun?
Hi, I've had lots of things go wrong over time, but this is new. I was doing a little gardening, and I mean a little, on Saturday, I felt my feet tingling in the sunshine but didn't think anything of it. I thought i had prickly heat so sat with my feet in a bucket of icy water put some sudocrem on
Hi, I've had lots of things go wrong over time, but this is new. I was doing a little gardening, and I mean a little, on Saturday, I felt my feet tingling in the sunshine but didn't think anything of it. I thought i had prickly heat so sat with my feet in a bucket of icy water put some sudocrem on
Lulamay7
in
LUPUS UK
11 months ago
how can I suppress stool build up
hello, it’s been a while since I posted here but Hopi g someone can help where no doctor has been able to. My colon is always full of stool despite having 15 plus bowel movements a day. I do not eat much in the hope that might relieve the symptoms. But still stool builds up and makes me feel like
hello, it’s been a while since I posted here but Hopi g someone can help where no doctor has been able to. My colon is always full of stool despite having 15 plus bowel movements a day. I do not eat much in the hope that might relieve the symptoms. But still stool builds up and makes me feel like
GKT1969
in
IBS Network
15 hours ago
alcohol with permanent AF
I am in permanent AF controlled with apixoban and verapamil have never had more than Ihalf a glass of wine probably a week however since being diagnosed have not touched any as am paranoid about making things worse a a chemist told me I was being overcautious when I asked about garlic does any one
I am in permanent AF controlled with apixoban and verapamil have never had more than Ihalf a glass of wine probably a week however since being diagnosed have not touched any as am paranoid about making things worse a a chemist told me I was being overcautious when I asked about garlic does any one
KelliEAnniE
in
Atrial Fibrillation Support
22 hours ago
Treatment changes - Rituximab?
Finally saw my consultant again last week. Think he was quite surprised at how swollen my hands have become and he said I'd done well to keep going. So am feeling a little more positive, though I'm battling through a lot of pain. The steroid jabs I had in my finger and thumb base seem to have given
Finally saw my consultant again last week. Think he was quite surprised at how swollen my hands have become and he said I'd done well to keep going. So am feeling a little more positive, though I'm battling through a lot of pain. The steroid jabs I had in my finger and thumb base seem to have given
whitedog
in
NRAS
2 days ago
microscopic haematuria
so about a month ago i was getting vaginal infections that cause soreness and itchyness as well as burning to wee. It was put down to a UTI and was given antibiotics.i also had pelvic pain on my right side that came and went like a stitch. It never cleared so I ended up have 3 lots of antibiotics. Every
so about a month ago i was getting vaginal infections that cause soreness and itchyness as well as burning to wee. It was put down to a UTI and was given antibiotics.i also had pelvic pain on my right side that came and went like a stitch. It never cleared so I ended up have 3 lots of antibiotics. Every
Jellycat123
in
Bladder Health UK
2 days ago
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