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Why don't Doctors recognise the chronic after effects of Meningitis?
Hi Everyone. So I'm sat watching the news and they are talking about the effects of 'Long Covid'. Doctors are actually recognising the chronic symptoms patients are experiencing and planning how to improve their care. Covid has been around how long? How about Doctors listening to the Chronic symptoms
Hi Everyone. So I'm sat watching the news and they are talking about the effects of 'Long Covid'. Doctors are actually recognising the chronic symptoms patients are experiencing and planning how to improve their care. Covid has been around how long? How about Doctors listening to the Chronic symptoms
Emerald8888
in
Meningitis Now
4 years ago
Differences in those with or without a thyroid
One area tends to confound me a bit here. I’m in the US and focused on thyroid cancer and those of us who have had thyroidectomies. This is one of the best thyroid forums around (excellent information, great mods and caring support) and I often refer folks who come to our US thyroid cancer forum here
One area tends to confound me a bit here. I’m in the US and focused on thyroid cancer and those of us who have had thyroidectomies. This is one of the best thyroid forums around (excellent information, great mods and caring support) and I often refer folks who come to our US thyroid cancer forum here
Poniesrfun
in
Thyroid UK
4 years ago
Cellulitis and garments
Should you wear your compression sleeve if you've developed Cellulitis in Lymphedema arm?
Should you wear your compression sleeve if you've developed Cellulitis in Lymphedema arm?
AbbeyMpom
in
LSN
4 years ago
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Biological therapy
Hi I have Rheumatoid arthritis for 46 years. I have had many joint replacements and too numerous treatments to mention, I was on Methotrexate for 20 years, but it damaged my liver, then Azathioprine for 5 years, which was no longer effective. Been on Prednisolone for last 6 months due to Covid
Hi I have Rheumatoid arthritis for 46 years. I have had many joint replacements and too numerous treatments to mention, I was on Methotrexate for 20 years, but it damaged my liver, then Azathioprine for 5 years, which was no longer effective. Been on Prednisolone for last 6 months due to Covid
myranicholls
in
NRAS
4 years ago
PAIN 30 DAYS POST TURP
I had a Turp procedure about a month ago. I was bleeding lightly for about 3 weeks, that finally stopped. However, I'm still getting pain when I urinate. As far as I know I do not have cancer, but I had a pretty large prostate (125 ml). The doctor wanted to do the procedure because i was being hospitalized
I had a Turp procedure about a month ago. I was bleeding lightly for about 3 weeks, that finally stopped. However, I'm still getting pain when I urinate. As far as I know I do not have cancer, but I had a pretty large prostate (125 ml). The doctor wanted to do the procedure because i was being hospitalized
pisdov
in
Prostate Cancer Network
4 years ago
Want to learn about lupron and casodex
I have been doing watchful waiting for 15 years. My Urologist did a TURP operation and the pathology said gleason 3/5. My Doc wants me to do Casodex to start. I have read that any kind of T deprivation can cause weight gain, man boobs, lethargy and heart problems. I have always been a skinny hyper active
I have been doing watchful waiting for 15 years. My Urologist did a TURP operation and the pathology said gleason 3/5. My Doc wants me to do Casodex to start. I have read that any kind of T deprivation can cause weight gain, man boobs, lethargy and heart problems. I have always been a skinny hyper active
fightingsnook
in
Prostate Cancer Network
4 years ago
What next??
Hello. Brand new here! Diagnosed with Stage 4, Gleason 9 PCa during TURP surgery on 10/30/19. Mets to pelvic bones and bladder neck invasion. PSA has always been 2-3. ADT (Lupron and Erleada)has me at PSA of <.03. Confused about what’s next. MO says ride out ADT, urologist wants to remove prostate and
Hello. Brand new here! Diagnosed with Stage 4, Gleason 9 PCa during TURP surgery on 10/30/19. Mets to pelvic bones and bladder neck invasion. PSA has always been 2-3. ADT (Lupron and Erleada)has me at PSA of <.03. Confused about what’s next. MO says ride out ADT, urologist wants to remove prostate and
Canton44
in
Advanced Prostate Cancer
4 years ago
Lyme Disease and hypothyroid?
Hello all As well as being hypothyroid I have sevear Chronic Fatigue. Just to cross things off the list I am working through all the possibilities that might be underpinning my CF. So I had a Lymes (elissa test) and the results state that I have been in contact with the Borrelia Burgdorferi bacterium
Hello all As well as being hypothyroid I have sevear Chronic Fatigue. Just to cross things off the list I am working through all the possibilities that might be underpinning my CF. So I had a Lymes (elissa test) and the results state that I have been in contact with the Borrelia Burgdorferi bacterium
smilingjane
in
Thyroid UK
4 years ago
BANK HOLIDAY HOWLERS
I used to do Antique Collectors fairs Bank Holiday as it in the UK. Thought share some of my favourites comedy moments it lift those on a dreary day or give those some thing to smile about. Used to visit South West Yorkshire lots of lovely people. A customer approached my stall have you got any Turps
I used to do Antique Collectors fairs Bank Holiday as it in the UK. Thought share some of my favourites comedy moments it lift those on a dreary day or give those some thing to smile about. Used to visit South West Yorkshire lots of lovely people. A customer approached my stall have you got any Turps
MrRigatoni
in
Positive Wellbeing During Self-Isolation
4 years ago
Wegners granulomatosis GPA
Hi there, I’m new to this site. Been recently diagnosed in June. Affected my lungs eyes ears. But more importantly affected my prostate. I had a TURP operation which showed dead matter. Then ended up with 2 more operations to resolve a fistula affecting the back passage and the urethra. Currently
Hi there, I’m new to this site. Been recently diagnosed in June. Affected my lungs eyes ears. But more importantly affected my prostate. I had a TURP operation which showed dead matter. Then ended up with 2 more operations to resolve a fistula affecting the back passage and the urethra. Currently
jagjitd
in
Vasculitis UK
4 years ago
Bad nails
Does anyone have problems with their nails? The white part of the nails are getting bigger where the nail is not attached to my finger. The nails are also very thin and brittle so I can’t grow them long I just have to hide it with nail varnish as they look awful.
Does anyone have problems with their nails? The white part of the nails are getting bigger where the nail is not attached to my finger. The nails are also very thin and brittle so I can’t grow them long I just have to hide it with nail varnish as they look awful.
Jolevans
in
LUPUS UK
4 years ago
Skin cancer does NOT only occur in moles‼️
Skin cancer does NOT only occur in moles‼️ The other (non-mole) basic warning signs we suggest you look out for are: 📍A new red or darker colour flaky patch that may be a little raised 📍A new flesh-coloured firm bump 📍An open sore that doesn't heal 📍A spot or sore that continues to itch, hurt
Skin cancer does NOT only occur in moles‼️ The other (non-mole) basic warning signs we suggest you look out for are: 📍A new red or darker colour flaky patch that may be a little raised 📍A new flesh-coloured firm bump 📍An open sore that doesn't heal 📍A spot or sore that continues to itch, hurt
SkcinHQ
Partner
in
Skin Cancer UK
4 years ago
Zytiga users, How much prednisolone do you take?
My father is Gleason 9. Psa 292 at diagnosis. Following orcidectomy and TURP, he's on zytiga plus prednisolone since August 2019. Last week, scary symptoms of low sodium made us rush to the Emergency room. Has anyone else experienced this? Also, how much prednisolone are you taking with your zytiga
My father is Gleason 9. Psa 292 at diagnosis. Following orcidectomy and TURP, he's on zytiga plus prednisolone since August 2019. Last week, scary symptoms of low sodium made us rush to the Emergency room. Has anyone else experienced this? Also, how much prednisolone are you taking with your zytiga
Faithhope11
in
Advanced Prostate Cancer
4 years ago
chronic viral meningitis
hi, I have chronic meningiris..this is my 5 th month, I suffer from all sorts of pain and chronic migraines and headaches. anyone with chronic meningitis?
hi, I have chronic meningiris..this is my 5 th month, I suffer from all sorts of pain and chronic migraines and headaches. anyone with chronic meningitis?
amk2
in
Meningitis Now
4 years ago
Toenails and PsA (there is a photo)
When I first saw the rheumy, he asked about issues with my toenails and I said no. My nails aren’t exactly attractive, but they’ve been the way they are now for so long that I didn’t give it a second thought. My finger nails all have very faint vertical lines with sparse but fairly regular splinter haemorrhages
When I first saw the rheumy, he asked about issues with my toenails and I said no. My nails aren’t exactly attractive, but they’ve been the way they are now for so long that I didn’t give it a second thought. My finger nails all have very faint vertical lines with sparse but fairly regular splinter haemorrhages
Hidden
in
NRAS
4 years ago
Bladder contracture Options?
As a result of PC treatment and a TURP (after radiation, not advised) to correct a brutal catheterization I now have extreme difficulty urinating and at this time can not even get a catheter into my bladder. I have straight caths arriving later today and hope to be able to get one of them to work since
As a result of PC treatment and a TURP (after radiation, not advised) to correct a brutal catheterization I now have extreme difficulty urinating and at this time can not even get a catheter into my bladder. I have straight caths arriving later today and hope to be able to get one of them to work since
spencoid2
in
Prostate Cancer And Gay Men
4 years ago
Supplements for losing toe nails?
I’m sure I’ve read that being Hashimotos can cause issues with nail plates / beds. Ever now and again I lose toe nails and have recently been hyper and lost another nail again. I also have skin growing over the sides of my nails which is annoying. Just wondering if anyone can recommend anything that
I’m sure I’ve read that being Hashimotos can cause issues with nail plates / beds. Ever now and again I lose toe nails and have recently been hyper and lost another nail again. I also have skin growing over the sides of my nails which is annoying. Just wondering if anyone can recommend anything that
MissFG
in
Thyroid UK
4 years ago
Self monitoring approaches: apps and strategies for high risk skin cancer
Hi there, i learned recently that I am at high risk of melanoma due to gene mutation so time to turn up the active monitoring strategies and so looking for info on which approaches work for people. So i see mobile apps that let you track and even a few that use machine learning to assess moles, i see
Hi there, i learned recently that I am at high risk of melanoma due to gene mutation so time to turn up the active monitoring strategies and so looking for info on which approaches work for people. So i see mobile apps that let you track and even a few that use machine learning to assess moles, i see
45RPM
in
Skin Cancer UK
4 years ago
Any particular concerns about having a boil on shoulder and primary lymphoedema affecting lower limbs?
Probably coincidence, but in 2016 I first developed lymphoedema symptoms in my right foot and leg. Shortly afterwards I had a very nasty boil on my shoulder which lasted several months but eventually (with help of antibiotics) get better but left a large scar. Now another boil has developed where
Probably coincidence, but in 2016 I first developed lymphoedema symptoms in my right foot and leg. Shortly afterwards I had a very nasty boil on my shoulder which lasted several months but eventually (with help of antibiotics) get better but left a large scar. Now another boil has developed where
DeborahS32
in
LSN
4 years ago
Update on diagnosis with ANA + symptoms only!
hi guys, i posted a week ago on here about how i was confused about my lupus diagnosis since my doctor diagnosed me on symptoms and positive ANA alone and started me on treatment right away. She did give me more blood tests, MRI, and ultrasound but she said even if those come back normal shed still
hi guys, i posted a week ago on here about how i was confused about my lupus diagnosis since my doctor diagnosed me on symptoms and positive ANA alone and started me on treatment right away. She did give me more blood tests, MRI, and ultrasound but she said even if those come back normal shed still
aimenkhattak27
in
LUPUS UK
4 years ago
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