Search
Search
About
Log in
Join
Experiences with
Mouth, throat and dental infections
Posts
Communities
66,701 public posts
Filter results
Covid advice
Has anybody got any advice on how to deal with Covid when on combination therapy? I've just gone down with it for the first time and I'm wondering if I should just continue as normal. Have a pretty high fever and heart rate...wd the T3 exacerbate this?
Has anybody got any advice on how to deal with Covid when on combination therapy? I've just gone down with it for the first time and I'm wondering if I should just continue as normal. Have a pretty high fever and heart rate...wd the T3 exacerbate this?
SilverSavvy
in
Thyroid UK
9 months ago
Colds and flu…🧐🥹?
”Why don’t lupus patients catch cold? Many, many patients comment on this observation – that during cold and flu epidemics they seem to be the only family member not affected…?”
Professor Graham Hughes, [the London Lupus Centre] 2008
Just wondering about this observation but I personally have
”Why don’t lupus patients catch cold? Many, many patients comment on this observation – that during cold and flu epidemics they seem to be the only family member not affected…?”
Professor Graham Hughes, [the London Lupus Centre] 2008
Just wondering about this observation but I personally have
Suvi8901
in
LUPUS UK
9 months ago
Thyroid Ultrasound
Hi all, I have the results of my ultrasound and it says it's normal?! How can that be? Can the knowledgeable people on here help me to interpret the ultrasound report below. Her USS is normal done on 27th Jan US THYROID: The right lobe measures at the lower limit of normal 4.3 ml. The lobe is lobulated
Hi all, I have the results of my ultrasound and it says it's normal?! How can that be? Can the knowledgeable people on here help me to interpret the ultrasound report below. Her USS is normal done on 27th Jan US THYROID: The right lobe measures at the lower limit of normal 4.3 ml. The lobe is lobulated
Cassav
in
Thyroid UK
6 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
covid booster causing PMR flare?
I’d welcome any thoughts/advice please. Had covid booster, 4th, last Friday. Modena same as last year but under its new name, Spikway. Sore arm, very, very tired…done virtually nothing for last two and a half days. Yesterday and today all PMR pains very sore. Bilateral hips, shoulders, neck and biceps
I’d welcome any thoughts/advice please. Had covid booster, 4th, last Friday. Modena same as last year but under its new name, Spikway. Sore arm, very, very tired…done virtually nothing for last two and a half days. Yesterday and today all PMR pains very sore. Bilateral hips, shoulders, neck and biceps
Hulotsholiday
in
PMRGCAuk
9 months ago
Vitamin B1
I read that if you have RLS you might be short of vitamin B1. Has anyone knowledge of this.
I read that if you have RLS you might be short of vitamin B1. Has anyone knowledge of this.
Bridall
in
Restless Legs Syndrome
1 month ago
Finished Venetoclax, then Covid
My doctor prescribed Venetoclax after two rounds of chemo/immuno infusions to fight CLL. I felt great! Swimming half a mile, felt strong. Then bronchitis, pneumonia, and Covid. Was hospitalized and released in 6 days. But my home convalescence is not what I expected. Weakness, coughing, general severe
My doctor prescribed Venetoclax after two rounds of chemo/immuno infusions to fight CLL. I felt great! Swimming half a mile, felt strong. Then bronchitis, pneumonia, and Covid. Was hospitalized and released in 6 days. But my home convalescence is not what I expected. Weakness, coughing, general severe
Healmenow
in
CLL Support
8 months ago
well another drug fail.
Rituximab after 3 months is a failure. I have been so much worse the last 6 weeks unable to walk or use my hands peripheral neuropathy off the scale . Managed to see another rheumatologist at the clinic . 3 infections and bed bound these last 6 weeks. Given a steroid injection and will see me in 2 months
Rituximab after 3 months is a failure. I have been so much worse the last 6 weeks unable to walk or use my hands peripheral neuropathy off the scale . Managed to see another rheumatologist at the clinic . 3 infections and bed bound these last 6 weeks. Given a steroid injection and will see me in 2 months
J1707-
in
NRAS
9 months ago
Neutrophils
Hi everyone new here. I've just got my bloods back from gp and I have low white cell count (neutrophils) this leaves me open to infection as I'm sure your all aware that is a side effect of Roactemra. The consultant has now stopped my injection for 1 week and then repeat bloods in 4 weeks. My question
Hi everyone new here. I've just got my bloods back from gp and I have low white cell count (neutrophils) this leaves me open to infection as I'm sure your all aware that is a side effect of Roactemra. The consultant has now stopped my injection for 1 week and then repeat bloods in 4 weeks. My question
Headpain24
in
PMRGCAuk
2 months ago
IBS or something more?
Hi, this is my first post on here, and I'm just wondering if anyone can calm my anxiety and mind...For the past 4 years, I've had what I can only call unusual symptoms...bloating, passing a lot of blood from my back passage (clots included and the amount I'd pass during a heavy period), a lot of mucus
Hi, this is my first post on here, and I'm just wondering if anyone can calm my anxiety and mind...For the past 4 years, I've had what I can only call unusual symptoms...bloating, passing a lot of blood from my back passage (clots included and the amount I'd pass during a heavy period), a lot of mucus
SES05
in
IBS Network
2 months ago
How effective is fenofibrate for itch?
My doctor suggested a few different drugs, like rifampricin, naltrexone, and fenofibrate for my itch. He prescribed fenofibrate as he thinks it works best. Does anyone here take it and if so, has it helped? I'm worried about the warnings it comes with about severe liver damage.
My doctor suggested a few different drugs, like rifampricin, naltrexone, and fenofibrate for my itch. He prescribed fenofibrate as he thinks it works best. Does anyone here take it and if so, has it helped? I'm worried about the warnings it comes with about severe liver damage.
Carly92
in
PBC Foundation
8 months ago
Dry frizzy hair due to MBC medication,
I’ve been on Ibrance and Faslodex for 4-1/2 years. Although I’m thankful that the meds have helped me so far, I would like to know if anyone has found a good shampoo and conditioner to help with dry, straight and frizzy hair, My old shiny and wavy hair changed significantly since start of MBC drugs
I’ve been on Ibrance and Faslodex for 4-1/2 years. Although I’m thankful that the meds have helped me so far, I would like to know if anyone has found a good shampoo and conditioner to help with dry, straight and frizzy hair, My old shiny and wavy hair changed significantly since start of MBC drugs
mspti8383
in
SHARE Metastatic Breast Cancer
6 months ago
tinnitus after covid
Hi, Has anyone suffered tinnitus for a long time after covid or did it eventually go? If so, how long before it cleared up? Thanks
Hi, Has anyone suffered tinnitus for a long time after covid or did it eventually go? If so, how long before it cleared up? Thanks
Rabb5
in
Tinnitus UK
9 months ago
Isn’t this so true?
In today’s newspaper…….Not getting better During the pandemic, virtually every GP surgery in the land closed its doors as people were told to stay away from the NHS. The reason was purportedly to stop the hospitals overflowing but it effectively put the entire system out of reach for those who did not
In today’s newspaper…….Not getting better During the pandemic, virtually every GP surgery in the land closed its doors as people were told to stay away from the NHS. The reason was purportedly to stop the hospitals overflowing but it effectively put the entire system out of reach for those who did not
AgedCrone
in
NRAS
9 months ago
Covid and under active thyroid
I have just had covid for first time, and it hit me pretty badly, like a bad flu. My glands felt really swollen during it, particularly before, and still do. I'm also so tired. Sleeping a lot. Feel sluggish. Fat for no reason and constipated. This is all the feeling for me that my thyroid is under
I have just had covid for first time, and it hit me pretty badly, like a bad flu. My glands felt really swollen during it, particularly before, and still do. I'm also so tired. Sleeping a lot. Feel sluggish. Fat for no reason and constipated. This is all the feeling for me that my thyroid is under
Billy2023
in
Thyroid UK
9 months ago
Joint Steroid Injection
Hi,Im due to have a Steroid Injection in my knee to hopefully relieve the symptoms of Osteoarthritis. Which is very painful most of the time, and can be very debilitating. Just Wondering if anyone has had this done and knows how long it lasts before wearing off? Do they work? Are they worth having done
Hi,Im due to have a Steroid Injection in my knee to hopefully relieve the symptoms of Osteoarthritis. Which is very painful most of the time, and can be very debilitating. Just Wondering if anyone has had this done and knows how long it lasts before wearing off? Do they work? Are they worth having done
Tina1591
in
NRAS
9 months ago
After 2 Nuclear Ligand treatments should I still have severe bone pain in my lower back?
My SO was diagnosed last year with stage 4 Prostate cancer. Although his PSA never went extremely high (8.0) his Gleason scores were two 8's and a 9. The cancer when diagnosed consumed his complete prostate and was found in the vertebras of his neck, shoulder and shoulder socket plus his pelvis and
My SO was diagnosed last year with stage 4 Prostate cancer. Although his PSA never went extremely high (8.0) his Gleason scores were two 8's and a 9. The cancer when diagnosed consumed his complete prostate and was found in the vertebras of his neck, shoulder and shoulder socket plus his pelvis and
chuigk
in
Advanced Prostate Cancer
6 months ago
Dustasteride (avodart)
My doc has prescribed this drug for benign prostatic hyperplasia. I need help with urinary frequency, urgency, and frequent night time urination. It is too early to tell if the drug is helping. It can three to six months to have the desired effect of reducing prostate swelling. I am posting because
My doc has prescribed this drug for benign prostatic hyperplasia. I need help with urinary frequency, urgency, and frequent night time urination. It is too early to tell if the drug is helping. It can three to six months to have the desired effect of reducing prostate swelling. I am posting because
Parrsboro
in
Sensitive Issues for Men
6 months ago
The Origin of Ferritin Reference Intervals: A Systematic Review
I've slightly altered the formatting of the abstract in the hope of making it easier to read. ... Authors : Judy Truong, Kanza Naveed, Daniel Beriault, David Lightfoot, Michael Fralick, Michelle Sholzberg Link : https://ashpublications.org/blood/article/140/Supplement%201/11078/490505/The-Origin-of-Ferritin-Reference-Intervals-A
I've slightly altered the formatting of the abstract in the hope of making it easier to read. ... Authors : Judy Truong, Kanza Naveed, Daniel Beriault, David Lightfoot, Michael Fralick, Michelle Sholzberg Link : https://ashpublications.org/blood/article/140/Supplement%201/11078/490505/The-Origin-of-Ferritin-Reference-Intervals-A
humanbean
in
Thyroid UK
2 months ago
Bowel changes and pain. Positive faecal calprotectin, negative CT
Hello! I've had longstanding pelvic and back pain for some years now (gynaecology have been no help at all unfortunately) but since last October, my bowels have been affected (pain before and after going to the toilet, and alternating loose stools and constipation. I'm thinking there must be swelling
Hello! I've had longstanding pelvic and back pain for some years now (gynaecology have been no help at all unfortunately) but since last October, my bowels have been affected (pain before and after going to the toilet, and alternating loose stools and constipation. I'm thinking there must be swelling
Jennyjenjen01
in
Crohn's and Colitis Support
2 months ago
Mebeverine
Has anyone else found that their symptoms of IBS increase after taking mebervive. I was prescribed it, and when I have taken it my stomach flares up, I get major bloating and really sharp stomach pains? Has anyone else had this or is it just me?
Has anyone else found that their symptoms of IBS increase after taking mebervive. I was prescribed it, and when I have taken it my stomach flares up, I get major bloating and really sharp stomach pains? Has anyone else had this or is it just me?
Loveheartsx
in
IBS Network
2 months ago
1
...
96
97
98
...
100
Next page
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
5018 results
Advanced Prostate Cancer
3668 results
Lung Conditions Community Forum
3529 results
View top 10 communities
Sort by
Most Relevant
Newest