Search
Search
About
Log in
Join
Experiences with
Gold thioglucose
Posts
Communities
202 public posts
Filter results
Very painful steroid injection
Hello! I wanted some advice or to hear there’s light at the end of this miserable tunnel I have been getting steroid injections for the last 10 years into my toes and my thumbs. I have just had to move house and the packing put my hands into a lot of pain. So the doctor put steroids into my thumbs and
Hello! I wanted some advice or to hear there’s light at the end of this miserable tunnel I have been getting steroid injections for the last 10 years into my toes and my thumbs. I have just had to move house and the packing put my hands into a lot of pain. So the doctor put steroids into my thumbs and
Tonkie
in
NRAS
17 days ago
Teeth!
Hi, Can anyone clarify please how Hashimotos affects teeth/gums? Or is it the Levothyroxine that does it? Whenever I mention to dentist, she is oblivious to this/never heard of it.My teeth have always suffered. Countless fillings, extractions, sensitivity, poor enamel, teeth practically disappearing!
Hi, Can anyone clarify please how Hashimotos affects teeth/gums? Or is it the Levothyroxine that does it? Whenever I mention to dentist, she is oblivious to this/never heard of it.My teeth have always suffered. Countless fillings, extractions, sensitivity, poor enamel, teeth practically disappearing!
MissDemeanour191
in
Thyroid UK
22 days ago
Bad cold sore should I wait to inject Methotrexate?
I was at the dentist last Thursday - not my usual one - and she was a bit rough! She split my lip in the corner and it's came out with large cold sores which are not healing! 😔 I'm considering not injecting today to give them a better chance to heal - what do you think? They're sore and I can't eat
I was at the dentist last Thursday - not my usual one - and she was a bit rough! She split my lip in the corner and it's came out with large cold sores which are not healing! 😔 I'm considering not injecting today to give them a better chance to heal - what do you think? They're sore and I can't eat
marie66
in
NRAS
6 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Cold & sore throat PAF
hi, I’ve had a cold and cough for 7 days now and having been having AF episodes lasting from 30mins - 5hours almost daily. Normally I would get an episode once a month at worst. Can colds and coughs bring on more regular occurances of AF?
hi, I’ve had a cold and cough for 7 days now and having been having AF episodes lasting from 30mins - 5hours almost daily. Normally I would get an episode once a month at worst. Can colds and coughs bring on more regular occurances of AF?
tom0985
in
Atrial Fibrillation Support
6 months ago
colds and coughs
I am recently diagnosed with RA, I am on immune blockers. And I keep getting colds and coughs. is this due to my immune system being reduced. And is there anything I can do to treat this? Thank you.
I am recently diagnosed with RA, I am on immune blockers. And I keep getting colds and coughs. is this due to my immune system being reduced. And is there anything I can do to treat this? Thank you.
Toiletseat
in
NRAS
6 months ago
Tips for knee pain at 68
Hi everyone, I'm Lyndon. I Woke up Saturday morning with a horrible surprise - knee pain. It's centered on the front left side of my right knee, a dull ache that's been keeping me up at night and making it tough to move around. At 68, I've had my fair share of aches and pains, but this is new territory
Hi everyone, I'm Lyndon. I Woke up Saturday morning with a horrible surprise - knee pain. It's centered on the front left side of my right knee, a dull ache that's been keeping me up at night and making it tough to move around. At 68, I've had my fair share of aches and pains, but this is new territory
LyndonH
in
Pain Concern
6 months ago
Cold sores
Hi looking for ABIT advice, my partner was diagnosed with CLL in 2016 he finished O&V treatment 2022 and all has been well with now 6 monthly review with his consultant. he's recently started to suffer from recurring coldsores and some joint pain that don't seem to be healing, he has no other previous
Hi looking for ABIT advice, my partner was diagnosed with CLL in 2016 he finished O&V treatment 2022 and all has been well with now 6 monthly review with his consultant. he's recently started to suffer from recurring coldsores and some joint pain that don't seem to be healing, he has no other previous
Hd07
in
CLL Support
8 months ago
still here
Hi All I like to try and update my journey so you can see that there are some longer term survivors. I am still on 0 PSA with advanced cancer. My journey is on my bio. I was diagnosed at 47 and now I’m 54 with no progression. My primary treatment was Zytiga and it is still working. I take a concoction
Hi All I like to try and update my journey so you can see that there are some longer term survivors. I am still on 0 PSA with advanced cancer. My journey is on my bio. I was diagnosed at 47 and now I’m 54 with no progression. My primary treatment was Zytiga and it is still working. I take a concoction
Apollo123
in
Advanced Prostate Cancer
9 months ago
Cold is good for you
Radio 4 currently has a series by Dr Michael Mosley, Cold Therapy. The third episode deals with exercising in the cold. One of his conclusions is that people who run reasonable distances for fun (as opposed to marathons, ultra runners, professionals) have their best performance at around 10-11C. Well
Radio 4 currently has a series by Dr Michael Mosley, Cold Therapy. The third episode deals with exercising in the cold. One of his conclusions is that people who run reasonable distances for fun (as opposed to marathons, ultra runners, professionals) have their best performance at around 10-11C. Well
Yesletsgo
Graduate10
in
Bridge to 10K
9 months ago
Colds/flu/viruses and Thyroxine
Just wondering is there any link to having Hashimotos and not having any colds/flu/viruses. The reason I ask is that I never got sick, with the usual colds etc for many years. I just started thyroxine a few months ago. Now I have a really horrible virus, coughing, temperature, flu like symptoms. This
Just wondering is there any link to having Hashimotos and not having any colds/flu/viruses. The reason I ask is that I never got sick, with the usual colds etc for many years. I just started thyroxine a few months ago. Now I have a really horrible virus, coughing, temperature, flu like symptoms. This
Sunflower535
in
Thyroid UK
1 year ago
Filgotinib with Colds Sore throat
Hello Can I ask I anyone on filgotinib, if you get cold (which feels like it's a head cold all stuffed up) and sore throat, do you stop filgotinib till its better or keep taking it? I know I have to stop if needing antibiotics but wasn't sure for a cold. Your experiences would be very welcome Thank
Hello Can I ask I anyone on filgotinib, if you get cold (which feels like it's a head cold all stuffed up) and sore throat, do you stop filgotinib till its better or keep taking it? I know I have to stop if needing antibiotics but wasn't sure for a cold. Your experiences would be very welcome Thank
EarthRock
in
NRAS
1 year ago
Restless legs
Morning hun. Iv had it for around 20 years iv always managed okBut Last Tuesday it started really bad and its day and night. Drs have given me some tablets for Parkinson they ste Not working. I'm just in the lounge walking all night 1-3 ,hour sleep a night Went to hospital Saturday they done bloods
Morning hun. Iv had it for around 20 years iv always managed okBut Last Tuesday it started really bad and its day and night. Drs have given me some tablets for Parkinson they ste Not working. I'm just in the lounge walking all night 1-3 ,hour sleep a night Went to hospital Saturday they done bloods
Frenhies
in
Restless Legs Syndrome
1 year ago
Problem with EBV
Hi all I have active EBV, but I can't take Lysine because it reduces my sleep-5,6 hours and I sleep very poorly by waking up several times during the night. My question is, is there anything else that can successfully replace Lysine. I've tried taking Valtrex, but I'm even worse off it, because it's
Hi all I have active EBV, but I can't take Lysine because it reduces my sleep-5,6 hours and I sleep very poorly by waking up several times during the night. My question is, is there anything else that can successfully replace Lysine. I've tried taking Valtrex, but I'm even worse off it, because it's
Stongwave
in
Thyroid UK
1 year ago
Right eye injury
I got hit in right eye upper region, after several hours swelling occurred, at time of injury and after 24 hours at time of diagnosis my vision was 6/6, severe pain and conjunctivitis was present, doctor subscribe me cold therapy and antibiotic, light sensitivity was present for 2 weeks, Vision is
I got hit in right eye upper region, after several hours swelling occurred, at time of injury and after 24 hours at time of diagnosis my vision was 6/6, severe pain and conjunctivitis was present, doctor subscribe me cold therapy and antibiotic, light sensitivity was present for 2 weeks, Vision is
Ravish340
in
Glaucoma UK
1 year ago
colds and flu
I’ve been Googling but can’t any answers. Is there a link between catching frequent colds and hashimotos?
I’ve been Googling but can’t any answers. Is there a link between catching frequent colds and hashimotos?
Reneey2k
in
Thyroid UK
1 year ago
Nail changes? Pale nails.
Hi, I have Hashimoto's and for the last few years, I've slightly overmedicated with levothyroxine though my endo was happy to do so, as I felt better. I noticed recently that I have what looks like the start of Terry's nails - pale (pale not completely white) nail beds with a dark pink line before
Hi, I have Hashimoto's and for the last few years, I've slightly overmedicated with levothyroxine though my endo was happy to do so, as I felt better. I noticed recently that I have what looks like the start of Terry's nails - pale (pale not completely white) nail beds with a dark pink line before
JackiePotatoes
in
Thyroid UK
1 year ago
My hands ..
So, my hands have been painful for a while now, my GP didn't seem to think they were bad and I was just told use hot/cold therapy ibuprofen gel.I have a very pronounced swollen index top joint the rest are just painful as the time and I'm really struggling with working as I'm IT based, I have a vertical
So, my hands have been painful for a while now, my GP didn't seem to think they were bad and I was just told use hot/cold therapy ibuprofen gel.I have a very pronounced swollen index top joint the rest are just painful as the time and I'm really struggling with working as I'm IT based, I have a vertical
Diamond61
in
NRAS
2 years ago
endometriosis and colds/flu
hi, does anyone else feel like having endometriosis makes things like colds and flu worse?? I’m sure I read somewhere that endometriosis can affect the immune system, think it’s linked with leaky gut. I seem to get colds a lot and when I do, they completely wipe me out, and they tend to flare up my endometriosis
hi, does anyone else feel like having endometriosis makes things like colds and flu worse?? I’m sure I read somewhere that endometriosis can affect the immune system, think it’s linked with leaky gut. I seem to get colds a lot and when I do, they completely wipe me out, and they tend to flare up my endometriosis
MayM95
in
Endometriosis UK
2 years ago
Cold Therapy After Heart Attack?
Hi, I used to enjoy cold showers twice a day and also after excercise before the heart attack exactly 16 weeks ago, 4 emergency stents inserted and the pile of meds each day I'm now feeling good but was wondering if anyone takes cold showers/ cold therapy after heart attack? thanks
Hi, I used to enjoy cold showers twice a day and also after excercise before the heart attack exactly 16 weeks ago, 4 emergency stents inserted and the pile of meds each day I'm now feeling good but was wondering if anyone takes cold showers/ cold therapy after heart attack? thanks
Blindheart
in
British Heart Foundation
2 years ago
mouth sores
Hi all Just a quick question about mouth sores which, are apparently a feature of lupus. I have had these intermittently on the roof of my mouth for as long as I can remember. I always assumed it was cold sores which I very occasionally get on my lip. But now I'm not sure. They first come up as
Hi all Just a quick question about mouth sores which, are apparently a feature of lupus. I have had these intermittently on the roof of my mouth for as long as I can remember. I always assumed it was cold sores which I very occasionally get on my lip. But now I'm not sure. They first come up as
Brychni
in
LUPUS UK
2 years ago
1
2
...
11
Next page
10
Filter results
Clear filters
Posted in
All communities
NRAS
30 results
Asthma Community Forum
28 results
Thyroid UK
23 results
View top 10 communities
Sort by
Most Relevant
Newest