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Thrush 3 days before FET
Hi everyone, I am booked for a natural FET on Monday (I didn't take anything this cycle, not even progesterone) and the Friday before I discovered that my discharge looked like cottage cheese and I may be getting thrush. Which I haven't had in years! Has this happened to anyone else before their FET
Hi everyone, I am booked for a natural FET on Monday (I didn't take anything this cycle, not even progesterone) and the Friday before I discovered that my discharge looked like cottage cheese and I may be getting thrush. Which I haven't had in years! Has this happened to anyone else before their FET
raverg
in
Fertility Network UK
4 months ago
Christmas Covid
Looks like our Christmas present was Covid. At my partners mothers and both tested positive one this morning and the others last Thursday but so far I’m negative but sure I’ll get it. not sure where we picked it up as been careful. I’m not sure what to do meds wise as I took my 15mg of MTX yesterday
Looks like our Christmas present was Covid. At my partners mothers and both tested positive one this morning and the others last Thursday but so far I’m negative but sure I’ll get it. not sure where we picked it up as been careful. I’m not sure what to do meds wise as I took my 15mg of MTX yesterday
Alan7690
in
NRAS
5 months ago
Steroids after 6 weeks
My Dr just called as he called the ENT and he said he will prescribe steroids whilst I'm waiting months for an appointment for acoustic shock/traum 6 weeks 2 days ago 60 my high dose at first then qill be reduced The Dr said a bit late but worth a try Is it worth it? I really don't like medication
My Dr just called as he called the ENT and he said he will prescribe steroids whilst I'm waiting months for an appointment for acoustic shock/traum 6 weeks 2 days ago 60 my high dose at first then qill be reduced The Dr said a bit late but worth a try Is it worth it? I really don't like medication
Laura878787
in
Tinnitus UK
10 months ago
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My Christmas
I did not attend the family gathering unfortunately since I have anxiety inside indoor spaces with groups of people, and we have COVID and flu going around. My concern with COVID is that some people get long term symptoms like chronic fatigue, loss of smell or taste, and a few others. So it just still
I did not attend the family gathering unfortunately since I have anxiety inside indoor spaces with groups of people, and we have COVID and flu going around. My concern with COVID is that some people get long term symptoms like chronic fatigue, loss of smell or taste, and a few others. So it just still
davidthecoder
in
Anxiety and Depression Support
5 months ago
Waking from sleep with upper abdominal pain for hours at a time
Does anyone have experience of this? Any advice very welcome. I wake from sleep with a slight discomfort, it builds and builds until I have to stand up very straight just to get a tiny bit of relief. Crouching and slow shuffling around also helps very slightly but sitting or lying down is excruciating
Does anyone have experience of this? Any advice very welcome. I wake from sleep with a slight discomfort, it builds and builds until I have to stand up very straight just to get a tiny bit of relief. Crouching and slow shuffling around also helps very slightly but sitting or lying down is excruciating
Jeromekjerome
in
Acid Reflux Support
10 months ago
Covid update
I had a call back after 2.5 days from the covid medication delivery unit. They asked me to go to the local hospital to get an infusion of sotrovimab. The tablets form interacts with some of my medication so this one was chosen. I will let you know how I do on it.
I had a call back after 2.5 days from the covid medication delivery unit. They asked me to go to the local hospital to get an infusion of sotrovimab. The tablets form interacts with some of my medication so this one was chosen. I will let you know how I do on it.
artydutch
in
MPN Voice
5 months ago
Check your Thyroid
For about a year I’ve been struggling. Fatigue getting worse, frozen shoulder, dry mouth and eyes, aching, brain fog, palpitations. It really got worse after last years autumn Covid booster when I thought I was having a heart attack. Heart all checked out fine. So I talked to my consultant at my clinic
For about a year I’ve been struggling. Fatigue getting worse, frozen shoulder, dry mouth and eyes, aching, brain fog, palpitations. It really got worse after last years autumn Covid booster when I thought I was having a heart attack. Heart all checked out fine. So I talked to my consultant at my clinic
Readlots
in
British Liver Trust
8 months ago
Laxido longterm use
Hi all,I've been taking 1,sometimes 2 laxido sachets daily for the past 3 months and this has helped.My gastroenteritis has suggested swapping for prucalopride 1mg but this gives me all day stomach ache.My question is,is laxido safe to use daily long term?
Hi all,I've been taking 1,sometimes 2 laxido sachets daily for the past 3 months and this has helped.My gastroenteritis has suggested swapping for prucalopride 1mg but this gives me all day stomach ache.My question is,is laxido safe to use daily long term?
Ladydaff1
in
IBS Network
8 months ago
autoimmunity
I went to Laurie Mischley’s alumni camp in August. One of the Labs that I decided to get done called Nuro zoomer I believe, had an interesting result. Turns out I have auto immunity to my glycine receptors. There’s not a whole lot about this online, but apparently in some cases it can cause parkinsonism
I went to Laurie Mischley’s alumni camp in August. One of the Labs that I decided to get done called Nuro zoomer I believe, had an interesting result. Turns out I have auto immunity to my glycine receptors. There’s not a whole lot about this online, but apparently in some cases it can cause parkinsonism
rebtar
in
Cure Parkinson's
8 months ago
Covid
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
hi all, I have been diagnosed with tumid lupus and am currently being investigated for SLE (DR said 99.9% I have it as showing all symptoms etc). I have just tested positive for covid today. Has anyone got any advise? I’ve never had covid, let alone Covid with lupus and I’m terrified this is going
JLAR01
in
LUPUS UK
5 months ago
Lilydunn
Tapering Issues.I am having problems when I taper below 3mgs. Dropped from 3 mgs to 2.5 over a 3 month taper.( This is 2nd attempt) Thought I was winning but caught a nasty cold virus and kept going thinking I could cope. Also had bereavement of best friend which hit hard. Have now crashed with aching
Tapering Issues.I am having problems when I taper below 3mgs. Dropped from 3 mgs to 2.5 over a 3 month taper.( This is 2nd attempt) Thought I was winning but caught a nasty cold virus and kept going thinking I could cope. Also had bereavement of best friend which hit hard. Have now crashed with aching
lilydunn
in
PMRGCAuk
10 months ago
Atorvastatin
Ive found that taken at night my dose causes morning headaches which are not alchol related!! Taken in the morning with other meds causes no adverse effects, well at least nothing noticable. I also take steroids & inhaler for copd and Amlodipine for raised BP along with Omeprazole for gut protection
Ive found that taken at night my dose causes morning headaches which are not alchol related!! Taken in the morning with other meds causes no adverse effects, well at least nothing noticable. I also take steroids & inhaler for copd and Amlodipine for raised BP along with Omeprazole for gut protection
Icom705
in
Cholesterol Support
10 months ago
Side effects of Buprenorphine
Several persons on this site have already helped me but I want to ask the general following about the use of Buprenorphine for treatment of RLS. and its augmentation After testing in vain, pregabalin, oxycodone several other less well advertised RLS treatments I got agreement from my GP to try Buprenorphine
Several persons on this site have already helped me but I want to ask the general following about the use of Buprenorphine for treatment of RLS. and its augmentation After testing in vain, pregabalin, oxycodone several other less well advertised RLS treatments I got agreement from my GP to try Buprenorphine
davchar23
in
Restless Legs Syndrome
4 months ago
Covid
I should have been at a relatives tonight but they phoned to say they’d got covid but thought I’d be ok to visit if I wore a mask. I said I wouldn’t be going, they think I’m being over cautious as “it’s just a cold these days”. I’m on Rux which I’ve been told will make me susceptible to infections.
I should have been at a relatives tonight but they phoned to say they’d got covid but thought I’d be ok to visit if I wore a mask. I said I wouldn’t be going, they think I’m being over cautious as “it’s just a cold these days”. I’m on Rux which I’ve been told will make me susceptible to infections.
lizzziep
in
MPN Voice
5 months ago
ANyone taking Prolia for osteoporosis?
Hi! I have been dealing with osteoporosis for more than 20 years and taken all the pills and Forteo shots. I have Lupus, Hyperparathyroidisn, Low Vitamin D and low body mass that all contribute to the problem. Unfortunately, it has continues to get worse. I have been hesitant to take Prolia as it will
Hi! I have been dealing with osteoporosis for more than 20 years and taken all the pills and Forteo shots. I have Lupus, Hyperparathyroidisn, Low Vitamin D and low body mass that all contribute to the problem. Unfortunately, it has continues to get worse. I have been hesitant to take Prolia as it will
Pumpkin2009
in
LUPUS UK
8 months ago
Post COVID UC flare - Mezavant probs
Hi I'm new, feeling a bit scared as it's Christmas time and my gastro not back til 8 January. I had COVID mid November, very nauseous and some diahhrea and very soft sticky stool. Mild proctosigmoiditis (low down UC) for 30 years. Been off meds for 20 years until now. Following COVID my bowel symptoms
Hi I'm new, feeling a bit scared as it's Christmas time and my gastro not back til 8 January. I had COVID mid November, very nauseous and some diahhrea and very soft sticky stool. Mild proctosigmoiditis (low down UC) for 30 years. Been off meds for 20 years until now. Following COVID my bowel symptoms
Bunnygirl1
in
Crohn's and Colitis Support
5 months ago
single mom w/adhd of 8yo w/adhd aaahhhhh
life was fine, my normal levels of crazy functioning till covid trashed it. her first 5years were just the 2 of us traveling the usa with ren fairs. since covid messed up my working with my kid. i've yet to get re-set. we've bounced around in our living environments, rented rooms in friends houses
life was fine, my normal levels of crazy functioning till covid trashed it. her first 5years were just the 2 of us traveling the usa with ren fairs. since covid messed up my working with my kid. i've yet to get re-set. we've bounced around in our living environments, rented rooms in friends houses
TCtallchick
in
CHADD's ADHD Parents Together
5 months ago
Another round of departments
I've joined several boards on here: initially PMR because that's what was diagnosed first, then the Lung board because after I saw the rheumatologist in January this year for the first time he said he'd like to try me on methotrexate but wanted a clear chest x-ray first - and that's when the fun really
I've joined several boards on here: initially PMR because that's what was diagnosed first, then the Lung board because after I saw the rheumatologist in January this year for the first time he said he'd like to try me on methotrexate but wanted a clear chest x-ray first - and that's when the fun really
ladygigger
in
PMRGCAuk
10 months ago
Synacthen Test Results
Hi everyone, just looking for some clarification on a Synacthen test I've had. Bit of background, 36M, pretty healthy in terms of diet, exercise, sleep etc. No medications. I've been suffering for a few months with fatigue, heart palpitations. Seems to get a lot worse after exercise. Checked cortisol
Hi everyone, just looking for some clarification on a Synacthen test I've had. Bit of background, 36M, pretty healthy in terms of diet, exercise, sleep etc. No medications. I've been suffering for a few months with fatigue, heart palpitations. Seems to get a lot worse after exercise. Checked cortisol
Lalalala5
in
Thyroid UK
10 months ago
Shingles Vaccination
Hi folks, just been sent a link for the Shingles Vaccine, is this something anyone else has had. I wasn't aware that when taking Methotrexate this was possible. Unfortunately I can never get through to my surgery to ask the question. Thank you
Hi folks, just been sent a link for the Shingles Vaccine, is this something anyone else has had. I wasn't aware that when taking Methotrexate this was possible. Unfortunately I can never get through to my surgery to ask the question. Thank you
Ports
in
NRAS
8 months ago
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