Search
Search
About
Log in
Join
Experiences with
Steroid injections
Posts
Communities
43,404 public posts
Filter results
Eliquis, covid, travel- not sure how to proceed
I was planning on starting Eliquis today (really I am supposed to start it on Tuesday but I will be traveling) but I think I have covid, (tested negative but it is abdominal/fever/hurty skin and similar symptoms to my last round of covid). I am due to fly long haul Tuesday and wanted to start the eliquis
I was planning on starting Eliquis today (really I am supposed to start it on Tuesday but I will be traveling) but I think I have covid, (tested negative but it is abdominal/fever/hurty skin and similar symptoms to my last round of covid). I am due to fly long haul Tuesday and wanted to start the eliquis
Iamfuzzyduck
in
Atrial Fibrillation Support
5 months ago
Why did we lose trust during the pandemic?
Why did we lose trust during the pandemic? My conversation with Kelley Krohnert KATELYN JETELINA MAR 14, 2024 “Your Local Epidemiologist (YLE)” https://yourlocalepidemiologist.substack.com/p/why-did-we-lose-trust-during-the I am very concerned about declining trust in science and public health.
Why did we lose trust during the pandemic? My conversation with Kelley Krohnert KATELYN JETELINA MAR 14, 2024 “Your Local Epidemiologist (YLE)” https://yourlocalepidemiologist.substack.com/p/why-did-we-lose-trust-during-the I am very concerned about declining trust in science and public health.
lankisterguy
Volunteer
in
CLL Support
5 months ago
Covid/ Covid vac / AF
hi all The more I look into my AF history from original GP appointment for breathlessness to now being on the Ablation waiting list I can’t help thinking there is a link I had Covid the early part of December 2021 a vaccine January 2022 by mid February I was seeing the GP about breathing difficulty
hi all The more I look into my AF history from original GP appointment for breathlessness to now being on the Ablation waiting list I can’t help thinking there is a link I had Covid the early part of December 2021 a vaccine January 2022 by mid February I was seeing the GP about breathing difficulty
NLGA
in
Atrial Fibrillation Support
5 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
cramp like pain at night from left buttock right down leg
I posted a similar issue not so long ago as a sort of 3am phenomenon. Lately it has got worse and I thought maybe I was tapering pred too quickly ( down to 6/7 mg.) So have taken 10 mg for 2 days and am ok in the day but am now up at5.30 am having experienced first quite severe cramp in my lower left
I posted a similar issue not so long ago as a sort of 3am phenomenon. Lately it has got worse and I thought maybe I was tapering pred too quickly ( down to 6/7 mg.) So have taken 10 mg for 2 days and am ok in the day but am now up at5.30 am having experienced first quite severe cramp in my lower left
Stargiver
in
PMRGCAuk
10 months ago
New here
Hi everyone. I’m new here. 32 weeks pregnant and experiencing severe urethral pain for over a month. Doctors think the baby is on the nerves supplying the urethra. Cystoscopy was clear, no uti. Has anyone ever had this experience? Constant urge to pee and lightning bolts every few minutes shooting down
Hi everyone. I’m new here. 32 weeks pregnant and experiencing severe urethral pain for over a month. Doctors think the baby is on the nerves supplying the urethra. Cystoscopy was clear, no uti. Has anyone ever had this experience? Constant urge to pee and lightning bolts every few minutes shooting down
PrincessPeachPirate
in
Pelvic Pain Support Network
5 months ago
How can I reduce the swelling in my foot and ankle?
Hello I was diagnosed with RA about six weeks ago and am on 20 mg methotrexate and 5 mg folic acid and have had a steroid injection. I can see improvement in other places but my right foot and ankle are swollen so I can only walk really short distances with a limp. I am worried that I will not be able
Hello I was diagnosed with RA about six weeks ago and am on 20 mg methotrexate and 5 mg folic acid and have had a steroid injection. I can see improvement in other places but my right foot and ankle are swollen so I can only walk really short distances with a limp. I am worried that I will not be able
spartacus101
in
NRAS
1 year ago
Possible Kidney Failure
Hello: My husband had a liver transplant many years ago and has done very well, for which we are very grateful. Since October of 2023, his creatinine started rising and his egfr started falling. He had blood work done several times since then. He latest egfr is 45, his creatinine is 1.6 and his BUN
Hello: My husband had a liver transplant many years ago and has done very well, for which we are very grateful. Since October of 2023, his creatinine started rising and his egfr started falling. He had blood work done several times since then. He latest egfr is 45, his creatinine is 1.6 and his BUN
PennyLovas
in
Kidney Disease
7 months ago
Covid vaccines cut risk of virus-related heart failure and blood clots, study finds
Covid vaccines cut risk of virus-related heart failure and blood clots, study finds https://www.theguardian.com/science/2024/mar/12/covid-vaccines-cut-risk-virus-related-heart-failure-blood-clots-study Researchers say jabs substantially reduce for up to a year the chances of serious cardiovascular complications
Covid vaccines cut risk of virus-related heart failure and blood clots, study finds https://www.theguardian.com/science/2024/mar/12/covid-vaccines-cut-risk-virus-related-heart-failure-blood-clots-study Researchers say jabs substantially reduce for up to a year the chances of serious cardiovascular complications
lankisterguy
Volunteer
in
CLL Support
5 months ago
Is it tapering or adrenals?
I'm in hols at the moment, so probably have doing a bit too much! However, today I have shortness of breath doing the slightest thing, even sitting down, and feeling faint and wobbly. I'm a bit better now I've rested all day.Do you think I just need to up my steroids for a couple of days(I've been
I'm in hols at the moment, so probably have doing a bit too much! However, today I have shortness of breath doing the slightest thing, even sitting down, and feeling faint and wobbly. I'm a bit better now I've rested all day.Do you think I just need to up my steroids for a couple of days(I've been
CoziNess
in
PMRGCAuk
10 months ago
Sleep aids
Hoping that people can pass on what they use to help sleep with T. Realise there are likely to be a number of replies through various posts, but be good to hear what works for people on this thread if possible. ..on another note are steroids likely to spike tinnitus? Just finishing a 5 day course prescribed
Hoping that people can pass on what they use to help sleep with T. Realise there are likely to be a number of replies through various posts, but be good to hear what works for people on this thread if possible. ..on another note are steroids likely to spike tinnitus? Just finishing a 5 day course prescribed
Cityfan1
in
Tinnitus UK
10 months ago
cataracts b.c. of long-term steroids
Does anyone know what the symptoms of cataracts developing are, after long-term use of inhaled steroids and/or prednisolone? I've heard cataracts are common symptoms, and I wonder how one knows one is developing them. I've been on Trimbow 172.5 for 6 months and on 2 mg prednisone for 2.5 years; prior
Does anyone know what the symptoms of cataracts developing are, after long-term use of inhaled steroids and/or prednisolone? I've heard cataracts are common symptoms, and I wonder how one knows one is developing them. I've been on Trimbow 172.5 for 6 months and on 2 mg prednisone for 2.5 years; prior
runcyclexcski
in
Asthma Community Forum
10 months ago
Buprenorphine
Hello, have many UK people found it easy or hard to get Buprenorphine px by GP to control pain from RLS? I have been withdrawing from Pramepexole and using only codeine however it is now not effective in controlling my pain. I have a GP appointment in a few days and was going to ask for Buprenorphine
Hello, have many UK people found it easy or hard to get Buprenorphine px by GP to control pain from RLS? I have been withdrawing from Pramepexole and using only codeine however it is now not effective in controlling my pain. I have a GP appointment in a few days and was going to ask for Buprenorphine
Cookiebum24
in
Restless Legs Syndrome
4 months ago
covid and metratrexate
Hi all!! So I have RA and I’m taking metratrexate so around 3 wks ago I had covid and have to stop the metratrexate and steroid tablets that had just been prescribed!.so I was told I couldn’t take my metratrexate or steroid pills until my covid test is negative as yesterday still showing positive
Hi all!! So I have RA and I’m taking metratrexate so around 3 wks ago I had covid and have to stop the metratrexate and steroid tablets that had just been prescribed!.so I was told I couldn’t take my metratrexate or steroid pills until my covid test is negative as yesterday still showing positive
Mybirthday1975
in
FieryBones - RA Community
5 months ago
covid and metratrexate
Hi all!! So I have RA and I’m taking metratrexate so around 3 wks ago I had covid and have to stop the metratrexate and steroid tablets that had just been prescribed!.so I was told I couldn’t take my metratrexate or steroid pills until my covid test is negative as yesterday still showing positive although
Hi all!! So I have RA and I’m taking metratrexate so around 3 wks ago I had covid and have to stop the metratrexate and steroid tablets that had just been prescribed!.so I was told I couldn’t take my metratrexate or steroid pills until my covid test is negative as yesterday still showing positive although
Mybirthday1975
in
NRAS
5 months ago
Itchy skin
Hi I have suffered with poly myalgia for about four years. Having been prescribed predisalone 20mg daily the pains went away and I am on a very very slow reduction, now only 1.5 mg daily. Six months ago I started with patches of itchy skin, sides of hands, hairline and round my eyes. GP thought it
Hi I have suffered with poly myalgia for about four years. Having been prescribed predisalone 20mg daily the pains went away and I am on a very very slow reduction, now only 1.5 mg daily. Six months ago I started with patches of itchy skin, sides of hands, hairline and round my eyes. GP thought it
CathieT
in
PMRGCAuk
7 months ago
Solving the puzzle of Long Covid
Published 22 Feb 2024. Long COVID is finally getting some attention. Not pay-walled. https://www.science.org/doi/10.1126/science.adl0867
Published 22 Feb 2024. Long COVID is finally getting some attention. Not pay-walled. https://www.science.org/doi/10.1126/science.adl0867
zaax
in
CLL Support
5 months ago
dipyridamole
I’m going to try this next week when I get an Rx. Looking for any pointers from anyone who has had success with it. I gather that 225mg is a common dose for RLS (three 75mg pills). I intend to start with one pill and titrate up to three quickly if there are no issues. I’m currently using buprenorphine
I’m going to try this next week when I get an Rx. Looking for any pointers from anyone who has had success with it. I gather that 225mg is a common dose for RLS (three 75mg pills). I intend to start with one pill and titrate up to three quickly if there are no issues. I’m currently using buprenorphine
707twitcher
in
Restless Legs Syndrome
4 months ago
Immunology when using donor eggs
Hello Hope everyone is doing as well as they can be Sorry to be writing again. I don't really know where else to ask these kind of questions. We have looked into donor egg treatment both in UK and abroad and have had a few consultations. But remain undecided on the clinic and I don't know if that's
Hello Hope everyone is doing as well as they can be Sorry to be writing again. I don't really know where else to ask these kind of questions. We have looked into donor egg treatment both in UK and abroad and have had a few consultations. But remain undecided on the clinic and I don't know if that's
Skittles11
in
Fertility Network UK
10 months ago
Pegasys is applying for formal approval in MPN treatment
Dear friends, I came across a EMA document recently and found that Pegasys is applying for indication extension to PV and ET. It provides, on page 53: “Grouped application consisting of: Extension of indication to include treatment of Polycythaemia Vera (PV) and Essential thrombocytopenia (ET) for
Dear friends, I came across a EMA document recently and found that Pegasys is applying for indication extension to PV and ET. It provides, on page 53: “Grouped application consisting of: Extension of indication to include treatment of Polycythaemia Vera (PV) and Essential thrombocytopenia (ET) for
TimothyHLuff
in
MPN Voice
8 months ago
Questions about TSH and advice on results over the past year much appreciated
Hi everybody, I've posted several times lately and I just wanted to ask for advice on thyroid related issues. I had COVID 3 times from June 22 - Jan 23 and was symptomatic each time. I did have a diagnosis of Fibromyalgia in 2018 but had been feeling a lot better in 2020 until I got COVID. Above
Hi everybody, I've posted several times lately and I just wanted to ask for advice on thyroid related issues. I had COVID 3 times from June 22 - Jan 23 and was symptomatic each time. I did have a diagnosis of Fibromyalgia in 2018 but had been feeling a lot better in 2020 until I got COVID. Above
Heybella
in
Thyroid UK
5 months ago
1
...
76
77
78
...
100
Next page
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
PMRGCAuk
4819 results
Lung Conditions Community Forum
4417 results
Asthma Community Forum
3815 results
View top 10 communities
Sort by
Most Relevant
Newest