Search
Search
About
Log in
Join
Experiences with
Hookworm infection
Read more...
Posts
Communities
28,488 public posts
Filter results
Allergic reaction To preventer inhaler
I have been on Symbicort pressurised inhaler for over 3 years but am Now getting side effects of pins & needles in my lips and fingers. I have eliminatedall my other medication and tried fostair and ellipta and they too are causing the same. Can anyone advise me of any other inhaler that does not contain
I have been on Symbicort pressurised inhaler for over 3 years but am Now getting side effects of pins & needles in my lips and fingers. I have eliminatedall my other medication and tried fostair and ellipta and they too are causing the same. Can anyone advise me of any other inhaler that does not contain
pam7974
in
Asthma Community Forum
5 months ago
Preventing COVID-19 & Other Respiratory Infections in Those with CLL / SLL During Peak Winter Months Tuesday, December 5, 2023 12:30 PM ET
Preventing COVID-19 and Other Respiratory Infections in Those with CLL / SLL During Peak Winter Months Tuesday, December 5, 2023 12:30 PM ET – 2 PM ET / 9:30 AM PT – 11 AM PT / 10:30 AM MT – 12 PM MT / 11:30 AM CT – 1 PM CT https://cllsociety.org/preventing-covid-19-and-other-respiratory-infections-in-those-with-cll-sll-during-peak-winter-months
Preventing COVID-19 and Other Respiratory Infections in Those with CLL / SLL During Peak Winter Months Tuesday, December 5, 2023 12:30 PM ET – 2 PM ET / 9:30 AM PT – 11 AM PT / 10:30 AM MT – 12 PM MT / 11:30 AM CT – 1 PM CT https://cllsociety.org/preventing-covid-19-and-other-respiratory-infections-in-those-with-cll-sll-during-peak-winter-months
lankisterguy
Volunteer
in
CLL Support
7 months ago
Pes Anserine Bursitis - steroid injection offered.
On Thursday I had an appointment with a rheumatologist who had previously been quite impatient and dismissive of me. I made up my mind to give him the briefest details of my woes over the last 9 months. (This is a 6 monthly appointment 😂). He was happy for me to continue with my slow tapering and then
On Thursday I had an appointment with a rheumatologist who had previously been quite impatient and dismissive of me. I made up my mind to give him the briefest details of my woes over the last 9 months. (This is a 6 monthly appointment 😂). He was happy for me to continue with my slow tapering and then
Sukydee
in
PMRGCAuk
2 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Covid and platelets
I’ve been on treatment for triple negative ET for almost three years now., taking Hydroxycarbomide (2 one day snd 3 the next) plus aspirin. Over the last year my platelets have come down to 540. However, since my last test three months ago, I have had Covid and a Covid vaccine. My blood test result
I’ve been on treatment for triple negative ET for almost three years now., taking Hydroxycarbomide (2 one day snd 3 the next) plus aspirin. Over the last year my platelets have come down to 540. However, since my last test three months ago, I have had Covid and a Covid vaccine. My blood test result
EdwinaJ
in
MPN Voice
7 months ago
New to PMR
Hi everyone -- I am new here and have had PMR for about five months now. I can't help wondering if the last Covid vaccine I received may have possibly triggered it, since my symptoms started less than a month after that. (I had already had five previous Covid vaccines.) I was also going through a period
Hi everyone -- I am new here and have had PMR for about five months now. I can't help wondering if the last Covid vaccine I received may have possibly triggered it, since my symptoms started less than a month after that. (I had already had five previous Covid vaccines.) I was also going through a period
Charlotteab
in
PMRGCAuk
7 months ago
I am nervous
Today was a rough day and I do t know what I am going to do in two weeks I’m so nervous. For the past month or so I have been getting injections done on my back it started out with steroid injections that didn’t work.. After a couple of them the Dr. switched them up and decided to do the arthritic
Today was a rough day and I do t know what I am going to do in two weeks I’m so nervous. For the past month or so I have been getting injections done on my back it started out with steroid injections that didn’t work.. After a couple of them the Dr. switched them up and decided to do the arthritic
Dolphfan47
in
Anxiety and Depression Support
2 months ago
managing anxiety
I’ve tested COVID positive. Feeling pretty crap but not as badly as the first couple times. Strangely no one else in the house has caught it. Just me. Initially I was feeling quite panicky about it but I’m managing pretty well. I just hope being quarantined won’t make me slip back into a place of comfort
I’ve tested COVID positive. Feeling pretty crap but not as badly as the first couple times. Strangely no one else in the house has caught it. Just me. Initially I was feeling quite panicky about it but I’m managing pretty well. I just hope being quarantined won’t make me slip back into a place of comfort
MindfulMoment
in
Anxiety and Depression Support
7 months ago
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
7 months ago
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
7 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
7 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
7 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
7 months ago
clinical trial vyd222 monoclonal AB against covid update science 37
thought i'd give an update on my experience with this study. i got my first infusion on oct 17th and had no ill effects other than my blood pressure getting super high. but i think that was from the last minute fumbles in planning thru science 37. my infusion medicine was supposed to arrive the afternoon
thought i'd give an update on my experience with this study. i got my first infusion on oct 17th and had no ill effects other than my blood pressure getting super high. but i think that was from the last minute fumbles in planning thru science 37. my infusion medicine was supposed to arrive the afternoon
bachplayer13
in
CLL Support
7 months ago
COVID-19 Infection effect on Urinary Incontinence and Mirabegron.
Dear Simon Foundation, I'm an old member of HU as a CLL type Leukaemia patient in the UK, but only just discovered your Simon foundation. Now I've always had poor bladder control and that could be due to bladder sensitivity, BPH, or damaged nerves in my lower back or all three, or more. I've gone through
Dear Simon Foundation, I'm an old member of HU as a CLL type Leukaemia patient in the UK, but only just discovered your Simon foundation. Now I've always had poor bladder control and that could be due to bladder sensitivity, BPH, or damaged nerves in my lower back or all three, or more. I've gone through
Ernest2
in
The Simon Foundation for Continence
7 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
6 months ago
What is classed as a flare?
Hi, I was diagnosed in November, had a steroid injection and started on MTX, once the steroid started wearing off the pain and swelling in my knees returned straight away but not in my hands, they have been great. Had a load of fluid sucked out of my knee and another steroid injection about 6 weeks ago
Hi, I was diagnosed in November, had a steroid injection and started on MTX, once the steroid started wearing off the pain and swelling in my knees returned straight away but not in my hands, they have been great. Had a load of fluid sucked out of my knee and another steroid injection about 6 weeks ago
Cat-E
in
NRAS
2 months ago
Covid vax and AFIB
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
just as an FYI, I had a Covid vaccination (Pfizer) a couple of days ago and I developed AFIB within a few hours. It did resolve itself overnight after I took extra metoprolol.
Awksom
in
CLL Support
7 months ago
Mumps contact 😷
Hi Peeps 🙂 I hope this post finds you as well as can be 🫠 I am writing to ask about contact with mumps. I have RA and my main meds are Tocilizumab (injection), Methotrexate (injection) and Sulphasalazine. Do I have to be particularly careful that I do not come in contact with a child who possibly has
Hi Peeps 🙂 I hope this post finds you as well as can be 🫠 I am writing to ask about contact with mumps. I have RA and my main meds are Tocilizumab (injection), Methotrexate (injection) and Sulphasalazine. Do I have to be particularly careful that I do not come in contact with a child who possibly has
Moomin8
in
NRAS
6 months ago
steroid injection in the joint
hi all It’s good to be back 😊I do look in here from time to time but have been too busy tone really active on the forum … I now have a quick query which I feel sure people on here can help me with. I have been referred to the MSK service for severe shoulder arthritis and they want to give me a steroid
hi all It’s good to be back 😊I do look in here from time to time but have been too busy tone really active on the forum … I now have a quick query which I feel sure people on here can help me with. I have been referred to the MSK service for severe shoulder arthritis and they want to give me a steroid
Nextoneplease
in
PMRGCAuk
2 months ago
pneumonia jab
hi , I’ve booked to have a jab privately as I wasn’t having any luck requesting it from the gp. Is this definitely safe for me to have with liver disease. Thanks
hi , I’ve booked to have a jab privately as I wasn’t having any luck requesting it from the gp. Is this definitely safe for me to have with liver disease. Thanks
Etymolog
in
British Liver Trust
6 months ago
1
...
28
29
30
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Lung Conditions Community Forum
2940 results
Fertility Network UK
2870 results
NRAS
2344 results
View top 10 communities
Sort by
Most Relevant
Newest