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tips on covid and newborn
so i found out i have Covid day after my son was born. I v been so scared to pass it on to him, iv been sleeping in a different room and cleaning up and washing real well before breastfeeding. With all the postpartum pain Covid symptoms and lack of sleep is making everything harder. Anyone been in a
so i found out i have Covid day after my son was born. I v been so scared to pass it on to him, iv been sleeping in a different room and cleaning up and washing real well before breastfeeding. With all the postpartum pain Covid symptoms and lack of sleep is making everything harder. Anyone been in a
Chantysal
in
Pregnancy and Parenting Support
8 months ago
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
Very interesting article: [u]
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
[/u]
2024
https://www.gilmorehealth.com/tetanus-vaccine-decreases-incidence-of-parkinsons-disease-and-slows-its-progression/ It is based on this paper: [u]
Tetanus vaccination
Very interesting article: [u]
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
[/u]
2024
https://www.gilmorehealth.com/tetanus-vaccine-decreases-incidence-of-parkinsons-disease-and-slows-its-progression/ It is based on this paper: [u]
Tetanus vaccination
Bolt_Upright
in
Cure Parkinson's
1 month ago
Infections like pneumonia and sinus. Lessons learned.
I’m saddened and sorry for all those who have been suffering from pneumonia and respiratory infections. Been posted of late. As a physician who knows better, I wish I’d followed my on advice to do ALL of the following 1. Test right away for COVID 2. Get a complete viral nasal swab to be tested
I’m saddened and sorry for all those who have been suffering from pneumonia and respiratory infections. Been posted of late. As a physician who knows better, I wish I’d followed my on advice to do ALL of the following 1. Test right away for COVID 2. Get a complete viral nasal swab to be tested
skipro
in
CLL Support
2 months ago
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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
8 months ago
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
8 months ago
Feel like giving up.
For unknown reasons other than we think Rituxumab is not working for you any more my medication was changed to Kevzera (Sarilulmab) in November. The work up checks were done and good to go apart from a Chest X Ray as I hadn't had one for a while. A shadow area was found on my lung with suspected
For unknown reasons other than we think Rituxumab is not working for you any more my medication was changed to Kevzera (Sarilulmab) in November. The work up checks were done and good to go apart from a Chest X Ray as I hadn't had one for a while. A shadow area was found on my lung with suspected
3LittleBirds2
in
NRAS
3 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
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
8 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
8 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
8 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
8 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
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
8 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
8 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
8 months ago
Bursitis of toes & Steroid Injection
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
sarahsch
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
Bursitis of the toes & Steroid Injection.
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
I've had pain from between the second & third toe since last May. It hurts to stand & walk especially barefoot or in shoes. I tend to wear trainers when I can as the base is soft & spongy. I had surgery Oct 22 for severe arthritis in the large toe & at first I feared it had spread. Two trips to GP (
sarahsch
in
LUPUS UK
3 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
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
8 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
8 months ago
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