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cellulitis
Hello, Has anyone had cellulitis? I have had it for just over a week. I have just completed a 2 day course of Ciprobay 500 and it didn’t work then I had a 2 day of Meronam 1gm tds by injection and I can tell it works good. Now, I need your advice if I can travel for a week with my oral antibiotic Augmentin
Hello, Has anyone had cellulitis? I have had it for just over a week. I have just completed a 2 day course of Ciprobay 500 and it didn’t work then I had a 2 day of Meronam 1gm tds by injection and I can tell it works good. Now, I need your advice if I can travel for a week with my oral antibiotic Augmentin
ANA4
in
CLL Support
5 months ago
Covid booster and steroids
I have been offered my Covid booster for next Monday but I had a steroid injection on March 25th. Does anyone know if I need to leave longer between the two jabs??
I have been offered my Covid booster for next Monday but I had a steroid injection on March 25th. Does anyone know if I need to leave longer between the two jabs??
Spin1959
in
NRAS
29 days 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
1 month ago
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Covid!!!!
Hubby and I were both enjoying a long overdue week in the sunshine - 4 days into the holiday hubby developed a sore throat and a cough, and a few shivers. Temperature ok… Roll forward 2 days and my AF was kicking off in spite of medication. Home today and both of us tested positive for Covid. Fortunately
Hubby and I were both enjoying a long overdue week in the sunshine - 4 days into the holiday hubby developed a sore throat and a cough, and a few shivers. Temperature ok… Roll forward 2 days and my AF was kicking off in spite of medication. Home today and both of us tested positive for Covid. Fortunately
Fight-the-good-fight
in
Atrial Fibrillation Support
18 hours ago
COVID vaccination
I think all of these horrible symptoms we have are the results of COVID-19 vaccination. I’m so angry 😡
I think all of these horrible symptoms we have are the results of COVID-19 vaccination. I’m so angry 😡
Sissiotto
in
Pernicious Anaemia Society
2 days ago
Covid Vaccine help and advice please 😊
I have had a week of ill health (hellish) following every vaccine but my body seems to accept the Pfizer !! so this time round was hopeful. However there is none to be had . I have been offered the Moderna , has anyone else who has systemic lupus had this one ? And can you tell me how you were ? I just
I have had a week of ill health (hellish) following every vaccine but my body seems to accept the Pfizer !! so this time round was hopeful. However there is none to be had . I have been offered the Moderna , has anyone else who has systemic lupus had this one ? And can you tell me how you were ? I just
Maddymay65
in
LUPUS UK
2 days ago
Neuropathy worse after covid jab, anyone?
After my recent ninth Covid jab (second time with Moderna), I found I had reactions (have always had none before, lucky me). First I developed the grandly named"Covid arm" which was nothing much, just a faint, occasional itch around the jab area which disappeared after a week. Then, for about a week
After my recent ninth Covid jab (second time with Moderna), I found I had reactions (have always had none before, lucky me). First I developed the grandly named"Covid arm" which was nothing much, just a faint, occasional itch around the jab area which disappeared after a week. Then, for about a week
Trickysite
in
My Ovacome
4 days ago
Covid Vax and age
I’m in the US and have lupus and many other disqualifying illnesses 😊. I just read a thread in which folks thought their PMR began with Covid jabs. After 3 Moderna, and 3 bouts of Covid I don’t think I want to get vaccinated again. But then there’s flirt. I have 2 grandchildren ages 5 and 4 with long
I’m in the US and have lupus and many other disqualifying illnesses 😊. I just read a thread in which folks thought their PMR began with Covid jabs. After 3 Moderna, and 3 bouts of Covid I don’t think I want to get vaccinated again. But then there’s flirt. I have 2 grandchildren ages 5 and 4 with long
MrsMarigold
in
PMRGCAuk
5 days ago
Protection from Coronaviruses That Haven’t Yet Emerged
To paraphrase Ozzy Osbourne, pandemics can spring up without warning. Although 101 years separated the most recent, truly global pandemics - the H1N1 virus killing tens of millions of people from 1918 to 1920 and SARS-COV2 killing an estimated 14.8 million people in 2020-21 alone https://www.ncbi.nlm.nih.gov
To paraphrase Ozzy Osbourne, pandemics can spring up without warning. Although 101 years separated the most recent, truly global pandemics - the H1N1 virus killing tens of millions of people from 1918 to 1920 and SARS-COV2 killing an estimated 14.8 million people in 2020-21 alone https://www.ncbi.nlm.nih.gov
bennevisplace
in
CLL Support
5 days 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)
2 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
2 months ago
Update- Moderna Spikevax
Just to update. Received blood result and all within rang with the exception of Lymphocyte count which 3.1 only slightly over range. CPR 4 g/L, ESR 2. Which rules out PMR flare. So onwards and upwards, definitely downwards with Pred.-so pleased. I am now wondering whether the muscle paralysis I had
Just to update. Received blood result and all within rang with the exception of Lymphocyte count which 3.1 only slightly over range. CPR 4 g/L, ESR 2. Which rules out PMR flare. So onwards and upwards, definitely downwards with Pred.-so pleased. I am now wondering whether the muscle paralysis I had
Pebblegod
in
PMRGCAuk
6 days ago
COVID diagnosis
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Just been on a 300 mile bike ride and returned with COVID. Don't feel too bad but should I contact consultant. I have had a vaccination about 3 weeks ago.
Guinness4822
in
CLL Support
6 days ago
COVID, FND, and Cymbalta Ruined My Life
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
This is a long story, and I apologize in advance for any, bitter angry undertones. I'll skip all of the grief I've had in life and the hard times that I've experienced. I'll try to keep it to the medical issues. It will feel good to tell a part of my story, arguably the hardest I've been through.***Trigger
LoverOfAllThings
in
Functional Neurological Disorder - FND Hope
6 days ago
Increase in Synthroid Dose Worse Before Feeling Better?
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Hello, I'm a long time hypothyroid patient but the last few years after covid have been a wild ride finding the right dose again. I'm curious if anyone can offer insight as to why the first one to two weeks of a medication dose increase I feel amazing and then I tank horribly after. All the hypo symptoms
Clarabethk
in
Thyroid UK
7 days ago
Hello
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse
Hello again Hi. Ive had to shut down and rejoin the group. HU was playing up. Here is my original post. Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are so varied. Mine are mild but have been getting progressively worse
Trish_PBG
in
FND Action
7 days ago
Hello again
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Hi. Ive had to shut down and rejoin the group. HU was,playing up. I have such great comments and ideas,already from Lady4 and others, so thank you. Below was, my original post Hello Everyone,I have just joined this group and look forward to reading your journey's with coping with FND. The symptoms are
Trish_PBG
in
Functional Neurological Disorder - FND Hope
7 days ago
covid booster (Maderna)
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
morning all!! I have RA and I’m booked in for my annual covid booster!my concern is that from day one I’ve always had Pfizer vaccine but apparently there not using it this time around and it’s been replaced with Maderna it just makes me feel uneasy as I never had any problems with Pfizer!!have any you
Mybirthday1975
in
NRAS
7 days ago
Omicron variant
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
Hi all I have bronchiectasis (since 2012) and have been super careful during the pandemic. However, I missed my last vaccine (having had 4 over the years as well as both flu and shingles jabs) as the nearest place the NHS website could offer me for the 5th Covid jab was 22 miles away! With no public
swimmer
in
Lung Conditions Community Forum
8 days ago
Scared and lost
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Hello, I am not too sure where to start, so much has happened. I am a 50 year-old female. A couple of years ago, I had a pain in my abdomen on the right side and my stools became orange. The GP sent me for an ultrasound where they saw I had polyps on my gallbladder. The GP phoned me on the 31st Dec to
Foi24
in
British Liver Trust
9 days ago
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