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frustrated with restriction of naproxen
After an unsuccessful spinal fusion surgery in 2001(and 2 more since) I’ve been taking naproxen for about 15 years and get that together with a long list of other pain meds every 3 months,I’ve now been told I can only have 2 month supply of naproxen at a time which is messing up my repeat meds routine
After an unsuccessful spinal fusion surgery in 2001(and 2 more since) I’ve been taking naproxen for about 15 years and get that together with a long list of other pain meds every 3 months,I’ve now been told I can only have 2 month supply of naproxen at a time which is messing up my repeat meds routine
Paiger1
in
NRAS
1 year ago
Covid
Also know of 7 people who came away from a wedding with covid.
Also know of 7 people who came away from a wedding with covid.
Wantplaytennis
in
NRAS
1 year ago
Did Covid vaccination cause Fb/ME/CFS?
Hi everyone. Just wondering if there is anyone else out there who's Fb/ME/CFS started after their Covid vaccination!?
Hi everyone. Just wondering if there is anyone else out there who's Fb/ME/CFS started after their Covid vaccination!?
Bethenny
in
Fibromyalgia Action UK
1 year ago
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Cellulitis and ET
I’ve seen a nurse at my GP practice today (no doctors in!) I’ve got red swollen lower legs, that feel warm. She said it’s cellulitis and I’ve got antibiotics to take. Surprisingly she said she’d heard of ET, but just knew it was something to do with blood. Anyway apparently I’ve caught it early. She
I’ve seen a nurse at my GP practice today (no doctors in!) I’ve got red swollen lower legs, that feel warm. She said it’s cellulitis and I’ve got antibiotics to take. Surprisingly she said she’d heard of ET, but just knew it was something to do with blood. Anyway apparently I’ve caught it early. She
lizzziep
in
MPN Voice
1 year ago
Rage at GP
Sorry all I need to rant. Just back from GP appointment and I am outraged. Explained to him about my extreme levels of pain and his response was that people with "fibro" lead normal lives and that the diagnosis is given when the consultant doesn't know what's wrong with you!!! Said the pain clinic
Sorry all I need to rant. Just back from GP appointment and I am outraged. Explained to him about my extreme levels of pain and his response was that people with "fibro" lead normal lives and that the diagnosis is given when the consultant doesn't know what's wrong with you!!! Said the pain clinic
Macdoual
in
Fibromyalgia Action UK
10 months ago
New Hepatitis C page - British Liver Trust website
The
NEW
hepatitis C page is now live on the website. We're delighted to say that this came about with the involvement of one of our forum members, for which we're very grateful. Here's the link: https://britishlivertrust.org.uk/information-and-support/living-with-a-liver-condition/liver-conditions
The
NEW
hepatitis C page is now live on the website. We're delighted to say that this came about with the involvement of one of our forum members, for which we're very grateful. Here's the link: https://britishlivertrust.org.uk/information-and-support/living-with-a-liver-condition/liver-conditions
BritishLiverTrust1
Partner
in
British Liver Trust
1 year ago
Covid antivirals - why?
NHS have told me I have a condition that entitles me to antivirals for Covid. But haven't told me what is or which are the qualifying condition(s). GP doesn't know either. I think this is off! Makes me worry, and I'm not easily fazed. Is it an existing condition, if so which, or is it a new condition
NHS have told me I have a condition that entitles me to antivirals for Covid. But haven't told me what is or which are the qualifying condition(s). GP doesn't know either. I think this is off! Makes me worry, and I'm not easily fazed. Is it an existing condition, if so which, or is it a new condition
Coppernob
in
Aspergillosis and Rare Fungal Infection Support
1 year ago
Thoughts on L lysine
Hi everyone, I suffer from cold sores and I wanted to know if anybody take L lysine along with the valtrex or acyclovir ? I have been having one outbreak after another , just trying to get this to calm down. Any suggestions greatly appreciated. Thank you !
Hi everyone, I suffer from cold sores and I wanted to know if anybody take L lysine along with the valtrex or acyclovir ? I have been having one outbreak after another , just trying to get this to calm down. Any suggestions greatly appreciated. Thank you !
Jances13
in
LUPUS UK
10 months ago
covid
hi all. I have severe asthma. Which I have had for many years. I had covid in June last year. Followed by chest infection, then I was hospitalised with RSV. I spent all of Xmas in hospital after I also got flu a few weeks after that , I have never been right since I had covid. I went to the post
hi all. I have severe asthma. Which I have had for many years. I had covid in June last year. Followed by chest infection, then I was hospitalised with RSV. I spent all of Xmas in hospital after I also got flu a few weeks after that , I have never been right since I had covid. I went to the post
Denae011
in
Lung Conditions Community Forum
1 year ago
Dr appt updates
Saw my pulmonologist on Tues. “Why haven’t you been using your Cpap?” Me: “Sometimes I feel claustrophobic and it’s hard to breathe. I also have had shortness of breath since I had Covid last June after coming home from our trip.” This led her to have me do a 6 minute walking test - my oxygen didn’t
Saw my pulmonologist on Tues. “Why haven’t you been using your Cpap?” Me: “Sometimes I feel claustrophobic and it’s hard to breathe. I also have had shortness of breath since I had Covid last June after coming home from our trip.” This led her to have me do a 6 minute walking test - my oxygen didn’t
PWilli
in
My MSAA Community
1 year ago
Looking for a Surgeon with Specific Skills
This is a long shot. I’m an Aussie. I had HD brachytherapy for prostate cancer in 2010. In 2016, I was diagnosed with Carcinoma in Situ in the bladder. I’ve had multiple rounds of BCG, and I’m now heading towards a radical cystectomy. My urologist is nervous about the risk of damage to the rectum
This is a long shot. I’m an Aussie. I had HD brachytherapy for prostate cancer in 2010. In 2016, I was diagnosed with Carcinoma in Situ in the bladder. I’ve had multiple rounds of BCG, and I’m now heading towards a radical cystectomy. My urologist is nervous about the risk of damage to the rectum
Anthonyve
in
Advanced Prostate Cancer
10 months ago
Rash .
Hi I'm just looking for a bit of advice . I'm having a flare right now due to not being on my Biological drug since having an operation on my foot again . However this time seems longer and the flare is much more intense . Been up to see Rheumatology the Dr didn't know me didn't examine me even though
Hi I'm just looking for a bit of advice . I'm having a flare right now due to not being on my Biological drug since having an operation on my foot again . However this time seems longer and the flare is much more intense . Been up to see Rheumatology the Dr didn't know me didn't examine me even though
Weemillie
in
NRAS
1 year ago
Vaccination, Paxlovid decrease risk of long Covid, studies show
Vaccination, Paxlovid decrease risk of long Covid, studies show By Janelle Chavez, CNN Published 11:00 AM EDT, Thu March 23, 2023 https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html#:~:text
Vaccination, Paxlovid decrease risk of long Covid, studies show By Janelle Chavez, CNN Published 11:00 AM EDT, Thu March 23, 2023 https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html https://www.cnn.com/2023/03/23/health/long-covid-vaccination-paxlovid/index.html#:~:text
lankisterguy
Volunteer
in
CLL Support
1 year ago
fibro and covid
hi, I had Covid over Christmas 2021 (15 months ago) since then I constantly feel I’m in one long flare of relentless fatigue and pain whereas before I had times of feeling ‘better’. Anyone else noticed this since having covid? Thanks
hi, I had Covid over Christmas 2021 (15 months ago) since then I constantly feel I’m in one long flare of relentless fatigue and pain whereas before I had times of feeling ‘better’. Anyone else noticed this since having covid? Thanks
Belleross
in
Fibromyalgia Action UK
1 year ago
Hi, I'm new here. It all sucks a bit doesn't it!
In July 2020 I lost my Nan. She had a stroke and went to hospital, then a palliative nursing home. We couldn't go an visit because of stupid Covid. Only my Grandad could go, once a day, for an hour. She had 4 married sons, 4 grandchildren and 3 great grandchildren. She passed alone. Before that my Grandad
In July 2020 I lost my Nan. She had a stroke and went to hospital, then a palliative nursing home. We couldn't go an visit because of stupid Covid. Only my Grandad could go, once a day, for an hour. She had 4 married sons, 4 grandchildren and 3 great grandchildren. She passed alone. Before that my Grandad
Ronnietheblonde
in
Bereavement Care & Share
1 year ago
second vasectomy reversal- waiting results. Has anyone got a similar story?
My husband and I have been together 7 years. He had vasectomy from previous relationship, he is 11 years older than me and has a 13 y/o son. Fast forward us being together and me being only 26/27 he had a vasectomy reversal about 4 years after the vasectomy. It was successful and we have a beautiful
My husband and I have been together 7 years. He had vasectomy from previous relationship, he is 11 years older than me and has a 13 y/o son. Fast forward us being together and me being only 26/27 he had a vasectomy reversal about 4 years after the vasectomy. It was successful and we have a beautiful
Shaketheglitter
in
Fertility Network UK
10 months ago
long covid
My fibro had a flare that got a lot worse and stayed after I had covid in Dec 2021, and I now think this is a comorbidity esp as the symptoms overlap with fibro, but for me the severity and longevity has become so much worse since I had covid in a way my fibro never was before, the GP wanted to put everything
My fibro had a flare that got a lot worse and stayed after I had covid in Dec 2021, and I now think this is a comorbidity esp as the symptoms overlap with fibro, but for me the severity and longevity has become so much worse since I had covid in a way my fibro never was before, the GP wanted to put everything
DavidCB
in
Fibromyalgia Action UK
1 year ago
Not sure what to expect?
Hi all I’ve managed to get an appointment with the Rheumy nurse today f2f. I started on Sulfasalazine just over 2 years ago, I was slow to improve and had steroid injections to help along the way. I changed trusts after one year due to lack of appointments and just general mayhem prompted by my GP.
Hi all I’ve managed to get an appointment with the Rheumy nurse today f2f. I started on Sulfasalazine just over 2 years ago, I was slow to improve and had steroid injections to help along the way. I changed trusts after one year due to lack of appointments and just general mayhem prompted by my GP.
Akaka
in
NRAS
1 year ago
Persistent cough
Hi All, I don't know of anyone can assist me in this complex enquiry, I will give it a try and keep it brief. I have CLL and am seeing my Haematologist on Monday, regarding persistent cough, night and day sweats, and a viral infection I have had on and off for 6 months. I have had a Chest X Ray and
Hi All, I don't know of anyone can assist me in this complex enquiry, I will give it a try and keep it brief. I have CLL and am seeing my Haematologist on Monday, regarding persistent cough, night and day sweats, and a viral infection I have had on and off for 6 months. I have had a Chest X Ray and
Vindicatrix
in
Lung Conditions Community Forum
11 months ago
"A revolution in cancer treatment?"
I don't see a specific reference to prostate cancer in this article in today's NYTimes. But it's about multiple cancers, and the idea, spoken of here before, is that patients with cancers formerly called terminal are living longer and longer as multiple drug treatments may come close to turning these
I don't see a specific reference to prostate cancer in this article in today's NYTimes. But it's about multiple cancers, and the idea, spoken of here before, is that patients with cancers formerly called terminal are living longer and longer as multiple drug treatments may come close to turning these
billfenley2
in
Advanced Prostate Cancer
10 months ago
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