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angular cheilitis
I’ve suffer a lot from this I get it around 3/4 times a year but usually lasts about a week. I’m on my third week struggling with this and can’t find a lip balm or treatment. I heard Daktarin oral gel but it’s sold out everywhere and the pharmacy said they even finding it hard to get it in for people
I’ve suffer a lot from this I get it around 3/4 times a year but usually lasts about a week. I’m on my third week struggling with this and can’t find a lip balm or treatment. I heard Daktarin oral gel but it’s sold out everywhere and the pharmacy said they even finding it hard to get it in for people
Ladybitsandbobs
in
NRAS
6 months ago
Health Anxiety or MS
Hi All, Since 2013... my life has been somewhat a constant fear of one disease or the other. Thank to Doc google. I havent had a night in peace for the last atleast 10 years. It started in 2013 with lightheadedness which made me go to an ent. He said symptoms are of bppv and prescribed some medicines
Hi All, Since 2013... my life has been somewhat a constant fear of one disease or the other. Thank to Doc google. I havent had a night in peace for the last atleast 10 years. It started in 2013 with lightheadedness which made me go to an ent. He said symptoms are of bppv and prescribed some medicines
Muef
in
Anxiety and Depression Support
3 months ago
Covid and Thyroid
I don’t have research but a personal story. My daughter who is 23 contracted Covid last summer and I noticed she was really having a tough time. Went to the doctor was on the way to recovery and then rebounded I noticed she lost close to 30 pounds in three weeks. She started feeling better again but
I don’t have research but a personal story. My daughter who is 23 contracted Covid last summer and I noticed she was really having a tough time. Went to the doctor was on the way to recovery and then rebounded I noticed she lost close to 30 pounds in three weeks. She started feeling better again but
hokulani0710
in
Thyroid UK
3 months ago
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Pegasys for MF transitioning from hydroxycarbamide
My darling wife, had her appointment today, and her blood is well below par her Hgb is 82 hematocrit 0.27, platelets 213 which is good, white cells 45. The hematologist was talking about introducing pegasys interferon injections, after her 3 bags of red cells and a ferinject. She is worried about losing
My darling wife, had her appointment today, and her blood is well below par her Hgb is 82 hematocrit 0.27, platelets 213 which is good, white cells 45. The hematologist was talking about introducing pegasys interferon injections, after her 3 bags of red cells and a ferinject. She is worried about losing
jointpain
in
MPN Voice
6 months ago
My first COVID positive test ever came up twice positive
I thought I had a cold coming Wednesday night while at work at the local hospital, then yesterday had my rutuximab at the local chemo unit told them about my cold, they were happy to carry on , I did test on Wednesday evening at work negative Tested today twice both positive Been aching a lot especially
I thought I had a cold coming Wednesday night while at work at the local hospital, then yesterday had my rutuximab at the local chemo unit told them about my cold, they were happy to carry on , I did test on Wednesday evening at work negative Tested today twice both positive Been aching a lot especially
Stewie_1968
in
CLL Support
3 months ago
Shingles Vaccination UK
Hi I am glad to report that I needed no hospital admissions in 2023 (having had 4 in 2022) Decided after open ended discussion with my GP not to take Covid or Flu vaccinations as each one had in the past laid me up with fever etc for a week to ten days and feeling dreadful. Next up is an offer of
Hi I am glad to report that I needed no hospital admissions in 2023 (having had 4 in 2022) Decided after open ended discussion with my GP not to take Covid or Flu vaccinations as each one had in the past laid me up with fever etc for a week to ten days and feeling dreadful. Next up is an offer of
Hihohiho
in
CLL Support
6 months ago
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
6 months ago
TINGLY FEET
Has anyone on here experienced tingly feet during the night after having steroid injections in the knees. I had the injections in both of my knees for arthritis only four days ago. The tingly feeling seems just like having a flare when I need to increase my steroids. It goes as soon as I get up in the
Has anyone on here experienced tingly feet during the night after having steroid injections in the knees. I had the injections in both of my knees for arthritis only four days ago. The tingly feeling seems just like having a flare when I need to increase my steroids. It goes as soon as I get up in the
Wallydb
in
PMRGCAuk
3 months ago
Covid vaccine
Hi haven’t been on for a while -all the Healthunlocked notifications going into junk - so not been prompted! Does anyone know when we can get next Covid booster -my lady was 6 months ago. I seem to recall something about a spring booster ? Thank you ! Happy Easter—have a lovely April x
Hi haven’t been on for a while -all the Healthunlocked notifications going into junk - so not been prompted! Does anyone know when we can get next Covid booster -my lady was 6 months ago. I seem to recall something about a spring booster ? Thank you ! Happy Easter—have a lovely April x
Mozart150
in
NRAS
3 months ago
Is this gastritis???
Hello, I'm new to this group. I caught (1st time) covid 19 this past Christmas 2023. It took me 3 weeks to recover. On the tail end I notice I pretty much lost my appetite then my symptoms upper middle abdomen area (diaphragm) daily bloating, fullness, dull pain, nausea, no appetite, shortness of breath
Hello, I'm new to this group. I caught (1st time) covid 19 this past Christmas 2023. It took me 3 weeks to recover. On the tail end I notice I pretty much lost my appetite then my symptoms upper middle abdomen area (diaphragm) daily bloating, fullness, dull pain, nausea, no appetite, shortness of breath
Marc787
in
IBS Network
3 months ago
Hyberbaric Oxygen Therapy
I have a friend who contracted Lyme disease and recently underwent a series of hyperbaric oxygen therapy sessions. The treatment has completely transformed him and he is now his old self. I have read that this therapy helps Fibromyalgia and other autoimmune diseases and was wondering if anyone knew
I have a friend who contracted Lyme disease and recently underwent a series of hyperbaric oxygen therapy sessions. The treatment has completely transformed him and he is now his old self. I have read that this therapy helps Fibromyalgia and other autoimmune diseases and was wondering if anyone knew
Lassie2
in
PMRGCAuk
2 days ago
Voice volume issues post ICU
Hello! I was in ICU in February. I thought I just had a bad cough… I’d lost my voice and thrown up and felt shocking and my GP told me it was viral and to take aspirin. Two days later, I was blue-lighted to hospital with Flu, severe pneumonia, strep A and sepsis. I went into septic shock and was put
Hello! I was in ICU in February. I thought I just had a bad cough… I’d lost my voice and thrown up and felt shocking and my GP told me it was viral and to take aspirin. Two days later, I was blue-lighted to hospital with Flu, severe pneumonia, strep A and sepsis. I went into septic shock and was put
Lucindar
in
ICUsteps
4 days ago
does a dreadful cold affect GCA
I have
dreadful
cold ,sore throat congestion in my nose fatigue.i am going for bloods on Monday perhaps wait till I feel stronger.
I have
dreadful
cold ,sore throat congestion in my nose fatigue.i am going for bloods on Monday perhaps wait till I feel stronger.
Bluemoon2023
in
PMRGCAuk
5 days ago
shingles jab anyone?
I had a very bad bout of shingles three years ago. Yesterday my doctors surgery rang to say I qualified for a jab! I tried to ask if it was worthwhile for someone who had already had shingles and was told she was the receptionist! Fair enough but then you can’t speak to a medic anymore Any thoughts
I had a very bad bout of shingles three years ago. Yesterday my doctors surgery rang to say I qualified for a jab! I tried to ask if it was worthwhile for someone who had already had shingles and was told she was the receptionist! Fair enough but then you can’t speak to a medic anymore Any thoughts
Green230461
in
NRAS
12 days ago
Chondocalcitis incurable?
At least that's how I think it's spelt. It's a specialised form of RA and I have it in my left knee (along with normal RA in shoulders, elbows, wrists and fingers.It's also called Pseudogout but as the crystals in Chondocalcitis are calcium they can't be dispersed as the uric acid crystals in ordinary
At least that's how I think it's spelt. It's a specialised form of RA and I have it in my left knee (along with normal RA in shoulders, elbows, wrists and fingers.It's also called Pseudogout but as the crystals in Chondocalcitis are calcium they can't be dispersed as the uric acid crystals in ordinary
Jeff1943
in
NRAS
3 months ago
Emergency use authorization of a new pre-exposure prophylaxis (PrEP) for COVID-19, PEMGARDA™ (VYD222)
Hi, Great news for the immunocompromised community including us. Invivyd announced late last week the emergency use authorization of their new pre-exposure prophylaxis (PrEP) for COVID-19, PEMGARDA™ (VYD222). It’s a one-hour infusion and lasts 3 months and based on titers should be effective against
Hi, Great news for the immunocompromised community including us. Invivyd announced late last week the emergency use authorization of their new pre-exposure prophylaxis (PrEP) for COVID-19, PEMGARDA™ (VYD222). It’s a one-hour infusion and lasts 3 months and based on titers should be effective against
bkoffman
CLL CURE Hero
in
CLL Support
3 months ago
Getting Off of Painkillers
I started seeing a pain management doctor about 4 years ago for severe lower back pain. One of the first things she did was put me on 5 mg Hydrocodone four times a day and gave me a steroid injection. Over the years, I have had several radio frequency ablations and a handful of steroid injections. The
I started seeing a pain management doctor about 4 years ago for severe lower back pain. One of the first things she did was put me on 5 mg Hydrocodone four times a day and gave me a steroid injection. Over the years, I have had several radio frequency ablations and a handful of steroid injections. The
Hidden
in
Pain Concern
3 months ago
Flu and Pneumonia vaccinations
I was wondering if having the Flu shot or Pneumonia shot causes AFib episodes like COVID did.
I was wondering if having the Flu shot or Pneumonia shot causes AFib episodes like COVID did.
Shayshell
in
Atrial Fibrillation Support
17 days ago
Covid and injections
I suffered from Covid over Christmas from the 16th to the 30th December. Up 'til now I have had all the injections on offer. I read Dorset Lady's post that we are going to be offered another injection in the spring. It has left me wondering whether I will need this or not in the circumstances. I
I suffered from Covid over Christmas from the 16th to the 30th December. Up 'til now I have had all the injections on offer. I read Dorset Lady's post that we are going to be offered another injection in the spring. It has left me wondering whether I will need this or not in the circumstances. I
prunus
in
PMRGCAuk
3 months ago
Tetanus
Not too far back there was a discussion about having a Tetanus shot, might help PD. I tried a search and came up with only one 2 year old post. No very Techy. Can someone help me find the link to that discussion? Thank you
Not too far back there was a discussion about having a Tetanus shot, might help PD. I tried a search and came up with only one 2 year old post. No very Techy. Can someone help me find the link to that discussion? Thank you
Ghmac
in
Cure Parkinson's
19 days ago
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