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⭐️⭐️my COVID journey ⭐️⭐️
⭐️covid survivors let’s keep on fighting, let’s help each other & spread awareness of the real impact & life changing difficulties we face❤️❤️ Ladysurvivor1 profile image Ladysurvivor1 2 days ago•0 Replies 🧏🏽♀️My COVID Journey: A Tale of Resilience and Hope (Part 1) In the depths of January
⭐️covid survivors let’s keep on fighting, let’s help each other & spread awareness of the real impact & life changing difficulties we face❤️❤️ Ladysurvivor1 profile image Ladysurvivor1 2 days ago•0 Replies 🧏🏽♀️My COVID Journey: A Tale of Resilience and Hope (Part 1) In the depths of January
Ladysurvivor1
in
ICUsteps
6 months ago
Finally failed at side-stepping the “rona”
Well I guess sooner or later it had to happen. Four years of avoiding covid and now I caught it whilst traveling for work in the Far East. Started with a cold and a general malaise, then a few days later, last night, I had a slight temperature so I thought I’d check (had packed some tests just in
Well I guess sooner or later it had to happen. Four years of avoiding covid and now I caught it whilst traveling for work in the Far East. Started with a cold and a general malaise, then a few days later, last night, I had a slight temperature so I thought I’d check (had packed some tests just in
Aldebaran25
in
MPN Voice
6 months ago
Stomach pain common with IBS?
Is stomach pain common with IBS?If so, where do you feel the pain? I feel pain right in the center pit of my stomach... sometimes gnawing sensation, sometimes a cramping sensation Do you feel it there in the center pit of your stomach too?
Is stomach pain common with IBS?If so, where do you feel the pain? I feel pain right in the center pit of my stomach... sometimes gnawing sensation, sometimes a cramping sensation Do you feel it there in the center pit of your stomach too?
Catsandsunsets
in
IBS Network
3 months ago
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Famotidine
I have been on 20mg of Famotidine for about a year, over the past 6 months while taking Famotidine I seem to have developed heartburn has any one else suffered with heartburn while on Famotidine? I was on Omeprazole previously for nearly 3 years without any problems but a blood test revealed low sodium
I have been on 20mg of Famotidine for about a year, over the past 6 months while taking Famotidine I seem to have developed heartburn has any one else suffered with heartburn while on Famotidine? I was on Omeprazole previously for nearly 3 years without any problems but a blood test revealed low sodium
Phed
in
PMRGCAuk
3 months ago
Shingles vaccine and atrial fibrillation
Hi, My GP is recommending shingles vaccine. I am just concerned if it will cause atrial fibrillation. Any one had shingles vaccines with no adverse effects like atrial fibrillationThanks Padma
Hi, My GP is recommending shingles vaccine. I am just concerned if it will cause atrial fibrillation. Any one had shingles vaccines with no adverse effects like atrial fibrillationThanks Padma
Poluneeru
in
Atrial Fibrillation Support
3 months ago
Worried About (Possible) Recent Diagnosis of PMR.
Around 3 months ago I became aware of increasing aches and pains in my arms and legs and an overwhelming exhaustion. I’m normally a fit and active 73 year old. My neck felt stiff but I put that down to wear and tear as I also have worn discs in my lower spine which I manage with Pilates. GP sent me
Around 3 months ago I became aware of increasing aches and pains in my arms and legs and an overwhelming exhaustion. I’m normally a fit and active 73 year old. My neck felt stiff but I put that down to wear and tear as I also have worn discs in my lower spine which I manage with Pilates. GP sent me
GlesgaGal
in
PMRGCAuk
6 months ago
Shingles
I posted over 9 weeks ago about my shingles outbreak. I still have horrible pain and can't stand clothing even to touch me. I have had 2 epidurals for the pain and they didn't even help at all. Someone wrote back and said that they had shingles since last December and I couldn't find the post. If you
I posted over 9 weeks ago about my shingles outbreak. I still have horrible pain and can't stand clothing even to touch me. I have had 2 epidurals for the pain and they didn't even help at all. Someone wrote back and said that they had shingles since last December and I couldn't find the post. If you
mlp3434
in
Atrial Fibrillation Support
3 months ago
Interesting article about the effects of Covid19 on your blood
Having caught Covid19 a short time after my allo SCT and with my anaemia ongoing, I was interested to see this article. This is not CLL specific but worth a read. "[i]Several studies have reported, in COVID-19 patients, hematological abnormalities. Most of these alterations are associated with a higher
Having caught Covid19 a short time after my allo SCT and with my anaemia ongoing, I was interested to see this article. This is not CLL specific but worth a read. "[i]Several studies have reported, in COVID-19 patients, hematological abnormalities. Most of these alterations are associated with a higher
Jm954
Administrator
in
CLL Support
6 months ago
covid vaccine and prostate cancer
I was surprised that the post about the covid vaccine was abruptly terminated as if the subject was closed and the answer is settled. That is not true in my opinion. This is a brand new technology that was only tested for about a year. No definitive study has been done about the long term impact (if
I was surprised that the post about the covid vaccine was abruptly terminated as if the subject was closed and the answer is settled. That is not true in my opinion. This is a brand new technology that was only tested for about a year. No definitive study has been done about the long term impact (if
Schwah
in
Advanced Prostate Cancer
6 months ago
covid vaccine & prostate cancer
Any concerns/studies re covid vaccines bringing prostate cancer back? No politics just want to know if there are any reasons to be concerned.
Any concerns/studies re covid vaccines bringing prostate cancer back? No politics just want to know if there are any reasons to be concerned.
BL2023
in
Advanced Prostate Cancer
6 months ago
Next instalment. I thought I`d better do this now before I start working.
In fact, I don't remember ever seeing my dad drunk, except for one occasion when he had had, perhaps, an excess of drink. We were on a family holiday in Ireland, in a horse drawn caravan, which in itself was an experience, especially for the horse as we had no prior experience whatsoever of the care
In fact, I don't remember ever seeing my dad drunk, except for one occasion when he had had, perhaps, an excess of drink. We were on a family holiday in Ireland, in a horse drawn caravan, which in itself was an experience, especially for the horse as we had no prior experience whatsoever of the care
LissacFrance
in
Lung Conditions Community Forum
4 months ago
Travelling with interferon/pegasys
Hi , I have just recently started on the pegasys weekly injections . I am travelling to Greece and wonder if anyone can recomend the best way to keep the medication at the correct temperature whilst flying and travelling. Is there a chargeable medication box which I could charge using a battery pack
Hi , I have just recently started on the pegasys weekly injections . I am travelling to Greece and wonder if anyone can recomend the best way to keep the medication at the correct temperature whilst flying and travelling. Is there a chargeable medication box which I could charge using a battery pack
Sunnyhunny
in
MPN Voice
4 months ago
Over heating
I have been suffering from overheating since I had covid in 2022, thought it was my HRT tablets but wasn't (doctor has since taken me off them, another story) and has gotten worse over the period from then until now. I start sweating no matter what the weather or temperature is day and night, I can
I have been suffering from overheating since I had covid in 2022, thought it was my HRT tablets but wasn't (doctor has since taken me off them, another story) and has gotten worse over the period from then until now. I start sweating no matter what the weather or temperature is day and night, I can
pramela
in
Pernicious Anaemia Society
6 months ago
common cold lingers
back in April 2020 i had covid the first time (that was early before we knew anything) since then when i get a cold (head cold, sinus infection, common cold) i notice that i feel bad for like 3-5 days but i will have a lingering cough for like a 5-10 days afterwards. i was blaming it on covid and the
back in April 2020 i had covid the first time (that was early before we knew anything) since then when i get a cold (head cold, sinus infection, common cold) i notice that i feel bad for like 3-5 days but i will have a lingering cough for like a 5-10 days afterwards. i was blaming it on covid and the
pete-paz
in
CLL Support
23 days ago
Streptococcal Bacterial Meningitis
Hi, everyone! I was admitted to the hospital on March 11 and diagnosed with Streptococcal Bacterial Meningitis and hospitalized for 17 days. Just released last Thursday. This was all brought on by an ear infection that I guess turned into meningitis. I had all the tests and scans and was told I was lucky
Hi, everyone! I was admitted to the hospital on March 11 and diagnosed with Streptococcal Bacterial Meningitis and hospitalized for 17 days. Just released last Thursday. This was all brought on by an ear infection that I guess turned into meningitis. I had all the tests and scans and was told I was lucky
Fjreed23
in
Meningitis Now
4 months ago
Interferon and the liver
question to all my MPN people on here who are taking pegasys or besremi, how do you manage elevated liver enzymes? Do they cycle up and down? Is there anything we can do to bring them down? What is acceptable to y’all? My hematologist says not to worry until they hit 2-300.. My blood numbers actually
question to all my MPN people on here who are taking pegasys or besremi, how do you manage elevated liver enzymes? Do they cycle up and down? Is there anything we can do to bring them down? What is acceptable to y’all? My hematologist says not to worry until they hit 2-300.. My blood numbers actually
dbus1417
in
MPN Voice
4 months ago
⭐️covid survivors let’s keep on fighting, let’s help each other & spread awareness of the real impact & life changing difficulties we face
🧏🏽♀️My COVID Journey: A Tale of Resilience and Hope (Part 1) In the depths of January 2021, my life took an unexpected turn when I found myself in the clutches of COVID-19. At first, I mistook the weakening of my body for a mere exacerbation of my asthma. Little did I know that this was just the
🧏🏽♀️My COVID Journey: A Tale of Resilience and Hope (Part 1) In the depths of January 2021, my life took an unexpected turn when I found myself in the clutches of COVID-19. At first, I mistook the weakening of my body for a mere exacerbation of my asthma. Little did I know that this was just the
Ladysurvivor1
in
ICUsteps
6 months ago
Finger nails and raynauds
Hi ..I have raynauds and limited schleroderma and was wondering if anyone has the problem of there finger nails being discoloured and lifting off the nail bed ..I have tried lots of treatments but nothing seems to work and am now worried that I may lose some nails altogether!
Hi ..I have raynauds and limited schleroderma and was wondering if anyone has the problem of there finger nails being discoloured and lifting off the nail bed ..I have tried lots of treatments but nothing seems to work and am now worried that I may lose some nails altogether!
Tmontana
in
Scleroderma & Raynaud's UK (SRUK)
4 months ago
clavicle/collar bone swelling - YouTube Vid
hi there, A few of us have been talking about swelling in the pits of the collar bone. Instagram must’ve been listening 👂🏼 as this expert popped up in my feed. apparently this area is called the terminus, left and right so different jobs. I’ve watched this YouTube and immediately had gunk running
hi there, A few of us have been talking about swelling in the pits of the collar bone. Instagram must’ve been listening 👂🏼 as this expert popped up in my feed. apparently this area is called the terminus, left and right so different jobs. I’ve watched this YouTube and immediately had gunk running
Regenallotment
in
Thyroid UK
4 months ago
Winter or Spring Covid Booster Vaccinations?
Winter or Spring Covid Booster Vaccinations? Good evening everyone, has anyone heard anything about "Covid Boosters Vaccinations" being available for Winter or Spring? The last Booster I received was early October 2023 as I have a weakened immune system. I have not seen much coverage on this by the
Winter or Spring Covid Booster Vaccinations? Good evening everyone, has anyone heard anything about "Covid Boosters Vaccinations" being available for Winter or Spring? The last Booster I received was early October 2023 as I have a weakened immune system. I have not seen much coverage on this by the
Joseph260268
in
Lung Conditions Community Forum
6 months ago
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