Search
Search
About
Log in
Join
Experiences with
Pneumococcal infections
Posts
Communities
28,887 public posts
Filter results
Pneumococcal vaccine
Hi everyone , can anyone tell me if the pneumococcal vaccine is safe ? I have uctd and triple positive APS thanks Elfie
Hi everyone , can anyone tell me if the pneumococcal vaccine is safe ? I have uctd and triple positive APS thanks Elfie
Elfie1
in
Hughes Syndrome APS Forum
3 months ago
High-Dose Vitamin D Linked to Lower Disease Activity in CIS
High-dose oral cholecalciferol (vitamin D3) supplementation significantly reduces evidence of disease activity in patients with clinically isolated syndrome (CIS), results of a randomized, controlled trial suggest. In addition, cholecalciferol had a favorable safety profile and was well tolerated.
High-dose oral cholecalciferol (vitamin D3) supplementation significantly reduces evidence of disease activity in patients with clinically isolated syndrome (CIS), results of a randomized, controlled trial suggest. In addition, cholecalciferol had a favorable safety profile and was well tolerated.
BettysMom
in
My MSAA Community
2 days ago
Off label uses for Inbrija?
I've just started experimenting with Inbrijia. So far, so good for a rescue med. I seem to be back on in 10-15 mins with one toke. Has any one experimented with Inbrija for other uses? For example, I think it would work great for those times when I eat a meal with protein and then realize it's time
I've just started experimenting with Inbrijia. So far, so good for a rescue med. I seem to be back on in 10-15 mins with one toke. Has any one experimented with Inbrija for other uses? For example, I think it would work great for those times when I eat a meal with protein and then realize it's time
ktbooks77
in
Cure Parkinson's
2 days ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Post viral fatigue
I'm a Newby to the group,my story goes.For years I get a mild infection just like a cold coming on which then passes after a few days but I'm left with this terrible fatigue, I can't evan have a conversation with my husband without getting exhausted, this year it lasted 4 months,the first 2 months I
I'm a Newby to the group,my story goes.For years I get a mild infection just like a cold coming on which then passes after a few days but I'm left with this terrible fatigue, I can't evan have a conversation with my husband without getting exhausted, this year it lasted 4 months,the first 2 months I
Toastwithbutter
in
Women's Health
3 days ago
Purpura or Shingles?
I have had purpura rashes before but this one is bigger. It’s on my arm better elbow & wrist.A friend said could it be shingles. That hadn’t occurred to me, anyone got any thoughts. It was a bit itchy when it first appeared yesterday but ok now.. Thanks
I have had purpura rashes before but this one is bigger. It’s on my arm better elbow & wrist.A friend said could it be shingles. That hadn’t occurred to me, anyone got any thoughts. It was a bit itchy when it first appeared yesterday but ok now.. Thanks
Baner
in
PMRGCAuk
4 days ago
Follow up on the IFN types, Options
I noted in that post a thought of using a non pegylated IFN as a temporary measure as Pegasys becomes unavailable. It may not be so out-of-the-box thinking. This reference shows its use, and provides a dose schedule and relative dosing vs PEG. If you are out of viable options, (cannot access Bes or
I noted in that post a thought of using a non pegylated IFN as a temporary measure as Pegasys becomes unavailable. It may not be so out-of-the-box thinking. This reference shows its use, and provides a dose schedule and relative dosing vs PEG. If you are out of viable options, (cannot access Bes or
EPguy
in
MPN Voice
6 days ago
Interferon types, Old and New, what are the options?
In some recent threads this has come up in context of the PEG shortage and there is some confusion. For those interested here are some thoughts on MPN interferon versions. -- There are a many different types of IFNs, with various Greek letters and type classes. For MPNs only two among these many
In some recent threads this has come up in context of the PEG shortage and there is some confusion. For those interested here are some thoughts on MPN interferon versions. -- There are a many different types of IFNs, with various Greek letters and type classes. For MPNs only two among these many
EPguy
in
MPN Voice
7 days ago
Exhausted 6 wk flare up post Gastroenteritis
I'm utterly physically and mentally exhausted. Had lifelong IBS and had flare ups in the past but nothing like this! Got viral gastroenteritis on holiday 6 wks ago. Since then have spent 3wks in hospital with D&V trying to get on top of it, the pain and hydration. I've lost a stone and half. I'm being
I'm utterly physically and mentally exhausted. Had lifelong IBS and had flare ups in the past but nothing like this! Got viral gastroenteritis on holiday 6 wks ago. Since then have spent 3wks in hospital with D&V trying to get on top of it, the pain and hydration. I've lost a stone and half. I'm being
Happystart
in
IBS Network
9 days ago
IPF Blood Tests
recently had an extensive blood test, in preparation for starting medicine that is supposed to delay the IPF. About 4 items were slightly outside the range. Not unusual. A few days later another item was added. Aspergillosis igG, a reading of 82, the max limit is 40. I have been told i don’t need any
recently had an extensive blood test, in preparation for starting medicine that is supposed to delay the IPF. About 4 items were slightly outside the range. Not unusual. A few days later another item was added. Aspergillosis igG, a reading of 82, the max limit is 40. I have been told i don’t need any
Goto4
in
Lung Conditions Community Forum
10 days ago
Persistent trace/low level protein in urine
Hi all I've had persistent trace or low level amounts of protein in urine tests since April -checked on 5 occasions at hospital. Sometimes there is also trace amounts of blood or white cells too. Is this something to worry about or just part of the disease? I get cystitis a lot, but doesn't necessarily
Hi all I've had persistent trace or low level amounts of protein in urine tests since April -checked on 5 occasions at hospital. Sometimes there is also trace amounts of blood or white cells too. Is this something to worry about or just part of the disease? I get cystitis a lot, but doesn't necessarily
Beau2016
in
LUPUS UK
12 days ago
Gastroenteritis poo - how long to recover?
I think I've had gastroenteritis. The dr reckons it's led to post infective IBS. I think I had Covid that started it. My poos are like yellow liquid at the mo. Tried live yoghurt today. What is gastroenteritis. poo like? How long did you have it for? What helped?
I think I've had gastroenteritis. The dr reckons it's led to post infective IBS. I think I had Covid that started it. My poos are like yellow liquid at the mo. Tried live yoghurt today. What is gastroenteritis. poo like? How long did you have it for? What helped?
Mackied
in
IBS Network
16 days ago
Ibs bam
Anyone on here have bile acid malabsorption if so wat medication are yous on and do yous get really bad stomach pains even though on medication as I have bam on colesevelam but still get horrible stomach pain I have ibs aswell and docs are saying it's overlapping eachother watever that is supposed to
Anyone on here have bile acid malabsorption if so wat medication are yous on and do yous get really bad stomach pains even though on medication as I have bam on colesevelam but still get horrible stomach pain I have ibs aswell and docs are saying it's overlapping eachother watever that is supposed to
Netbet22
in
IBS Network
18 days ago
Mom Recently Diagnosed 😢 Wondering about Speech Cloning/Voice Banking
Hello everyone. My mom was diagnosed with PSP on May 31st of this year but has been experiencing symptoms for about two and a half years now. She is only 56 and this disease feels unbearable in its cruelty and its early onset. We have been very lucky so far that she still has her speech and personality
Hello everyone. My mom was diagnosed with PSP on May 31st of this year but has been experiencing symptoms for about two and a half years now. She is only 56 and this disease feels unbearable in its cruelty and its early onset. We have been very lucky so far that she still has her speech and personality
ThankfulFish
in
PSP Association
20 days ago
Arrhythmias: Understanding your condition
Arrhythmias are heart rhythm disorders of your heart’s electrical system, whereby there is a change in the regular beat of your heart, causing it to beat irregularly. Sometimes if the conduction pathway is damaged or becomes blocked, or if an extra pathway exists, the heart’s rhythm changes. For more
Arrhythmias are heart rhythm disorders of your heart’s electrical system, whereby there is a change in the regular beat of your heart, causing it to beat irregularly. Sometimes if the conduction pathway is damaged or becomes blocked, or if an extra pathway exists, the heart’s rhythm changes. For more
SamAdmin
Administrator
in
Atrial Fibrillation Support
23 days ago
Arrhythmias: Understanding your condition
Arrhythmias are heart rhythm disorders of your heart’s electrical system, whereby there is a change in the regular beat of your heart, causing it to beat irregularly. Sometimes if the conduction pathway is damaged or becomes blocked, or if an extra pathway exists, the heart’s rhythm changes. For more
Arrhythmias are heart rhythm disorders of your heart’s electrical system, whereby there is a change in the regular beat of your heart, causing it to beat irregularly. Sometimes if the conduction pathway is damaged or becomes blocked, or if an extra pathway exists, the heart’s rhythm changes. For more
SamAdmin
Administrator
in
Heart Rhythm Disorders Support
23 days ago
post ablation pneumonia
twelve days post ablation and I have been back in hospital for four days with a bit of stubborn pneumonia w fluid in lungs. Care is great. Facilities lovely and comfortable, but I am weak and ready to feel well, please. no one seems surprised that I got pneumonia from breathing tube during procedure
twelve days post ablation and I have been back in hospital for four days with a bit of stubborn pneumonia w fluid in lungs. Care is great. Facilities lovely and comfortable, but I am weak and ready to feel well, please. no one seems surprised that I got pneumonia from breathing tube during procedure
37Polly
in
Atrial Fibrillation Support
23 days ago
Shingles Vaccination
Anyone had shingles vaccination while on ADT (Orgovyx and Zytega) ? Any reaction to the first and second dose of the shingles vaccination? THx
Anyone had shingles vaccination while on ADT (Orgovyx and Zytega) ? Any reaction to the first and second dose of the shingles vaccination? THx
Sushupthi
in
Advanced Prostate Cancer
24 days ago
Hepatitis B (HBV) Virtual Support Group – Tuesday 17th September at 6pm (UK)
Do you live with Hep B and are in the UK?
Why not join us later this month for the next Hep B support group? This online session is on Tuesday, 17th September from 6pm to 7pm on Zoom. This is a peer-led discussion with time for you to share things with the group, or ask any questions you
Do you live with Hep B and are in the UK?
Why not join us later this month for the next Hep B support group? This online session is on Tuesday, 17th September from 6pm to 7pm on Zoom. This is a peer-led discussion with time for you to share things with the group, or ask any questions you
BritishLiverTrust1
Partner
in
British Liver Trust
24 days ago
cold medicine
hello, is there a cold medicine that is safe to take with RLS?
hello, is there a cold medicine that is safe to take with RLS?
Haydenpup
in
Restless Legs Syndrome
26 days ago
It's A Mans World : Fibromyalgia/Prostatitis Bad Body Smells
[i]Hyper embarrassing question but my whole body smells like urine constantly.[/i]
[i]I wash 3 times daily & use 48 hour deodorant & I'm smelling like a skunk 🦨 [/i]
[i]My only medication is Buprenorphine 20 mg patches which you have to change every 7 days.[/i]
[i] [/i]
[b
[i]Hyper embarrassing question but my whole body smells like urine constantly.[/i]
[i]I wash 3 times daily & use 48 hour deodorant & I'm smelling like a skunk 🦨 [/i]
[i]My only medication is Buprenorphine 20 mg patches which you have to change every 7 days.[/i]
[i] [/i]
[b
Fibroguy66
in
Fibromyalgia Action UK
28 days ago
1
2
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Lung Conditions Community Forum
2968 results
Fertility Network UK
2869 results
NRAS
2374 results
View top 10 communities
Sort by
Most Relevant
Newest