Search
Search
About
Log in
Join
Experiences with
Hookworm infection
Read more...
Posts
Communities
28,481 public posts
Filter results
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
4 days ago
Exercise and PMR
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
Indigo2417
in
PMRGCAuk
7 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
9 days ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
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
11 days ago
QoL-Lick the spoon
This is an IF, WHEN and NOW thought process. I know many of you have already been through this stage because of your cancer but a few people ( new members and a few regulars) haven’t embraced these ideas. How many of you have probably said to yourself IF this treatment works we’re going to go on a
This is an IF, WHEN and NOW thought process. I know many of you have already been through this stage because of your cancer but a few people ( new members and a few regulars) haven’t embraced these ideas. How many of you have probably said to yourself IF this treatment works we’re going to go on a
MouseAddams
in
Advanced Prostate Cancer
7 months ago
Covid & dosing
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
amala57
in
Thyroid UK
7 months ago
Have COVID - should I get Paxlovid/
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
Lambo1
in
CLL Support
7 months 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
3 months ago
slightly anxious and just looking for moral support
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Abcd123455
in
PMRGCAuk
6 months ago
Starting Pegasys soon
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
IsabelleHo
in
MPN Voice
6 months ago
Natural cycle FET likely to be cancelled due to ovulation on small follicle. What does this mean about my eggs/ ovaries? Having a wobble
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Minniemouse88
in
Fertility Network UK
7 months ago
Covid, strange beast.
I find Covid a bizarre virus. I have had 3 times , hospitalised once. I am in remission after stage 4 diagnosis in 2020. My wife last returned from a company business meeting in Malta attended by 500 employees. She and many of her work mates now in bed with Covid. This is the 4th time my wife has had
I find Covid a bizarre virus. I have had 3 times , hospitalised once. I am in remission after stage 4 diagnosis in 2020. My wife last returned from a company business meeting in Malta attended by 500 employees. She and many of her work mates now in bed with Covid. This is the 4th time my wife has had
stevesmith1964
in
CLL Support
8 months ago
Fod Map Diet
Good morning have been on Fodmap diet since March . Has been getting less strict as I eat some dairy but my diet is generally getting more and more restricted.Im also a Pescatarian and feel that I aren’t getting enough protein or variation . Main Symptoms are Anxiety,dizziness,tinnitus,Nausea,wind
Good morning have been on Fodmap diet since March . Has been getting less strict as I eat some dairy but my diet is generally getting more and more restricted.Im also a Pescatarian and feel that I aren’t getting enough protein or variation . Main Symptoms are Anxiety,dizziness,tinnitus,Nausea,wind
Imisspizza
in
IBS Network
8 months 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)
3 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
3 months ago
Afib worse since Ablation
I had Covid in Oct 2022. I was 57 at the time and in really great shape. I exercise everyday, average about 15,000 steps a day and fast 2 to 3 days a week. As my Covid was winding down and I was feeling better I started having Afib Episodes for the first time in my life. They started off
I had Covid in Oct 2022. I was 57 at the time and in really great shape. I exercise everyday, average about 15,000 steps a day and fast 2 to 3 days a week. As my Covid was winding down and I was feeling better I started having Afib Episodes for the first time in my life. They started off
filmguy5
in
AF Association
8 months ago
What to do after prednisolone rescue ended?
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Merryroundabout
in
Asthma Community Forum
6 months ago
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
Very interesting article: [u]
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
[/u]
2024
https://www.gilmorehealth.com/tetanus-vaccine-decreases-incidence-of-parkinsons-disease-and-slows-its-progression/ It is based on this paper: [u]
Tetanus vaccination
Very interesting article: [u]
Tetanus Vaccine Decreases Incidence of Parkinson’s Disease and Slows Its Progression
[/u]
2024
https://www.gilmorehealth.com/tetanus-vaccine-decreases-incidence-of-parkinsons-disease-and-slows-its-progression/ It is based on this paper: [u]
Tetanus vaccination
Bolt_Upright
in
Cure Parkinson's
1 month ago
Adrenal crisis or flare ?
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday
Cyclo5
in
Thyroid UK
8 months ago
Adrenal Crisis or a Flare?
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday afternoon
Evening all, I've been a casual observer for many months now - my PMR was 'gone' (ie in remission/on holiday/not troubling me) and I had adjusted to Adrenal Insufficiency and a likely permanent dose of Hydrocortisone and Vitamin D. I recovered from a dose of covid about 3 weeks ago. On Saturday afternoon
Cyclo5
in
PMRGCAuk
8 months ago
1
...
29
30
31
...
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
2939 results
Fertility Network UK
2870 results
NRAS
2344 results
View top 10 communities
Sort by
Most Relevant
Newest