Search
Search
About
Log in
Join
Experiences with
Nerve or brain infections
Posts
Communities
31,395 public posts
Filter results
My our Journey so far.
A BIG Hi to you all. I’d like to introduce myself. My nick name is Big H and my journey started in 2021 with a covid pneumonia. I was in a pub when we were allowed to go out, it’s the only place I had attended before contracting Covid Pneumonia. I just remember it was like having the worse flu and
A BIG Hi to you all. I’d like to introduce myself. My nick name is Big H and my journey started in 2021 with a covid pneumonia. I was in a pub when we were allowed to go out, it’s the only place I had attended before contracting Covid Pneumonia. I just remember it was like having the worse flu and
BigH63
in
ICUsteps
10 months ago
T since Covid
My T started just after I had Covid . It is up and down in volume but every day. Have any others on here had T since Covid and still have it. Andy
My T started just after I had Covid . It is up and down in volume but every day. Have any others on here had T since Covid and still have it. Andy
Andy4713
in
Tinnitus UK
9 months ago
UTI/bladder issues/pain
This article is an interesting read… https://www.medicalnewstoday.com/articles/overactive-bladder-thyroid Especially as of a lately iv been struggling with my bladder, and a UTI, the UTI cleared up with antibiotics (which nearly killed me off!) but now certain foods/drinks trigger bladder pain!? I
This article is an interesting read… https://www.medicalnewstoday.com/articles/overactive-bladder-thyroid Especially as of a lately iv been struggling with my bladder, and a UTI, the UTI cleared up with antibiotics (which nearly killed me off!) but now certain foods/drinks trigger bladder pain!? I
ThyroidObsessed
in
Thyroid UK
9 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
stiffness
Hi I have read that people experience lot of stiffness with PMR , especially in the mornings . However , I never do , maybe slightly for a few mins. GPS say I do have pmr. My inflammation levels were 39 in the spring . I was given 40mg steroids per day , as suspected GCA . Then saw a rheumy who
Hi I have read that people experience lot of stiffness with PMR , especially in the mornings . However , I never do , maybe slightly for a few mins. GPS say I do have pmr. My inflammation levels were 39 in the spring . I was given 40mg steroids per day , as suspected GCA . Then saw a rheumy who
TedTheMaineCoon
in
PMRGCAuk
9 months ago
Propafenone and taste
Anyone have any firsthand experience with Propafenone and taste? Everything tastes disgusting this morning and I hope its a side effect that fades.😬. Still not convinced it is going to even stop the Atrial Tachycardia as I am still having it, but now this.... Ugh.
Anyone have any firsthand experience with Propafenone and taste? Everything tastes disgusting this morning and I hope its a side effect that fades.😬. Still not convinced it is going to even stop the Atrial Tachycardia as I am still having it, but now this.... Ugh.
MeganMN
in
AF Association
10 months ago
Metratrexate injection
hi all! I’m due my weekly metratrexate injection tomorrow but I have a little sniffle nothing much as yet but think I could be getting a cold..my question is do people that are on metratrexate still have it with a sniffle/cold ? I haven’t had a cold since starting the metratrexate that’s why I’m asking
hi all! I’m due my weekly metratrexate injection tomorrow but I have a little sniffle nothing much as yet but think I could be getting a cold..my question is do people that are on metratrexate still have it with a sniffle/cold ? I haven’t had a cold since starting the metratrexate that’s why I’m asking
Mybirthday1975
in
NRAS
6 months ago
4dp5dt and have cold/flu
so I’m just being majorly paranoid and looking for reassurance as yesterday I started developing a cold that seems more like the flu now. Now just overthinking things being like it definitely won’t work now 😳 anyone else managed to get a positive despite this happening or got any stories of reassurance
so I’m just being majorly paranoid and looking for reassurance as yesterday I started developing a cold that seems more like the flu now. Now just overthinking things being like it definitely won’t work now 😳 anyone else managed to get a positive despite this happening or got any stories of reassurance
Cutecolliedog
in
Fertility Network UK
6 months ago
update on knee pain
As most of you will probably know, I injured my knee on holiday at the end of June, when my knee would buckle. Over the months Drs have always been more concerned that my back or pelvis was injured with a fall in the shower, due to the knee buckling. I had CT scans and MRIof the spine and pelvis, but
As most of you will probably know, I injured my knee on holiday at the end of June, when my knee would buckle. Over the months Drs have always been more concerned that my back or pelvis was injured with a fall in the shower, due to the knee buckling. I had CT scans and MRIof the spine and pelvis, but
Runrig01
in
NRAS
9 months ago
Postnasal Drip
Help everybody again! Doctor being really unhelpful. I still have this horrendous post nasal drip that finally I have discovered by going private to an ENT chap is silent reflux. I am having an Ensoscopy on Friday to determine it is my Hyitas Hernia playing up. In the meantime my post nasal drip has
Help everybody again! Doctor being really unhelpful. I still have this horrendous post nasal drip that finally I have discovered by going private to an ENT chap is silent reflux. I am having an Ensoscopy on Friday to determine it is my Hyitas Hernia playing up. In the meantime my post nasal drip has
Bronchiectasislady69
in
Lung Conditions Community Forum
9 months ago
Does TENS machines help with Endometriosis?
I am willing to trial anything if it will help reduce my symptoms as I'm struggling quite badly. Someone told me to get a TENS machine as it could help with the pain I've been having. I'm just wondering if anyone has had any experience with this or have tried it and it helps with there endo pain?
I am willing to trial anything if it will help reduce my symptoms as I'm struggling quite badly. Someone told me to get a TENS machine as it could help with the pain I've been having. I'm just wondering if anyone has had any experience with this or have tried it and it helps with there endo pain?
LilacPetals
in
Endometriosis UK
9 months ago
tinnitus - get your hearing aids insured!!
while out on a regular five mile hill walk two weeks ago high up on the Quantocks, with the weather windy and cold then warmer and still, my hat was on and off every ten mins. By the time I reached the car I noticed that one of the aids was no longer there. It’s wasnt in the scarf, down my top or in
while out on a regular five mile hill walk two weeks ago high up on the Quantocks, with the weather windy and cold then warmer and still, my hat was on and off every ten mins. By the time I reached the car I noticed that one of the aids was no longer there. It’s wasnt in the scarf, down my top or in
Bridiecat
in
Tinnitus UK
3 months ago
update on prolotherapy
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
Hidden
in
Neuropathy Support
9 months ago
update on prolotherapy and llltherapy
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
I have had my first prolotherapy injections, they don't hurt much at all.......I must admit the next day I thought oh no I have done the wrong thing....my legs were so bad I wanted to jump off the bridge. Today they have settled down a bit. I suppose this has happened because the prolotherapy causes
Hidden
in
Restless Legs Syndrome
9 months ago
COVID Vaccination and Chest pain
Is anyone out there concerned that there might be a link between COVID booster vaccinations and chest pain. I've posted before about my condition but here's a recap - In December 21, about 10 days after a Pfizer booster, I started to develop chest pain at rest and a burning sensation down my left arm
Is anyone out there concerned that there might be a link between COVID booster vaccinations and chest pain. I've posted before about my condition but here's a recap - In December 21, about 10 days after a Pfizer booster, I started to develop chest pain at rest and a burning sensation down my left arm
Acapella
in
British Heart Foundation
9 months ago
Covid exposure at 8 weeks 3 days pregnant
I'm looking for some reassurance or support. I was in contact with my 9 year old nephew yesterday. He had no symptoms but we spent a good length of time in same room together watching TV with minimal ventilation. Last night he got up with a fever and tested positive for covid on an LFT this morning.
I'm looking for some reassurance or support. I was in contact with my 9 year old nephew yesterday. He had no symptoms but we spent a good length of time in same room together watching TV with minimal ventilation. Last night he got up with a fever and tested positive for covid on an LFT this morning.
SMBCnewbie
in
Fertility Network UK - Pregnancy Support
9 months ago
shingles
I was diagnosed with PMR 3 years ago and after a fairly bumpy ride I have now been off Prednisone for two and a half months. I have been called for a Shingles vaccination. I reacted badly to the Covid jabs each time. I have had Shingles twice! Once about 35 years ago and then for the second time
I was diagnosed with PMR 3 years ago and after a fairly bumpy ride I have now been off Prednisone for two and a half months. I have been called for a Shingles vaccination. I reacted badly to the Covid jabs each time. I have had Shingles twice! Once about 35 years ago and then for the second time
Oldfogie
in
PMRGCAuk
10 months ago
Covid vaccines and Lupus Flare - up
Everytime I get a Covid shot I get a painful Lupus Flare- up for 4 to 5 months . In the 30 years of having Lupus I have never been so sick as since I have been taking Covid shots . I am thinking I will wait at least 1 year , if not longer for another one .
Everytime I get a Covid shot I get a painful Lupus Flare- up for 4 to 5 months . In the 30 years of having Lupus I have never been so sick as since I have been taking Covid shots . I am thinking I will wait at least 1 year , if not longer for another one .
seabreezegirl
in
LUpus Patients Understanding and Support
9 months ago
latest Covid vaccine
Has anyone received conflicting messages about whether or not to get the latest vaccine? My husband asked his primary nephrologist and he told him to just get the flu vaccine, then later he told him to get the Covid vaccine if he’s going to be traveling. This is the doctor who has previously told my
Has anyone received conflicting messages about whether or not to get the latest vaccine? My husband asked his primary nephrologist and he told him to just get the flu vaccine, then later he told him to get the Covid vaccine if he’s going to be traveling. This is the doctor who has previously told my
sugabear
in
Kidney Transplant
9 months ago
Covid and flu vaccination ?
Tomorrow I am due for both a covid and flu vaccination. I received a letter from the health authorities and I was offered both as I have the relevant health issues. This is the first time I fall in this category, even when taking pred. and being in the hospital for 5 days with asthma attack (covid) in
Tomorrow I am due for both a covid and flu vaccination. I received a letter from the health authorities and I was offered both as I have the relevant health issues. This is the first time I fall in this category, even when taking pred. and being in the hospital for 5 days with asthma attack (covid) in
krillemy
in
PMRGCAuk
9 months ago
Hypo with CKD & Bradycardia
Him A little about me, 55, female, psoriatic arthritis from a child, treated with biological Cosentxy and Methotrexate. Fatigue/weight gain led to a diagnosis of Fibromyalgia in 2018 after gallbladder removal. I was treated with high dose steroid injections. Over the next 18 months I suffered 12
Him A little about me, 55, female, psoriatic arthritis from a child, treated with biological Cosentxy and Methotrexate. Fatigue/weight gain led to a diagnosis of Fibromyalgia in 2018 after gallbladder removal. I was treated with high dose steroid injections. Over the next 18 months I suffered 12
SimbaT
in
Thyroid UK
9 months ago
1
...
63
64
65
...
100
Next page
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Lung Conditions Community Forum
2973 results
Fertility Network UK
2834 results
NRAS
2406 results
View top 10 communities
Sort by
Most Relevant
Newest