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Tinnitus getting louder everyday, I am scared
I have had tinnitus for 3 years. It started of with one ringing tone and I habituated straight away. It started to get louder with a white noise, some[point over the years, 2 weeks later I got use to it again. But I had a ear infection, covid and (last few weeks) and since then have several tones
I have had tinnitus for 3 years. It started of with one ringing tone and I habituated straight away. It started to get louder with a white noise, some[point over the years, 2 weeks later I got use to it again. But I had a ear infection, covid and (last few weeks) and since then have several tones
lifeseeker
in
Tinnitus UK
26 days ago
Ra spring Covid vac
has anyone had side effects from spring Covid omicron spike vax I’ve not stopped sneezing since had booster one week ago.
has anyone had side effects from spring Covid omicron spike vax I’ve not stopped sneezing since had booster one week ago.
Passionflower
in
NRAS
26 days ago
Monoclonal antibody infusion for covid?
I'm on Zepatier for Hep C. Managed to get a very nasty case of pneumonia just after starting that and was hospitalised including ICU for 10 days. I've been out of hospital for 6 weeks now and was starting to feel better. Then I came down with what I thought was a cold earlier this week and I tested positive
I'm on Zepatier for Hep C. Managed to get a very nasty case of pneumonia just after starting that and was hospitalised including ICU for 10 days. I've been out of hospital for 6 weeks now and was starting to feel better. Then I came down with what I thought was a cold earlier this week and I tested positive
NieceByMarriage
in
British Liver Trust
27 days ago
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Mental health?
I developed EPI after having Covid. In August of 2021. My fist attempt at eating after my fever broke sent my to the emergency room with sever pain. At the time they suspected pancreatitis, but because I was still recovering from covid they ran other tests, told me I had covid pneumonia and sent me home
I developed EPI after having Covid. In August of 2021. My fist attempt at eating after my fever broke sent my to the emergency room with sever pain. At the time they suspected pancreatitis, but because I was still recovering from covid they ran other tests, told me I had covid pneumonia and sent me home
Ethelknows
in
Chronic Pancreatitis Support
28 days ago
PID abcess laposcopy adhesiolysis
In November I had severe pelvic pain and back pain and I went to my GP where they said they suspected I had kidney stones. That evening the pain was so severe my Husband called 999 who told him to take me to A&E. There again I was sent home shortly after saying I was fine, and they booked me in for a
In November I had severe pelvic pain and back pain and I went to my GP where they said they suspected I had kidney stones. That evening the pain was so severe my Husband called 999 who told him to take me to A&E. There again I was sent home shortly after saying I was fine, and they booked me in for a
Busy23
in
Pelvic Pain Support Network
5 months ago
Covid and lung cancer
My husband has Covid and so far I'm not showing any symptoms, but I'm concerned about how it might affect someone with lung cancer. Any advice welcome. I'm being very careful, wearing a mask My husband is banished to the upstairs TV or the other end of the garden to avoid contact ! I've never
My husband has Covid and so far I'm not showing any symptoms, but I'm concerned about how it might affect someone with lung cancer. Any advice welcome. I'm being very careful, wearing a mask My husband is banished to the upstairs TV or the other end of the garden to avoid contact ! I've never
Gingergus
in
The Roy Castle Lung Cancer Foundation
29 days ago
New here looking for some help!
Hi all. I’ve just found this forum as I’ve been lokkkng for help for quite some time. I’ve had the weirdest thing happen…… Bit of a back story first…..I never had asthma my entire life. Until I got COVID for the first time in August 2021. I was considered high risk as it was as I also have rheumatoid
Hi all. I’ve just found this forum as I’ve been lokkkng for help for quite some time. I’ve had the weirdest thing happen…… Bit of a back story first…..I never had asthma my entire life. Until I got COVID for the first time in August 2021. I was considered high risk as it was as I also have rheumatoid
Gonewiththewindddddd
in
Asthma Community Forum
29 days ago
I’m scheduled to have DBS surgery February 29 - if you have had DBS, is there anything you wish you‘d known beforehand?
I want to prepare mentally (and physically) for the surgery, and would appreciate any input from members of this community who have had the experience of DBS surgery. Thank you in advance. Wayne
I want to prepare mentally (and physically) for the surgery, and would appreciate any input from members of this community who have had the experience of DBS surgery. Thank you in advance. Wayne
Megafone
in
Cure Parkinson's
6 months ago
Good news/bad news
hi all. The nurse rang last week to say that my liver results had improved somewhat but were still outside normal range. Because I have such active disease she didn’t want to leave me with no meds at all, so we decided to restart the leflunomide and see how the blood results go in two week, then make
hi all. The nurse rang last week to say that my liver results had improved somewhat but were still outside normal range. Because I have such active disease she didn’t want to leave me with no meds at all, so we decided to restart the leflunomide and see how the blood results go in two week, then make
HeadInASpin
in
NRAS
1 month ago
Post covid oxygen levels.
Hi, I have recently had covid which left me with a dreadful COPD exacerbation. I was given anti virals and taken rescue pack followed by another course of Doxycycline. Although I feel a lot better my oxygen levels have dropped dreadfully. I am prescribed ambulatory oxygen but am finding I am using it
Hi, I have recently had covid which left me with a dreadful COPD exacerbation. I was given anti virals and taken rescue pack followed by another course of Doxycycline. Although I feel a lot better my oxygen levels have dropped dreadfully. I am prescribed ambulatory oxygen but am finding I am using it
Maggity
in
Lung Conditions Community Forum
1 month ago
Dreaded Covid
Having started with a bad cold last week after having a gastroscope, at my local hospital, I didn’t think too much about it at first, eventually went to doctors said it was a virus and chest was clear just drink plenty fluids, then my daughter thought best check covid and it was positive, can’t hear
Having started with a bad cold last week after having a gastroscope, at my local hospital, I didn’t think too much about it at first, eventually went to doctors said it was a virus and chest was clear just drink plenty fluids, then my daughter thought best check covid and it was positive, can’t hear
Alibongo60
in
Headway
1 month ago
clonazepam lethargy
has anyone experienced extreme fatigue since taking Clonazepam. My husband has been taking this now for around 10 days. He seems to be sleeping better at night but extremely tired during the day and i think this might be impacting his ability to walk as he can barely stand up without falling backwards
has anyone experienced extreme fatigue since taking Clonazepam. My husband has been taking this now for around 10 days. He seems to be sleeping better at night but extremely tired during the day and i think this might be impacting his ability to walk as he can barely stand up without falling backwards
Licquoricelover
in
PSP Association
1 month ago
MSK Community Care
Hello All Just had my latest check up at the Hospital. After a terrible flare about a year and a half ago, which took ages to get under control, Sulfa was finally added to my Mthx and has really been a game changer. I have also been lucky enough to have an absolutely amazing Rheumatologist and I have
Hello All Just had my latest check up at the Hospital. After a terrible flare about a year and a half ago, which took ages to get under control, Sulfa was finally added to my Mthx and has really been a game changer. I have also been lucky enough to have an absolutely amazing Rheumatologist and I have
Chockyuk
in
NRAS
2 months ago
covid related?
does anyone feel ike the tinnitus started after covid? Just interested in any links, I’ve recently had a bad virus not tested for covid but it was quite nasty and I’m wondering if that’s why my tinnitus is worse
does anyone feel ike the tinnitus started after covid? Just interested in any links, I’ve recently had a bad virus not tested for covid but it was quite nasty and I’m wondering if that’s why my tinnitus is worse
Retailgirl
in
Tinnitus UK
1 month ago
I’m Back
it has been quite a while since I have been on this message board, life just happens as we all know with Lupus. Many changes have occurred from multifocal, pneumonia, aspergillus in my lung and tumor in my lung upper right lobe… however, it is benign right now and they’re just going to watch it. I
it has been quite a while since I have been on this message board, life just happens as we all know with Lupus. Many changes have occurred from multifocal, pneumonia, aspergillus in my lung and tumor in my lung upper right lobe… however, it is benign right now and they’re just going to watch it. I
SunflowerYiayia
in
LUPUS UK
5 months ago
How do you get diagnosed on the NHS
Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand
Hello all. I've just joined this forum and have a bit of a perplexing question. For years I've suffered from food intolerances and mild allergies. I have had (and still have) various autoimmune issues. Post Covid in 2020, I developed hay fever along with an increasing number of food intolerances qand
Treetop33
in
The UK Mastocytosis Support Group
1 month ago
Covid, covid test and tapering
Very slow tapering (DL style and working well) currently at 5mg prednisolone. Just into my 3rd year PMR diagnosis, when I contracted covid. Staying put at 5 mg now. PMR bouts of fatigue and sleepiness much worse this time though just starting to improve a little. not the case on my previous covid infection
Very slow tapering (DL style and working well) currently at 5mg prednisolone. Just into my 3rd year PMR diagnosis, when I contracted covid. Staying put at 5 mg now. PMR bouts of fatigue and sleepiness much worse this time though just starting to improve a little. not the case on my previous covid infection
waltztherapy
in
PMRGCAuk
1 month ago
Kinder , Gentler and harmless Alternative of DBS
Seeking a kinder, gentler alternative, researchers from Korea's Yonsei University created minuscule magnets tagged with antibodies. The devices are known as nanoscale magnetic force actuators, or m-Torquers. These m-Torquers were injected into the subthalamic nucleus of mice with early- and late-stage
Seeking a kinder, gentler alternative, researchers from Korea's Yonsei University created minuscule magnets tagged with antibodies. The devices are known as nanoscale magnetic force actuators, or m-Torquers. These m-Torquers were injected into the subthalamic nucleus of mice with early- and late-stage
Farooqji
in
Cure Parkinson's
6 months ago
psoriasis flair and adalimumab
hi all, I am looking for some advice. I had severe psoriasis which was almost gone thanks to adalimumab. I saw my dermatology team back in April for my 6 monthly check where my psoriasis was flairing up. so I had an adalimumab blood test to see if it was meant to work. I got the results back a
hi all, I am looking for some advice. I had severe psoriasis which was almost gone thanks to adalimumab. I saw my dermatology team back in April for my 6 monthly check where my psoriasis was flairing up. so I had an adalimumab blood test to see if it was meant to work. I got the results back a
katienewland
in
Beyond Psoriasis
1 month ago
GCA flare
Diagnosed April 2018 with PMR. Three months later GCA. I am currently on 3mgs prednisolone. Over the last two days have scalp pain on right side only … no jaw pain. It feels a bit like I am getting a cold sore but no cold sore showing up. Could it be a GCA flare? Thank you to everyone who replies.
Diagnosed April 2018 with PMR. Three months later GCA. I am currently on 3mgs prednisolone. Over the last two days have scalp pain on right side only … no jaw pain. It feels a bit like I am getting a cold sore but no cold sore showing up. Could it be a GCA flare? Thank you to everyone who replies.
Reddev
in
PMRGCAuk
10 months ago
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