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Covid treatment
Hi all. Has anyone had treatment for Covid recently (since guidelines changed and you don’t automatically get referred). I am Covid positive and really struggling with symptoms. Have recently had treatment for a PE. The called 111 to arrange Covid treatment and they are sending a non urgent ambulance
Hi all. Has anyone had treatment for Covid recently (since guidelines changed and you don’t automatically get referred). I am Covid positive and really struggling with symptoms. Have recently had treatment for a PE. The called 111 to arrange Covid treatment and they are sending a non urgent ambulance
Pink75928
in
NRAS
5 months ago
New valve- but now afib and thinner
female, 49yrs old (almost 50) Ive had an aortic valve, root and ascending aorta replacement 9 months ago. Bovine valve to avoid thinners for a better life. Im still recovering, a was symptomatic too long i think ( 3 years really struggling but a known lifelong long valve leak) … and since the
female, 49yrs old (almost 50) Ive had an aortic valve, root and ascending aorta replacement 9 months ago. Bovine valve to avoid thinners for a better life. Im still recovering, a was symptomatic too long i think ( 3 years really struggling but a known lifelong long valve leak) … and since the
Bebop2023
in
Heart Valve Voice
5 months ago
Update
Hi all. It has been 3 yrs now since my brother came out of ICU and then to a ward and into a home to clear space in Hospital during Covid. Unfortunately his muscles wasted away within a month of being in ICU and the inability to move from the neck down . He is classed as quadrapleagic. His legs have
Hi all. It has been 3 yrs now since my brother came out of ICU and then to a ward and into a home to clear space in Hospital during Covid. Unfortunately his muscles wasted away within a month of being in ICU and the inability to move from the neck down . He is classed as quadrapleagic. His legs have
Twoblu
in
ICUsteps
5 months ago
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Pudendal neuralgia
I believe I have been suffering from PN for over a year. I have seen many doctors and have had nerve blocks with a few hours of relief. i also had pulsed radiofrequency nerve ablation with i day of relief. Recently had bottox and seeing a PT. the PT is all bookeed up and I had to make an appointment
I believe I have been suffering from PN for over a year. I have seen many doctors and have had nerve blocks with a few hours of relief. i also had pulsed radiofrequency nerve ablation with i day of relief. Recently had bottox and seeing a PT. the PT is all bookeed up and I had to make an appointment
shilsenrod
in
Pelvic Pain Support Network
11 months ago
Thrush 3 days before FET
Hi everyone, I am booked for a natural FET on Monday (I didn't take anything this cycle, not even progesterone) and the Friday before I discovered that my discharge looked like cottage cheese and I may be getting thrush. Which I haven't had in years! Has this happened to anyone else before their FET
Hi everyone, I am booked for a natural FET on Monday (I didn't take anything this cycle, not even progesterone) and the Friday before I discovered that my discharge looked like cottage cheese and I may be getting thrush. Which I haven't had in years! Has this happened to anyone else before their FET
raverg
in
Fertility Network UK
3 months ago
Lichenoid Dermatitis
I took a statin drug in January 2023 & by end of Feb 2023 I had skin ddiscolorations. In Mar I went to a dermatologist who started treating me with steroids & by May I had a biopsy, it was Lichenoid Dermatitis. It's left ugly, dark splotches on mmeals over with peeling skin. I'm using Dupixent every
I took a statin drug in January 2023 & by end of Feb 2023 I had skin ddiscolorations. In Mar I went to a dermatologist who started treating me with steroids & by May I had a biopsy, it was Lichenoid Dermatitis. It's left ugly, dark splotches on mmeals over with peeling skin. I'm using Dupixent every
Skywriter0
in
MY SKIN
7 months ago
GCA relief of symptoms?
Hi, help please.I have had a GCA flare, headaches, sore temples, total fatigue, dizzy spells and jaw pain. Rheumatologist appt 20 Sept 2023 increased pred to 40mgs a day for 3 weeks, then reducing. 16 days later though, I still have the symptoms. Does that sound ok? Previously I had been on 3mgs of
Hi, help please.I have had a GCA flare, headaches, sore temples, total fatigue, dizzy spells and jaw pain. Rheumatologist appt 20 Sept 2023 increased pred to 40mgs a day for 3 weeks, then reducing. 16 days later though, I still have the symptoms. Does that sound ok? Previously I had been on 3mgs of
Chespoll
in
PMRGCAuk
7 months ago
new here
Hi everyone, I was signposted to this group by my GP so just sighed up. My T started after having covid. I was diagnosed with long covid this year which has been terribly life altering. I Have not been able to return to my job as a nurse which is sad. I suddenly developed tinnitus in just one ear
Hi everyone, I was signposted to this group by my GP so just sighed up. My T started after having covid. I was diagnosed with long covid this year which has been terribly life altering. I Have not been able to return to my job as a nurse which is sad. I suddenly developed tinnitus in just one ear
Jb2309
in
Tinnitus UK
5 months ago
Back Pain Advice and Meds
Hi I posted this in a different forum as unsure which one to use? Anyhow, for the past 6 months I have had very bad back pain which is impacting daily life. I have no idea what triggered it but my physio says she sees it all the time and it is degenerative disc disease. I have paid for a dozen physio
Hi I posted this in a different forum as unsure which one to use? Anyhow, for the past 6 months I have had very bad back pain which is impacting daily life. I have no idea what triggered it but my physio says she sees it all the time and it is degenerative disc disease. I have paid for a dozen physio
Jo198919
in
Cloudy with a Chance of Pain
5 months ago
Back Pain Medication/Advice
For the past 6 months I have had very bad back pain which is impacting daily life. I have no idea what triggered it but my physio says she sees it all the time and it is degenerative disc disease. I have paid for a dozen physio sessions and several osteopath sessions which have not been helpful unfortunately
For the past 6 months I have had very bad back pain which is impacting daily life. I have no idea what triggered it but my physio says she sees it all the time and it is degenerative disc disease. I have paid for a dozen physio sessions and several osteopath sessions which have not been helpful unfortunately
Jo198919
in
Pain Concern
5 months ago
Very fast onset of Pneumonia! It’s a long story; are you comfortable…
My husband is on W&W for CLL, though he may start treatment soon. Well, he had a heavy cold (as did I) and though it lingered abit we weren’t too concerned. Was still coughing up green mucus abit but he wasn’t concerned (I was and told him but … well, he felt better he said) Day before Christmas Eve
My husband is on W&W for CLL, though he may start treatment soon. Well, he had a heavy cold (as did I) and though it lingered abit we weren’t too concerned. Was still coughing up green mucus abit but he wasn’t concerned (I was and told him but … well, he felt better he said) Day before Christmas Eve
Tpdnotts
in
CLL Support
4 months ago
Side effects of Buprenorphine
Several persons on this site have already helped me but I want to ask the general following about the use of Buprenorphine for treatment of RLS. and its augmentation After testing in vain, pregabalin, oxycodone several other less well advertised RLS treatments I got agreement from my GP to try Buprenorphine
Several persons on this site have already helped me but I want to ask the general following about the use of Buprenorphine for treatment of RLS. and its augmentation After testing in vain, pregabalin, oxycodone several other less well advertised RLS treatments I got agreement from my GP to try Buprenorphine
davchar23
in
Restless Legs Syndrome
3 months ago
Anxiety or hormones?
I've been feeling light headed and off balance since being diagnosed hypothyroid years ago, could be meds side effects or the gland itself. I'm also post menopausal so low oestrogen. Allergies bung up the eustachian tunes cause imbalance. All of these can cause disequilibrium leading to anxiety. I had
I've been feeling light headed and off balance since being diagnosed hypothyroid years ago, could be meds side effects or the gland itself. I'm also post menopausal so low oestrogen. Allergies bung up the eustachian tunes cause imbalance. All of these can cause disequilibrium leading to anxiety. I had
celticlady
in
Anxiety Support
5 months ago
Finally got an endocrinology appointment
Hi there everyone!In early January this year I caught COVID and was really rough with it even though I have had all my jabs, come February I was still feeling rough, tired, always cold, brain fog... The list goes on. I went to the GP and explained my symptoms but didn't say I'd had COVID (expecting
Hi there everyone!In early January this year I caught COVID and was really rough with it even though I have had all my jabs, come February I was still feeling rough, tired, always cold, brain fog... The list goes on. I went to the GP and explained my symptoms but didn't say I'd had COVID (expecting
unlucky-angler
in
Thyroid UK
5 months ago
Covid and Blood Tests
Hello lovely people. I wasn't given the jab this year and I've recently had a pretty bad dose of Covid (four days of fever at 102, oxygen sats down to 92% at one point) and my heart rate went crazy and I had one episode of SVT briefly the first time I got out of bed after the fever. Only one, mind
Hello lovely people. I wasn't given the jab this year and I've recently had a pretty bad dose of Covid (four days of fever at 102, oxygen sats down to 92% at one point) and my heart rate went crazy and I had one episode of SVT briefly the first time I got out of bed after the fever. Only one, mind
SilverSavvy
in
Thyroid UK
5 months ago
I'm really tired with all these ideas about lung cancer
I was diagnosed with pneumonia, I don't know what stage of pneumonia I have, it was not mentioned in the x-ray results. The results were sent to my GP, and he prescribed me medications to treat pneumonia. I think it is difficult to know what stage I have, even if I thought about this. This is because
I was diagnosed with pneumonia, I don't know what stage of pneumonia I have, it was not mentioned in the x-ray results. The results were sent to my GP, and he prescribed me medications to treat pneumonia. I think it is difficult to know what stage I have, even if I thought about this. This is because
Vinaa
in
Lung Conditions Community Forum
4 months ago
Vaccine disparities are worse post-emergency KATELYN JETELINA NOV 28 Data is starting to roll in on Covid-19 vaccine inequities this fall
Vaccine disparities are worse post-emergency KATELYN JETELINA NOV 28 https://yourlocalepidemiologist.substack.com/p/vaccine-disparities-are-worse-post?utm_source=post-email-title&publication_id=281219&post_id=139105358&utm_campaign=email-post-title&isFreemail=true&r=dr96q&utm_medium=email - Oof.
Vaccine disparities are worse post-emergency KATELYN JETELINA NOV 28 https://yourlocalepidemiologist.substack.com/p/vaccine-disparities-are-worse-post?utm_source=post-email-title&publication_id=281219&post_id=139105358&utm_campaign=email-post-title&isFreemail=true&r=dr96q&utm_medium=email - Oof.
lankisterguy
Volunteer
in
CLL Support
5 months ago
Shingles and MTX
I'm due to go visit family but brother-in-law has shingles. Normally I wouldn't worry as I have had chicken pox but the NHS in advice on taking MTX says to contact the doctor if you've been exposed to shingles (which suggests we should avoid contact with shingles patients). Has anyone been advised to
I'm due to go visit family but brother-in-law has shingles. Normally I wouldn't worry as I have had chicken pox but the NHS in advice on taking MTX says to contact the doctor if you've been exposed to shingles (which suggests we should avoid contact with shingles patients). Has anyone been advised to
Gottarelax
in
NRAS
7 months ago
Alvesco and fostair
I am currently on fostair 100 mart, with the ability to switch to fostair 200 when I need it. Along with spiriva. My asthma is relatively uncontrolled, but spiriva has helped a lot. My consultant has just put Alvesco 160 into the mix twice a day. Any idea of what he is doing, apart from just increasing
I am currently on fostair 100 mart, with the ability to switch to fostair 200 when I need it. Along with spiriva. My asthma is relatively uncontrolled, but spiriva has helped a lot. My consultant has just put Alvesco 160 into the mix twice a day. Any idea of what he is doing, apart from just increasing
Homely2
Administrator
in
Asthma Community Forum
7 months ago
still not diagnosed but concerned about IBS
Sorry for lengthy post I am new here. I started an antibiotics course (one week) Doxycycline on 24 April 2023 for throat infection and fever,as soon I finish it, I started having diarrhoea. That time I was in very stress and depression for another reason. It's been almost over 9 months now. Diarrhea
Sorry for lengthy post I am new here. I started an antibiotics course (one week) Doxycycline on 24 April 2023 for throat infection and fever,as soon I finish it, I started having diarrhoea. That time I was in very stress and depression for another reason. It's been almost over 9 months now. Diarrhea
Fmkhan
in
IBS Network
7 months ago
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