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Covid outbreak
Well, nearly 6 weeks post transplant, things all stable and improving slowly.....I knew it was too good to be true. And.......My 15yr old son has tested positive for Covid this am.Same old thing weve struggled with all along this journey. We can wrap husband in cotton wool, sheild, stay home, cancel
Well, nearly 6 weeks post transplant, things all stable and improving slowly.....I knew it was too good to be true. And.......My 15yr old son has tested positive for Covid this am.Same old thing weve struggled with all along this journey. We can wrap husband in cotton wool, sheild, stay home, cancel
Ewife
in
British Liver Trust
7 days ago
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
7 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
8 days ago
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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
9 days ago
Hi, new to this page/forum, looking for information and advice.
Have been on PAS page and Thyroid UK page for a few years but just thought I'd be greedy and join yourselves too. Have been having increasing levels of pain and discomfort for years but just told lose weight, take brufen. Last few years have been awful , eventually got a referral to Rheumatology. Bloods
Have been on PAS page and Thyroid UK page for a few years but just thought I'd be greedy and join yourselves too. Have been having increasing levels of pain and discomfort for years but just told lose weight, take brufen. Last few years have been awful , eventually got a referral to Rheumatology. Bloods
Polo22
in
NRAS
10 days ago
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
10 days ago
Steroid injection into Kiloid Scars
I have a dermatology appointment on Saturday (yes an NHS appointment on a Saturday) to review treatment of kiloid scars. I think one of the options suggested may be direct steroid injections into the scars themselves. I have had PMR for 9 years and have at last got stable on 7 mg prednisolone daily
I have a dermatology appointment on Saturday (yes an NHS appointment on a Saturday) to review treatment of kiloid scars. I think one of the options suggested may be direct steroid injections into the scars themselves. I have had PMR for 9 years and have at last got stable on 7 mg prednisolone daily
scrambledegg
in
PMRGCAuk
11 days 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
11 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
11 days 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
13 days 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
13 days 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
14 days 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
15 days 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
15 days ago
Confused
I had my first appointment with an endo specialist today. I think I'm still in shock at the whole situation to be honest and am trying to sort things out in my head. I've just turned 40 and there's no history of endo in my family. I've been diagnosed with endo and adenomyosis. The endo is between
I had my first appointment with an endo specialist today. I think I'm still in shock at the whole situation to be honest and am trying to sort things out in my head. I've just turned 40 and there's no history of endo in my family. I've been diagnosed with endo and adenomyosis. The endo is between
Tulip1983
in
Endometriosis UK
9 months ago
High B12 result.
Hello all you Trusty Advisers, Anyone please able to help give me any idea what these results mean to me? GP fast tracked me for bloods & pelvic scan due to a cpl sml vaginal bleeds/spotting (I'm 67) Results have only just been put on my record but GP not spoken to me regarding it. (Report says Satisfactory
Hello all you Trusty Advisers, Anyone please able to help give me any idea what these results mean to me? GP fast tracked me for bloods & pelvic scan due to a cpl sml vaginal bleeds/spotting (I'm 67) Results have only just been put on my record but GP not spoken to me regarding it. (Report says Satisfactory
Klawd
in
Thyroid UK
9 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
18 days 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
18 days 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
20 days ago
Experience of Covid Vaccines and Adrenals
I know the covid vaccines are a hot topic here. I don’t know if mum’s experience is helpful to share. Last years jabs were both a nightmare - led to weakness, temperature, light headedness loss of mobility and a significant down step in her dementia. Despite being a real advocate for the jabs I was
I know the covid vaccines are a hot topic here. I don’t know if mum’s experience is helpful to share. Last years jabs were both a nightmare - led to weakness, temperature, light headedness loss of mobility and a significant down step in her dementia. Despite being a real advocate for the jabs I was
RT18
in
PMRGCAuk
22 days ago
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