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pain after injection
Hi just a bit of advice please. Having a flare at the moment had a steroid injection in my buttock. I’m still hurting 🤕 is it ok to still take Naproxen/ Diclofenac ? Would appreciate any help thanks!
Hi just a bit of advice please. Having a flare at the moment had a steroid injection in my buttock. I’m still hurting 🤕 is it ok to still take Naproxen/ Diclofenac ? Would appreciate any help thanks!
Swanfull
in
NRAS
1 year ago
covid jab
Anyone over 65 , carers,care homes, clinical risk groups,can easily book their covid jab via NHS app/ NHS online or by calling 119 therefore many Gp surgeries are not sending reminders. Had mine yesterday got a next day appointment. Feeling a little rough today mind you, but happened the last time I
Anyone over 65 , carers,care homes, clinical risk groups,can easily book their covid jab via NHS app/ NHS online or by calling 119 therefore many Gp surgeries are not sending reminders. Had mine yesterday got a next day appointment. Feeling a little rough today mind you, but happened the last time I
Kristicats
in
Lung Conditions Community Forum
1 year ago
flu shot
I got the flu shot a month ago and I can barely move my arm it’s so painful
I got the flu shot a month ago and I can barely move my arm it’s so painful
Joanecindy
in
PMRGCAuk
10 months ago
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5dp5dt tww
Hiya anyone on their 2 week wait ? Am 5 days in test date is 5th of march and today had a break down and cried , I have been so crampy past 4 days , today was okay untill abit later in afternoon I just feel so bloated 😫 and heavy in my lower abdomen anyone go on to have a positive? I feel like my AF
Hiya anyone on their 2 week wait ? Am 5 days in test date is 5th of march and today had a break down and cried , I have been so crampy past 4 days , today was okay untill abit later in afternoon I just feel so bloated 😫 and heavy in my lower abdomen anyone go on to have a positive? I feel like my AF
Embo2017
in
Fertility Network UK
7 months ago
flu and covid vaccinations and back pain
Had both this morning - my flu arm is really sore, covid arm is fine, but my back is aching horribly. Could it be connected?
Had both this morning - my flu arm is really sore, covid arm is fine, but my back is aching horribly. Could it be connected?
Nuthatch
in
Bone Health and Osteoporosis UK
1 year ago
covid
Hi I have Lupus plus another couple of auto immune disorders. My question is to anyone who has had Covid. I’m on my 14th day positive. How long has anyone else tested positive for. Thankyou
Hi I have Lupus plus another couple of auto immune disorders. My question is to anyone who has had Covid. I’m on my 14th day positive. How long has anyone else tested positive for. Thankyou
Tregarron
in
LUPUS UK
1 year ago
Is it Asthma COPD or Anxiety?
Hi first time posting and I apologise for the length of my question/information. In May hubby and me both came down with Covid, both had cold like symptoms cough, no smell or taste etc hubby slept a lot I didn’t. After 10 days hubby ok I wasn’t, breathing was difficult and cough horrendous Dr gave
Hi first time posting and I apologise for the length of my question/information. In May hubby and me both came down with Covid, both had cold like symptoms cough, no smell or taste etc hubby slept a lot I didn’t. After 10 days hubby ok I wasn’t, breathing was difficult and cough horrendous Dr gave
Grandmatoboys
in
Asthma Community Forum
1 year ago
Covid booster vaccination : Graves Disease
Any thoughts pl re having the covid booster vaccination when diagnosed with Graves Disease. I have at age 65 Graves Disease - diagnosed June 2023 - latest bloods - TSH/ T3/T4 in range - so improved, weight increasing ( I became under weight by far!) , and other aspects improving / energy a
Any thoughts pl re having the covid booster vaccination when diagnosed with Graves Disease. I have at age 65 Graves Disease - diagnosed June 2023 - latest bloods - TSH/ T3/T4 in range - so improved, weight increasing ( I became under weight by far!) , and other aspects improving / energy a
Littlefoot1thyroiduk
in
Thyroid UK
1 year ago
After covid flare up
after i got covid….just stuffy nose nothing more for 5,6 days…my arthritys flare up!! By back is coming back hurt a lot, even if i am in bio hyrimoz. Anybody have experience that? Suggestions? Tanks
after i got covid….just stuffy nose nothing more for 5,6 days…my arthritys flare up!! By back is coming back hurt a lot, even if i am in bio hyrimoz. Anybody have experience that? Suggestions? Tanks
Jack72
in
NRAS
1 year ago
AIH links to Covid vaccine?
I have been doing research as you do for better or worse when you are newly diagnosed in my case AIH I came across Covid linked articles What are people’s thoughts
I have been doing research as you do for better or worse when you are newly diagnosed in my case AIH I came across Covid linked articles What are people’s thoughts
DebbyJ1
in
British Liver Trust
1 year ago
Success stories - what made all the difference?
hello! I’m currently in the middle of my 2nd fresh ICSI cycle (pre-egg collection) and in need of some positivity and inspiration. I’m hoping this will also help others feeling a bit defeated too. If you have had success with IVF/ICSI, please could you share any tips? What do you think made all the
hello! I’m currently in the middle of my 2nd fresh ICSI cycle (pre-egg collection) and in need of some positivity and inspiration. I’m hoping this will also help others feeling a bit defeated too. If you have had success with IVF/ICSI, please could you share any tips? What do you think made all the
MarshmellowMountain
in
Fertility Network UK
7 months ago
Is it just me !
So I had a viral infection in March and pneumonia that sent me into a really bad flare up of symptoms and I'm currently still in this flare up . Whenever I get any sort of infection it sends me into a flare of symptoms. I also had COVID in September which may be contributing to why my flare up is lasting
So I had a viral infection in March and pneumonia that sent me into a really bad flare up of symptoms and I'm currently still in this flare up . Whenever I get any sort of infection it sends me into a flare of symptoms. I also had COVID in September which may be contributing to why my flare up is lasting
Jillgib
in
Fibromyalgia Action UK
10 months ago
failed FET ☹️ next steps? More tests?
hi everyone, BFN today following a frozen transfer (it was a day 6, good quality embryo - not sure of the exact grading). I was told the embryo thawed perfectly and was hatching before transferred. My lining was 7.4 before I started the progesterone which I thought was borderline but the nurse used the
hi everyone, BFN today following a frozen transfer (it was a day 6, good quality embryo - not sure of the exact grading). I was told the embryo thawed perfectly and was hatching before transferred. My lining was 7.4 before I started the progesterone which I thought was borderline but the nurse used the
Prettypenny1
in
Fertility Network UK
7 months ago
8th COVID JAB REACTION??
I had my latest Covid vaccine 5 days ago; no reaction for the rest of that day (usual sore arm) but each day since I’ve become gradually more breathless upon exertion and thus light headed. My symptoms have worsened considerably ((couldn’t dress this morning without have to rest after each item was
I had my latest Covid vaccine 5 days ago; no reaction for the rest of that day (usual sore arm) but each day since I’ve become gradually more breathless upon exertion and thus light headed. My symptoms have worsened considerably ((couldn’t dress this morning without have to rest after each item was
CallMeSunny
in
NRAS
1 year ago
Am I getting back to hillwalking too soon?
Hello all, I've now been out of hospital for just over three months. I was admitted in February this year for flu, pneumonia and severe septic shock and was in a coma for almost a month in ICU, then in a general ward for another 8 weeks before getting out. I do have ICU-acquired weakness in various
Hello all, I've now been out of hospital for just over three months. I was admitted in February this year for flu, pneumonia and severe septic shock and was in a coma for almost a month in ICU, then in a general ward for another 8 weeks before getting out. I do have ICU-acquired weakness in various
helen_m
in
ICUsteps
1 year ago
Molnupiravir interactions with flecainide/tambocor
Hello everyone, On 9/24/23 i tested positive for covid for the first time. I discovered that Paxlovid is contraindicated for people taking flecainide. (I take 100mg, twice a day. ) My pharmacist noted that Molnupiravir (Lagevrio) was used as an alternative to Paxlovid for people in my situation. I
Hello everyone, On 9/24/23 i tested positive for covid for the first time. I discovered that Paxlovid is contraindicated for people taking flecainide. (I take 100mg, twice a day. ) My pharmacist noted that Molnupiravir (Lagevrio) was used as an alternative to Paxlovid for people in my situation. I
Wombat8
in
AF Association
1 year ago
Has prevnar13( pneumonia vaccine ) caused a trigger for people with existing inflammatory conditions?
I’m an autoimmune vasucliits patient . My inflammation in the eye was relatively managed well with immunosuppressants. But since having the Prevnar 13 , my inflammation is back in full swing . Has anyone experienced this ? If so, how have you resolved it ? Please advise .
I’m an autoimmune vasucliits patient . My inflammation in the eye was relatively managed well with immunosuppressants. But since having the Prevnar 13 , my inflammation is back in full swing . Has anyone experienced this ? If so, how have you resolved it ? Please advise .
Udupik
in
PMRGCAuk
10 months ago
Respite in South Bucks
HiI am new to this site. My lovely mum who is 78 lives with me after my healthy father passed away with covid in 2020. She was diagnosed with Parkinsons after a hip op severely damaged a nerve causing a drop foot. The neurologist just suggested she had it. So in 2019 I think she started these meds.
HiI am new to this site. My lovely mum who is 78 lives with me after my healthy father passed away with covid in 2020. She was diagnosed with Parkinsons after a hip op severely damaged a nerve causing a drop foot. The neurologist just suggested she had it. So in 2019 I think she started these meds.
MSACarer1000
in
Multiple System Atrophy Trust
1 year ago
Finally some progress
Those who followed our Journey, know this is such a painful process of grief. Two weeks ago, the hospital wrote it would not change the factual information in my wife's chart. In her chart it had been written she had Biopys proven Nash Cirrhosis, which led doctors looking at ultrasounds that said
Those who followed our Journey, know this is such a painful process of grief. Two weeks ago, the hospital wrote it would not change the factual information in my wife's chart. In her chart it had been written she had Biopys proven Nash Cirrhosis, which led doctors looking at ultrasounds that said
Wolivere
in
British Liver Trust
1 year ago
Heads Up
Got this text message yesterday. High risk in this context not related to age - OH is older than me and hasn’t had one. Wasn’t categorised as ‘high risk’ in last outbreak. I’ve looked into this and it seems that the ‘high risk’ criteria have been revised and that some neurological and psychiatric
Got this text message yesterday. High risk in this context not related to age - OH is older than me and hasn’t had one. Wasn’t categorised as ‘high risk’ in last outbreak. I’ve looked into this and it seems that the ‘high risk’ criteria have been revised and that some neurological and psychiatric
Hidden
in
Thyroid UK
1 year ago
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