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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
9 months ago
Hepatic Peliosis (What is it?)
RE: Hepatic Peliosis (What is it?) Hi all, I have been diagnosed with Hepatic Peliosis of the liver. What is it? and is there any treatments please? Does anyone else have Hepatic Peliosis ? How are your dealing with this etc? Any information would be helpful. Thank you. Regards, Kevin Walker
RE: Hepatic Peliosis (What is it?) Hi all, I have been diagnosed with Hepatic Peliosis of the liver. What is it? and is there any treatments please? Does anyone else have Hepatic Peliosis ? How are your dealing with this etc? Any information would be helpful. Thank you. Regards, Kevin Walker
kevpwalker
in
British Liver Trust
4 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
9 months ago
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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
9 months 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
9 months 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
9 months 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
9 months 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
9 months ago
Dizzy
Good morning to you all.I've been diagnosed with fibomyaigia in 2020 But I am getting real dizzy it's lasted for a couple of weeks now at first I got up at night and couldn't walk at all in a straight line everything was spinning so scary. The doctor said I have Benign paroxysmal positional vertigo
Good morning to you all.I've been diagnosed with fibomyaigia in 2020 But I am getting real dizzy it's lasted for a couple of weeks now at first I got up at night and couldn't walk at all in a straight line everything was spinning so scary. The doctor said I have Benign paroxysmal positional vertigo
Chellelo
in
Fibromyalgia Action UK
8 months ago
Has anyone had more fertilised eggs 2nd time round with ICSI?
Hi everyone, I'm wondering if anyone undergoing ICSI had a more successful round of fertilised eggs 2nd time round and if there was anything you done differently? We had our first round in August and they managed to use 10 mature eggs after collecting 15 eggs, 24 hours later we were told that only
Hi everyone, I'm wondering if anyone undergoing ICSI had a more successful round of fertilised eggs 2nd time round and if there was anything you done differently? We had our first round in August and they managed to use 10 mature eggs after collecting 15 eggs, 24 hours later we were told that only
WMolly88
in
Fertility Network UK
6 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
9 months 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
9 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
9 months 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
9 months ago
Covid and steroid increase
I’m sure this has been answered before so apologies. I have Covid and on 2.75mg of steroids. Should I increase for few days or should I see how it goes? Thanks
I’m sure this has been answered before so apologies. I have Covid and on 2.75mg of steroids. Should I increase for few days or should I see how it goes? Thanks
Rosina1871
in
PMRGCAuk
9 months ago
IVIG - how soon does it benefit?
My husband - CLL, on Calquence since April 2021 - has begun a schedule of monthly IVIG, mainly because he had 2 life threatening infections late spring/early summer (staph that went rogue, followed by c. Diff thanks to months of antibiotics). His ID doc has said that the IG may likely have Covid antibodies
My husband - CLL, on Calquence since April 2021 - has begun a schedule of monthly IVIG, mainly because he had 2 life threatening infections late spring/early summer (staph that went rogue, followed by c. Diff thanks to months of antibiotics). His ID doc has said that the IG may likely have Covid antibodies
OaktownA
in
CLL Support
9 months ago
Herpes (or acyclovir usage) affecting implantation after ivf embryo transfer?
I have had herpes for about 10 years. I have noticed more outbreaks during stims. I've already had 2 failed transfers and am worried both that having herpes and /or taking acyclovir will affect implantation for my last transfer. I've read some conflicting studies on acyclovir and it's effect on implantation
I have had herpes for about 10 years. I have noticed more outbreaks during stims. I've already had 2 failed transfers and am worried both that having herpes and /or taking acyclovir will affect implantation for my last transfer. I've read some conflicting studies on acyclovir and it's effect on implantation
Norregirl
in
Fertility Network UK
4 months ago
Haven't ran in over 18 months
Due to pantar fasciitis I haven't ran for over 18 months. Earlier this year I tried shockwave therapy which eased the pain by about 15% Almost two weeks ago I managed to get a steroid injection. The doctor who performed the injection said it should take about two weeks to see any difference. Well after
Due to pantar fasciitis I haven't ran for over 18 months. Earlier this year I tried shockwave therapy which eased the pain by about 15% Almost two weeks ago I managed to get a steroid injection. The doctor who performed the injection said it should take about two weeks to see any difference. Well after
Shaunie75
in
Couch to 5K
9 months ago
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
9 months ago
Dr. "Snuffy" Myers daughter talks about the day she heard about her Dad's diagnosis
https://youtu.be/k0vmB-fgxQc Click here to subscribe: https://www.youtube.com/c/malecare?sub_confirmation=1 Jessie Myers, daughter of prostate cancer legend Dr. "Snuffy" Myers, talks about the day she heard about her Dad's diagnosis and how she and her family came to terms with death and prostate
https://youtu.be/k0vmB-fgxQc Click here to subscribe: https://www.youtube.com/c/malecare?sub_confirmation=1 Jessie Myers, daughter of prostate cancer legend Dr. "Snuffy" Myers, talks about the day she heard about her Dad's diagnosis and how she and her family came to terms with death and prostate
Darryl
Partner
in
Advanced Prostate Cancer
4 months ago
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