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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
11 months ago
Flu won’t go away.
I was diagnosed four years ago with emphysema. I have had no symptoms. Six weeks ago I got the flu. It’s been a rough six weeks. Getting my breath back and my energy back. Now every morning I can’t breathe and have to use an inhaler. Never had to before. I’ve had a CAT scan of my lungs, and it has not
I was diagnosed four years ago with emphysema. I have had no symptoms. Six weeks ago I got the flu. It’s been a rough six weeks. Getting my breath back and my energy back. Now every morning I can’t breathe and have to use an inhaler. Never had to before. I’ve had a CAT scan of my lungs, and it has not
Rkdevo
in
Lung Conditions Community Forum
5 months ago
Another day another other saga!!You couldn’t make it up!
Thanks everyone for your advice yesterday. It’s been a learning curve & I will be able to navigate better next time. I went to A & E first thing & in triage the nurse said it’s sounds like you have flu. So she did a nasal swab. She asked me to wear a mask & I said oh I’ve done a Covid test. She said
Thanks everyone for your advice yesterday. It’s been a learning curve & I will be able to navigate better next time. I went to A & E first thing & in triage the nurse said it’s sounds like you have flu. So she did a nasal swab. She asked me to wear a mask & I said oh I’ve done a Covid test. She said
Otto11
in
Lung Conditions Community Forum
5 months ago
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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
11 months ago
Diagnosis
This is my 4th week in hospital. I’ve had 3 chest x-rays, ct scans and mris of all the bony bits of my body to try and find the source of infection that was showing with spikes in temperature, they told me I’ve got pneumonia!
This is my 4th week in hospital. I’ve had 3 chest x-rays, ct scans and mris of all the bony bits of my body to try and find the source of infection that was showing with spikes in temperature, they told me I’ve got pneumonia!
helenlw7
in
Lung Conditions Community Forum
5 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
11 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
11 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
11 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
11 months ago
Questions about experience with rinvoq
Have had to stop rinvoq a few times lately due to infections, this last time I stopped rinvoq for ear infection for 5 days. The infection has not cleared up so they're giving me another antibiotic for 10 days. I was just wondering if most people have a flare when stopping rinvoq for that length of
Have had to stop rinvoq a few times lately due to infections, this last time I stopped rinvoq for ear infection for 5 days. The infection has not cleared up so they're giving me another antibiotic for 10 days. I was just wondering if most people have a flare when stopping rinvoq for that length of
gnstric66
in
NRAS
10 months ago
mini pill to stop ovulation/ interstitial cystitis or Endo?
Hi all i am on the waiting list for Laparoscopy as I have all the symptoms, plus I have confirmed PCOS from scans- I am 44 so can’t take the combined pill but my mid cycle is horrendous! Bladder pain, rectal pain and bleeding, leg pain and severe pelvic pain more so on left hand side, painful sex, nausea
Hi all i am on the waiting list for Laparoscopy as I have all the symptoms, plus I have confirmed PCOS from scans- I am 44 so can’t take the combined pill but my mid cycle is horrendous! Bladder pain, rectal pain and bleeding, leg pain and severe pelvic pain more so on left hand side, painful sex, nausea
SJ0514
in
Endometriosis UK
1 year ago
Covid Antivirals
Hi, if we get Covid is it still advisable for us to ask for the antivirals or is it so mild now that patients with blood cancers don’t need them? Suzy
Hi, if we get Covid is it still advisable for us to ask for the antivirals or is it so mild now that patients with blood cancers don’t need them? Suzy
SDJD
in
MPN Voice
11 months ago
egg collection and bad cold/flu
Once again I’m a cheap date and after only one week of stims I’ve triggered last night for egg collection tomorrow morning (Thursday) everything looks about the same as last few times about 7-8 follicles ready (between 17-22mm) and some others not far behind. I am really worried though as I had a bit
Once again I’m a cheap date and after only one week of stims I’ve triggered last night for egg collection tomorrow morning (Thursday) everything looks about the same as last few times about 7-8 follicles ready (between 17-22mm) and some others not far behind. I am really worried though as I had a bit
Twiglet2
in
Fertility Network UK
5 months ago
Covid infection initiating PMR flareup
I have tested positive for Covid.. it has initiated a PMR flare-up. Gp suggested increasing prednisolone for 3 or 4 days to 13mg, I had reduced to 9mg. Then reduce 1mg / day to 9. Anyone else had a flare up related to covid (I have ha d 6 vaccination re covid) 0
I have tested positive for Covid.. it has initiated a PMR flare-up. Gp suggested increasing prednisolone for 3 or 4 days to 13mg, I had reduced to 9mg. Then reduce 1mg / day to 9. Anyone else had a flare up related to covid (I have ha d 6 vaccination re covid) 0
attempttocycycle
in
PMRGCAuk
11 months ago
COVID vaccine
Writing on behalf of a friend, to see if anyone has had similar. Her husband (in his 80sdoesnt) is due to get his vaccines . He has RA. Every time he gets the COVID vaccine he is terrible for 25-36 hours afterwards. Totally disorientated, confused, doesn't know where he is etc etc. She doesn't know what
Writing on behalf of a friend, to see if anyone has had similar. Her husband (in his 80sdoesnt) is due to get his vaccines . He has RA. Every time he gets the COVID vaccine he is terrible for 25-36 hours afterwards. Totally disorientated, confused, doesn't know where he is etc etc. She doesn't know what
Hodc
in
NRAS
11 months ago
I'd just like to know
Hi, I had a terrible cough over Christmas, gradually got better over the next two weeks but still had some rib pain mid Jan so saw my GP. I'd stopped smoking because of the cough but had smoked most of my adult life. (still stopped, will never again) I had no cancer symptoms except the rib pain but
Hi, I had a terrible cough over Christmas, gradually got better over the next two weeks but still had some rib pain mid Jan so saw my GP. I'd stopped smoking because of the cough but had smoked most of my adult life. (still stopped, will never again) I had no cancer symptoms except the rib pain but
Chips4tea
in
The Roy Castle Lung Cancer Foundation
5 months ago
The forgotten half million?
We went from Shielding to being High Risk to being Vulnerable. Are we now the Forgotten? I ask, because we were told that the Autumn vaccination programme was starting on 18th September, and I started to hear of people getting appointments and inoculations but from my knowledge of their condition and
We went from Shielding to being High Risk to being Vulnerable. Are we now the Forgotten? I ask, because we were told that the Autumn vaccination programme was starting on 18th September, and I started to hear of people getting appointments and inoculations but from my knowledge of their condition and
quanglewangle
in
MPN Voice
11 months ago
Latest Study Re Long Covid
Given the recent posts about the the next Covid vaccination boosters, I thought people might find thi interesting. BBC News - Long Covid: MRI scans reveal new clues to symptoms https://www.bbc.co.uk/news/health-66890505
Given the recent posts about the the next Covid vaccination boosters, I thought people might find thi interesting. BBC News - Long Covid: MRI scans reveal new clues to symptoms https://www.bbc.co.uk/news/health-66890505
Bcol
in
PMRGCAuk
11 months ago
Pneumonia
HiJust wondering how long people have taken to recover from pneumonia. . Was in hospital for 6 days. Although I know I am on the mend I was wondering what other peoples experience were. I have asthma and bronchietasis. I am feeling very sorry for myself.. Appreciate any reply. Xx
HiJust wondering how long people have taken to recover from pneumonia. . Was in hospital for 6 days. Although I know I am on the mend I was wondering what other peoples experience were. I have asthma and bronchietasis. I am feeling very sorry for myself.. Appreciate any reply. Xx
teddyd
in
Lung Conditions Community Forum
10 months ago
iui or ivf?
if ovulation induction hasn’t been successful (I ovulate, but have breakthrough bleeding) what do you think they may suggest next? Any previous experiences? Xxx
if ovulation induction hasn’t been successful (I ovulate, but have breakthrough bleeding) what do you think they may suggest next? Any previous experiences? Xxx
Disneywife
in
Fertility Network UK
10 months ago
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