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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
6 months ago
Glandular Fever virus and PMR?
Hello everyone, Does anyone know if the Glandular Fever virus could be linked with PMR? I contracted GF and Hepatitis B of the Liver in 2005, it took me 3 years to get over it and live my life normally, I took no drugs, it really was a case of rest and gentle exercise, the Drs warned me if I didn't
Hello everyone, Does anyone know if the Glandular Fever virus could be linked with PMR? I contracted GF and Hepatitis B of the Liver in 2005, it took me 3 years to get over it and live my life normally, I took no drugs, it really was a case of rest and gentle exercise, the Drs warned me if I didn't
MalloryMoss
in
PMRGCAuk
8 months ago
dienogest - shivers and cold
Hi everyone. Am on day 3 of taking dienogest and since yesterday I have been feeling freezing cold and shivery, also getting numb hands, and the veins on my arms and legs very visible (like a circulatory problem). Otherwise feel ok. Anyone else had this as a side effect? Wondering if it is related or
Hi everyone. Am on day 3 of taking dienogest and since yesterday I have been feeling freezing cold and shivery, also getting numb hands, and the veins on my arms and legs very visible (like a circulatory problem). Otherwise feel ok. Anyone else had this as a side effect? Wondering if it is related or
TandE
in
Endometriosis UK
2 months ago
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Sensitive. Stopping Crinone Qn
hi everyone. Please don’t read if you’re not in the right headspace. I’ve very luckily had a BFP on my second fresh icsi cycle with NhS. I’m currently 15dp3dt of two embryos and have been told that I don’t need to use the Crinone gel anymore. I’ve a few more left from my previous private cycle and
hi everyone. Please don’t read if you’re not in the right headspace. I’ve very luckily had a BFP on my second fresh icsi cycle with NhS. I’m currently 15dp3dt of two embryos and have been told that I don’t need to use the Crinone gel anymore. I’ve a few more left from my previous private cycle and
Clayhugs
in
Fertility Network UK
7 months ago
Taking Flecainide with Bisoprolol
When I was first diagnosed with AF a few years ago I was told to use the "pill in the pocket" approach to terminate an episode by using bisoprolol and flecainide - the flecainide 20 minutes after the bisoprolol. Now, for the last year I've been on bisoprolol 1.25mg daily and just take the occasional
When I was first diagnosed with AF a few years ago I was told to use the "pill in the pocket" approach to terminate an episode by using bisoprolol and flecainide - the flecainide 20 minutes after the bisoprolol. Now, for the last year I've been on bisoprolol 1.25mg daily and just take the occasional
Barny12
in
AF Association
1 year ago
mouth ulcer
i’ve only just got over my constipation problem and now a problem that’s so painful. my lip started throbbing two days ago them i woke up and it has gone so big. then a blister/ cold sore i don’t know which appeared. the throbbing and burning pain is constantly here. earlier i’ve noticed pain on my tounge
i’ve only just got over my constipation problem and now a problem that’s so painful. my lip started throbbing two days ago them i woke up and it has gone so big. then a blister/ cold sore i don’t know which appeared. the throbbing and burning pain is constantly here. earlier i’ve noticed pain on my tounge
Junny123
in
Pain Concern
2 months ago
the never ending hurdles
When we did our 2nd icsi cycle we were told there was a 2% chance of total fertilisation failure, well, we were the 2% and none of our eggs fertilised. Now when pgta testing following our 3rd cycle we were told there was a 2% chance our embryos wouldn’t survive the thaw…and guess what, our top graded
When we did our 2nd icsi cycle we were told there was a 2% chance of total fertilisation failure, well, we were the 2% and none of our eggs fertilised. Now when pgta testing following our 3rd cycle we were told there was a 2% chance our embryos wouldn’t survive the thaw…and guess what, our top graded
Hidden
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
10 months ago
Pneumonia Vaccine
I was talking to a very friendly Doctors wife yesterday who works on his admin and we talked about the amount of people suffering and in some cases hospitalised with pneumonia. She said that the vaccine I was given about 10yrs ago is now not considered to be sufficient protection. It is thought that
I was talking to a very friendly Doctors wife yesterday who works on his admin and we talked about the amount of people suffering and in some cases hospitalised with pneumonia. She said that the vaccine I was given about 10yrs ago is now not considered to be sufficient protection. It is thought that
Ridge
in
PMRGCAuk
6 months ago
Shingles
I have CFS/ME, Fibromyalgia etcMy previous doctor from when I moved new what I had etc. I have had shingles maybe three times. But I can't understand why they have message my husband, who is younger then me and as diabetes for the first time for a shingles injections and he as never had shingles? Any
I have CFS/ME, Fibromyalgia etcMy previous doctor from when I moved new what I had etc. I have had shingles maybe three times. But I can't understand why they have message my husband, who is younger then me and as diabetes for the first time for a shingles injections and he as never had shingles? Any
sharron1
in
Fibromyalgia Action UK
8 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
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
10 months ago
adrenals
please help , I am feeling really unwell ,dizzy , feel sick ,mentally very low,upset stomach,lost weight ,waking up after 4 hours sleep ,anxiety of the scale.from July till October tapered down from 6mg to 4.5 finished 28 October,stayed there to see how I was , I wasn’t feeling brilliant but I know I
please help , I am feeling really unwell ,dizzy , feel sick ,mentally very low,upset stomach,lost weight ,waking up after 4 hours sleep ,anxiety of the scale.from July till October tapered down from 6mg to 4.5 finished 28 October,stayed there to see how I was , I wasn’t feeling brilliant but I know I
Amilee
in
PMRGCAuk
8 months ago
Chillblains
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
I have SLL and recently have had a few occurrences of Chillblains, my son is a Consultant Haematologist and tells me haematological malignancy is a common link and this paper links it to SLL, https://bmcdermatol.biomedcentral.com/articles/10.1186/s12895-015-0032-z. I can cope with this keeping hands
GerryPL
in
CLL Support
8 months ago
asthma cough
I’d love it if anyone has any tips for calming an asthma cough without resorting to steroid tablets. It’s only just over a month since my last lot and I’d really like to try and avoid them if possible. It’s driving me and everyone else mad!
I’d love it if anyone has any tips for calming an asthma cough without resorting to steroid tablets. It’s only just over a month since my last lot and I’d really like to try and avoid them if possible. It’s driving me and everyone else mad!
Gymbearo
in
Asthma Community Forum
2 months ago
raised euthyrox and i get cough morning night to the point of choking and is strips of pink blood
every morning i get rib throat and cough with strips of pink blood . also wher thyroid is located is sore to swalow and night time i cough same thing all day after the morning i dont cough i just sore when i swallow i dont have cold it feel as if my thyroid swolen up and is making me
every morning i get rib throat and cough with strips of pink blood . also wher thyroid is located is sore to swalow and night time i cough same thing all day after the morning i dont cough i just sore when i swallow i dont have cold it feel as if my thyroid swolen up and is making me
morcan54
in
Thyroid UK
2 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
10 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
10 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
10 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
10 months ago
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