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Hi all an update on my new rheumy
Hi everybody, yesterday evening I had an appointment with my new Rheumy. I was actually dreading it due to my last experience with the previous rheumatologist. Well I have to say he was brilliant listened to me, Then going on my symptoms and doing an ultrasound on my hands and looking at all my blood
Hi everybody, yesterday evening I had an appointment with my new Rheumy. I was actually dreading it due to my last experience with the previous rheumatologist. Well I have to say he was brilliant listened to me, Then going on my symptoms and doing an ultrasound on my hands and looking at all my blood
Wonderfullifeandmore
in
PMRGCAuk
1 year ago
PGT-A testing
Hi everyone, just planning my 3rd cycle and have the option of PGT-A testing...I had 2 cycles, 3 transfers and 1 pregnancy which ended with MMC 2 years ago... 😪 I just turned to 40 the dreadded number... I am new to PGT-A testing... Anybody could give me some pros and cons with it and if you recommend
Hi everyone, just planning my 3rd cycle and have the option of PGT-A testing...I had 2 cycles, 3 transfers and 1 pregnancy which ended with MMC 2 years ago... 😪 I just turned to 40 the dreadded number... I am new to PGT-A testing... Anybody could give me some pros and cons with it and if you recommend
MagicTourmaline
in
Fertility Network UK
8 months ago
Gamma light and Alzheimers - free app
I know this is not specific to PD, but thought I'd share this article. You all have been so kind to share new advancements, thank you. This looks very interesting!!! https://www.cogentica.com/alzheimers-research-gamma/ Direct from the article: (also talks about bacteria and gamma light and sound
I know this is not specific to PD, but thought I'd share this article. You all have been so kind to share new advancements, thank you. This looks very interesting!!! https://www.cogentica.com/alzheimers-research-gamma/ Direct from the article: (also talks about bacteria and gamma light and sound
Kat343
in
Cure Parkinson's
11 months ago
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RLS and Covid vaccine
Just for everyones awareness, my RLS was way worsened by the covid vaccine and so far it seems to have been a permanent side effect. I had RLS since I was a kid but tyically lasted 10 to 30 minutes each night whereas after the vaccine (within days) it shot up to 2 to 3 hours. I wanted to make sure I
Just for everyones awareness, my RLS was way worsened by the covid vaccine and so far it seems to have been a permanent side effect. I had RLS since I was a kid but tyically lasted 10 to 30 minutes each night whereas after the vaccine (within days) it shot up to 2 to 3 hours. I wanted to make sure I
the7thsong
in
Restless Legs Syndrome
1 year ago
Rejected for anti virals
Hi everyone I tested positive for Covid on Tuesday and reported it to my GP surgery on Wednesday. I heard from Chelsea and Westminster Hospital on Thursday. They asked about how active my Lupus had been and I told them recently it had been pretty well controlled and they asked how it affected me and
Hi everyone I tested positive for Covid on Tuesday and reported it to my GP surgery on Wednesday. I heard from Chelsea and Westminster Hospital on Thursday. They asked about how active my Lupus had been and I told them recently it had been pretty well controlled and they asked how it affected me and
BookishVibes
in
LUPUS UK
1 year ago
Flying with liquid medication
I go on holiday in a couple of weeks and need to take all my needles and lubion as well as Tinzaparin. Although they are less than 100ml in each vial/syringe, collectively they’ll be more than 100ml. Do I just need to take my prescription or do I have to declare the meds or get in touch with the airports
I go on holiday in a couple of weeks and need to take all my needles and lubion as well as Tinzaparin. Although they are less than 100ml in each vial/syringe, collectively they’ll be more than 100ml. Do I just need to take my prescription or do I have to declare the meds or get in touch with the airports
Alwaysbelieving
in
Fertility Network UK
11 months ago
Urgency and necessity of Epstein-Barr virus prophylactic vaccines
In the light of many previous posts mentioning Epstein-Barr virus (EBV), I think this new paper is likely of interest and relevance. However, vaccine discussions have proved to be contentious and, with none of us being vaccine or virus experts, I have decided to close this post to replies. [i]
Urgency
In the light of many previous posts mentioning Epstein-Barr virus (EBV), I think this new paper is likely of interest and relevance. However, vaccine discussions have proved to be contentious and, with none of us being vaccine or virus experts, I have decided to close this post to replies. [i]
Urgency
helvella
Thyroid UK
in
Thyroid UK
2 years ago
Paxlovid for Covid if you have PMR
hi all. Living in France for 5 months didn’t think I would get Covid here but I did. I think it came with our guests on the plane. But in any case I have Paxlovid with me but I keep seeing things that say don’t take it if you have autoimmune disorder. Is that us? My doctor gave it to me but…. I am down
hi all. Living in France for 5 months didn’t think I would get Covid here but I did. I think it came with our guests on the plane. But in any case I have Paxlovid with me but I keep seeing things that say don’t take it if you have autoimmune disorder. Is that us? My doctor gave it to me but…. I am down
bluegirl7
in
PMRGCAuk
1 year ago
post op pneumonia
my step daughter in law had op for removal of cancerous growth from lung 3 weeks ago . and now has pneeumonia 70 odd . should they have been warned about that ? and I didnt think either . i do hope she hasnt got a resistant hospital strain .
my step daughter in law had op for removal of cancerous growth from lung 3 weeks ago . and now has pneeumonia 70 odd . should they have been warned about that ? and I didnt think either . i do hope she hasnt got a resistant hospital strain .
Jaybird19
in
Lung Conditions Community Forum
10 months ago
Dreading seeing the Rheumatologist
Hi everyone, I have an appointment coming up with my Rheumatologist which I’ve been under for the last 3 1/2 years (I’m in the UK, we don’t get a choice in who we see). It took him a couple of years to finally diagnose PMR. During that time I’d become almost housebound. He insisted I take the
Hi everyone, I have an appointment coming up with my Rheumatologist which I’ve been under for the last 3 1/2 years (I’m in the UK, we don’t get a choice in who we see). It took him a couple of years to finally diagnose PMR. During that time I’d become almost housebound. He insisted I take the
Bramble2000
in
PMRGCAuk
1 year ago
Sensitive : BFP rainbow baby
I was in two minds if to write this post as I know how difficult it is to read these updates if you are still struggling. and the fact that I am still in shock at a positive result. But I would also like to share a story of hope. So some of you will know my history, we had success on our second ICSI
I was in two minds if to write this post as I know how difficult it is to read these updates if you are still struggling. and the fact that I am still in shock at a positive result. But I would also like to share a story of hope. So some of you will know my history, we had success on our second ICSI
butterfliez
in
Fertility Network UK
7 months ago
Hand foot and mouth before transfer
My LB has been diagnosed with hand foot and mouth today and I've now started with a sore throat and thinking the worst. I've had EC today and all going well should be having a tenasfer on 14 December. If I do get the spots I assume my transfer will need to be cancelled and they'd do a freeze all. Is
My LB has been diagnosed with hand foot and mouth today and I've now started with a sore throat and thinking the worst. I've had EC today and all going well should be having a tenasfer on 14 December. If I do get the spots I assume my transfer will need to be cancelled and they'd do a freeze all. Is
Sw1234
in
Fertility Network UK
2 years ago
Methylene Blue
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Has anyone used or considered Methylene Blue in very low dosages for their Parkinson's? Franciso Gonzalez-Lima of the University of Texas, Austin is an expert on its advantages for treating neurological diseases. Mercola did an interview with him on the subject. Mercola does not promote synthetic drugs
Trailing
in
Cure Parkinson's
1 year ago
Flare and due COVID jab Friday
Hi all. I hope you are all well or as well as can be. 🙂 I'm booked for my spring COVID booster tomorrow but I'm starting to flare, sore hands and shoulders etc and they are starting me on hydroxychloroquine next week as well as the 3g if sulfasalazine I'm already on. Have any of you had the jab whilst
Hi all. I hope you are all well or as well as can be. 🙂 I'm booked for my spring COVID booster tomorrow but I'm starting to flare, sore hands and shoulders etc and they are starting me on hydroxychloroquine next week as well as the 3g if sulfasalazine I'm already on. Have any of you had the jab whilst
Haz58
in
NRAS
1 year ago
stress/upset at waiting times
Hi All, We are still waiting to start our treatment after being referred for ICSI in August this year. We had a further consult today and have decided to go down the donor route due to male factor infertility ( severely low count ). We have been told that we could be looking up to a 12 month wait and
Hi All, We are still waiting to start our treatment after being referred for ICSI in August this year. We had a further consult today and have decided to go down the donor route due to male factor infertility ( severely low count ). We have been told that we could be looking up to a 12 month wait and
Summeringreece
in
Fertility Network UK
7 months ago
Long awaited/ Neglected review
Hello,, My name is Cat, I had a heart attack in 2018. I was put on the Gold standard medications, after having two stents fitted to my LAD. I had my cardiac rehabilitation and later reviewed . I was given the all clear. I started working full time again and then covid hit. Everything was okay until
Hello,, My name is Cat, I had a heart attack in 2018. I was put on the Gold standard medications, after having two stents fitted to my LAD. I had my cardiac rehabilitation and later reviewed . I was given the all clear. I started working full time again and then covid hit. Everything was okay until
Katydl
in
British Heart Foundation
1 year ago
Follow up from my post about cellulitis
Sorry should have said that I am on 10 mg of Pred.
Sorry should have said that I am on 10 mg of Pred.
Dobermanlover
in
PMRGCAuk
11 months ago
CELLULITIS
Has anyone had cellulitis? I have had it for just over a week and have just completed a 7 day course of Flucloxacillin. I did not see a doctor - just had to post a photo of my leg, so haven't had the opportunity of discussing it with him. From the web it sounds quite serious, but don't like taking
Has anyone had cellulitis? I have had it for just over a week and have just completed a 7 day course of Flucloxacillin. I did not see a doctor - just had to post a photo of my leg, so haven't had the opportunity of discussing it with him. From the web it sounds quite serious, but don't like taking
Dobermanlover
in
PMRGCAuk
11 months ago
Slow, slow, quick quick slow -to taper or not?
I've forgotten the name of the tapering method. It's come to me in an hour or so I am sure. Canada was amazing and exhausting, we've been back since the 31st May and are still recovering. Mark was diagnosed with OA in his knees in March. Despite steroid injections before we left, his knees did not
I've forgotten the name of the tapering method. It's come to me in an hour or so I am sure. Canada was amazing and exhausting, we've been back since the 31st May and are still recovering. Mark was diagnosed with OA in his knees in March. Despite steroid injections before we left, his knees did not
IdasMum
in
PMRGCAuk
1 year ago
osteoarthritis hip pain
I have so much pain in my hip when walking I have asked to be referred for further help from my doctor. I have had steroid injection x 2 without success and continue to take Cocodamol 8/500 as prescribed now b’cos of pain have been prescribed codeine phosphate 15mg, any advice Would be welcome
I have so much pain in my hip when walking I have asked to be referred for further help from my doctor. I have had steroid injection x 2 without success and continue to take Cocodamol 8/500 as prescribed now b’cos of pain have been prescribed codeine phosphate 15mg, any advice Would be welcome
Margie21
in
Osteoarthritis Action
1 year ago
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