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Adrenal cortex extract (ACE)
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Recurrent vaginal thrush- need urgent help
I had what looks like a vaginal thrush for the first time 3 weeks back. I'm 35 yrs old. My GP nurse saw me and suggested Canesten pessary. I took it but to no avail (also the pessary did not work properly) I went back to the doctor in 2 days and she suggested Flucanazole oral tabled (150 mg 1 dose) that
I had what looks like a vaginal thrush for the first time 3 weeks back. I'm 35 yrs old. My GP nurse saw me and suggested Canesten pessary. I took it but to no avail (also the pessary did not work properly) I went back to the doctor in 2 days and she suggested Flucanazole oral tabled (150 mg 1 dose) that
Rita89
in
Women's Health
5 months ago
Aciclovir as prevention for shingles
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
RamsesII
in
CLL Support
5 months ago
Bad reaction to progynova
hi, has one experienced a bad reaction to taking progynova? I’ve got a large red raw hand rash and swollen eyes because of this had to cancel my planned fet😩 seems like I have an allergy
hi, has one experienced a bad reaction to taking progynova? I’ve got a large red raw hand rash and swollen eyes because of this had to cancel my planned fet😩 seems like I have an allergy
keepfaith1982
in
Fertility Network UK
5 months ago
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Dialysis / RLS
Wow, this sub is a lot more active than the Kidney Disease sub, one would think it would be the other way around. I guess RLS is a lot more prevalent than people think? I never experienced or even heard of RLS before starting dialysis but boy did it hit me hard. It's already hard to sleep while doing
Wow, this sub is a lot more active than the Kidney Disease sub, one would think it would be the other way around. I guess RLS is a lot more prevalent than people think? I never experienced or even heard of RLS before starting dialysis but boy did it hit me hard. It's already hard to sleep while doing
bumblebee_tuna
in
Restless Legs Syndrome
11 months ago
ACTH Cortisol test enquiry
Afternoon all I had an ACTH test done at the request of my GP because my early morning blood cortisol test was 133 (ref 113 - 532). I am attaching 2 pages of results. The consultant says I'm fine but I want to run it past folk on here because I'm not so sure. I certainly don't feel fine. I don't understand
Afternoon all I had an ACTH test done at the request of my GP because my early morning blood cortisol test was 133 (ref 113 - 532). I am attaching 2 pages of results. The consultant says I'm fine but I want to run it past folk on here because I'm not so sure. I certainly don't feel fine. I don't understand
smilingjane
in
Thyroid UK
1 year 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
5 months ago
Stage 5 Chronic Kidney Disease (CKD)
Dialysis and kidney transplant are the only two treatments for people with kidney failure. It is also important for patients to continue managing any other health conditions they may have, including high blood pressure and/or diabetes. Learn more at: https://www.kidney.org/atoz/content/stage-5-chronic-kidney-disease-ckd
Dialysis and kidney transplant are the only two treatments for people with kidney failure. It is also important for patients to continue managing any other health conditions they may have, including high blood pressure and/or diabetes. Learn more at: https://www.kidney.org/atoz/content/stage-5-chronic-kidney-disease-ckd
JackieJ_NKF
Partner
in
Kidney Dialysis
11 months ago
considering stopping adt/abiraterone to see what happens
it’s been 8 months since I found myself to have a PSA of 70, it is now 0.0 and I am due for the ADT injection. I have coupled standard treatment with rife, mushrooms, ivermectin, fenbendazole, apricot seeds, green tea, vit e, graviola. What is the feeling on the board here should I see if the alternative
it’s been 8 months since I found myself to have a PSA of 70, it is now 0.0 and I am due for the ADT injection. I have coupled standard treatment with rife, mushrooms, ivermectin, fenbendazole, apricot seeds, green tea, vit e, graviola. What is the feeling on the board here should I see if the alternative
Nowhereman9
in
Advanced Prostate Cancer
5 months ago
Lanzoprazole and low B12
Hi guys I am worried and I don’t know if I am worried about nothing. In a nutshell, in 2018 hubby starts heart meds and has done so ever since. One of which is landoprazole 15mg every day. Purpose to protect his stomach from the potential harm from taking 75mg asprin to thin his blood. A couple
Hi guys I am worried and I don’t know if I am worried about nothing. In a nutshell, in 2018 hubby starts heart meds and has done so ever since. One of which is landoprazole 15mg every day. Purpose to protect his stomach from the potential harm from taking 75mg asprin to thin his blood. A couple
Wwwdot
in
Pernicious Anaemia Society
1 year ago
Seeking information about encephalomalacia
Hi , I’m new to this site . I have recently given up working to become a carer for my partner who had a TBI in 2009 . He received a bleed to the brain and had to have a craniotomy . Amazingly he recovered and even went back to work but in 2018 I noticed a change in his walking and a movement in his eye
Hi , I’m new to this site . I have recently given up working to become a carer for my partner who had a TBI in 2009 . He received a bleed to the brain and had to have a craniotomy . Amazingly he recovered and even went back to work but in 2018 I noticed a change in his walking and a movement in his eye
Jasper65
in
Headway
5 months ago
New to PMR
Hi, just joined up. I'm coming up 48 and my GP has recently diagnosed me with PMR. I've had pains now since May 2021 so been 2 years of pains, scans, bloods, ultrasounds, pregabelin. The ultrasounds showed up I have calcification and bursitis in both my hips (trocherantic) and both shoulders. I've been
Hi, just joined up. I'm coming up 48 and my GP has recently diagnosed me with PMR. I've had pains now since May 2021 so been 2 years of pains, scans, bloods, ultrasounds, pregabelin. The ultrasounds showed up I have calcification and bursitis in both my hips (trocherantic) and both shoulders. I've been
Monkey321
in
PMRGCAuk
1 year ago
What causes cold sweats?
I’ve been taking Prednisolone for PMR since May 2021. I’ve been very gradually reducing and have been on 4mg for 1 month. I take the Pred at about 5am with yoghourt and banana. I had Covid 2 weeks ago. I didn’t up the Pred dose. I have no PMR pain. I feel ok in the mornings but have high anxiety
I’ve been taking Prednisolone for PMR since May 2021. I’ve been very gradually reducing and have been on 4mg for 1 month. I take the Pred at about 5am with yoghourt and banana. I had Covid 2 weeks ago. I didn’t up the Pred dose. I have no PMR pain. I feel ok in the mornings but have high anxiety
Geology
in
PMRGCAuk
16 hours ago
Feeling cold all the time
Hi, I have scleroderma and reynauds and while I am used to having cold hands and feet of late I am very cold all over, even my core. I was wondering if I might be low on some vitamins or minerals and was hoping someone might be able to advise. Regards, Darren
Hi, I have scleroderma and reynauds and while I am used to having cold hands and feet of late I am very cold all over, even my core. I was wondering if I might be low on some vitamins or minerals and was hoping someone might be able to advise. Regards, Darren
Deiseboy
in
Scleroderma & Raynaud's UK (SRUK)
2 days ago
PV and common Cold
Morning all, Only diagnosed with PV since Nov 23. Low risk as im 38 and platelets have stopped increasing since the introduction of aspirin and a few other for the itch. In the last 2 months it feels like im constantly battling a cold. I get slight relief for a few days and then its back. Anyone else
Morning all, Only diagnosed with PV since Nov 23. Low risk as im 38 and platelets have stopped increasing since the introduction of aspirin and a few other for the itch. In the last 2 months it feels like im constantly battling a cold. I get slight relief for a few days and then its back. Anyone else
Headaball
in
MPN Voice
3 days ago
Is pseudamonas contagious??
Hi, Does anyone know if my pseudamonas could be transmitted to those who live in close proximity? I always thought not but I've been worried about my OH's persistent cough - I know there could be many other reasons for his cough and his recent sputum test was clear but....
Hi, Does anyone know if my pseudamonas could be transmitted to those who live in close proximity? I always thought not but I've been worried about my OH's persistent cough - I know there could be many other reasons for his cough and his recent sputum test was clear but....
Leafsweeper
in
Lung Conditions Community Forum
5 days ago
freezyfeet
Nothing seems to help with cold feet except my heated mat and gloves for my hands.
Nothing seems to help with cold feet except my heated mat and gloves for my hands.
Freezyfeet
in
Scleroderma & Raynaud's UK (SRUK)
6 days ago
UK winter flu vaccines, booking available
Boots are now taking bookings for the UK winter flu vaccines.
Boots are now taking bookings for the UK winter flu vaccines.
fapumpkin
in
CLL Support
7 days ago
Blood in urine/uti symptoms but no infection
I'm currently in a flare up, following a hysterectomy nearly 5 months ago for Fibroids and Adenomyosis. They now think I have Occult endometriosis, as my pelvic pain has flared up again since starting hrt. Ive been referred to a bsge centre.My bladder symptoms are awful I feel like I have a raging uti
I'm currently in a flare up, following a hysterectomy nearly 5 months ago for Fibroids and Adenomyosis. They now think I have Occult endometriosis, as my pelvic pain has flared up again since starting hrt. Ive been referred to a bsge centre.My bladder symptoms are awful I feel like I have a raging uti
Mindfullness4791
in
Endometriosis UK
8 days ago
Saw Cardiologist today, now more anxious than ever.
Hi Everyone Thank you all for your lovely replies to my original post. I saw the cardiologist today and he says he thinks my PH is primarily caused by my asthma/COPD. He didn't put me on any medications at this stage. He wants an ultra sound done on my heart in September [[2 months away!] to compare
Hi Everyone Thank you all for your lovely replies to my original post. I saw the cardiologist today and he says he thinks my PH is primarily caused by my asthma/COPD. He didn't put me on any medications at this stage. He wants an ultra sound done on my heart in September [[2 months away!] to compare
puddy68
in
Lung Conditions Community Forum
9 days ago
Cold Turkey
Hello Everyone, What happens if i just "Cold Turkey" Stop the 6.5 mg of methylprednisolone? I'm so sick of it all. I've gotten very low on meds (even zero for a few days) and the pain and stiffness return so bad i can't function. If i just quit, what's the worst that can happen?
Hello Everyone, What happens if i just "Cold Turkey" Stop the 6.5 mg of methylprednisolone? I'm so sick of it all. I've gotten very low on meds (even zero for a few days) and the pain and stiffness return so bad i can't function. If i just quit, what's the worst that can happen?
ifeelold
in
PMRGCAuk
11 days ago
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