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Back again!!
I have been on here a few times and Jools and Sue saved my sanity! Other's have also been so kind so, thank you...again! I do have another question which I'm sure Jools and Sue can help me with. The 20 mcg Buprenorphine patch has helped my RLS hugely though I know it's lurking but I can now sleep which
I have been on here a few times and Jools and Sue saved my sanity! Other's have also been so kind so, thank you...again! I do have another question which I'm sure Jools and Sue can help me with. The 20 mcg Buprenorphine patch has helped my RLS hugely though I know it's lurking but I can now sleep which
Danni54
in
Restless Legs Syndrome
5 months ago
Prostatitis advice
My partner (in his mid 60s) had prostate biopsies (over 60 samples) done in summer 2023. He needed a catheter for many weeks afterwards and was in a lot of pain and passing many blood clots. Over the last year since the biopsies he's had recurrent bouts of slow and intermittent urine flow, now having
My partner (in his mid 60s) had prostate biopsies (over 60 samples) done in summer 2023. He needed a catheter for many weeks afterwards and was in a lot of pain and passing many blood clots. Over the last year since the biopsies he's had recurrent bouts of slow and intermittent urine flow, now having
ConcernedOtherHalf
in
Men's Health Forum
11 months ago
looking for a neurologist
Can anyone recommend a neurologist knowledgeable in RLS in the Bristol/ Bath (England) area ? I currently have a neurologist whom I rate quite highly but who cannot prescribe opioids as they are not on the formulary of the hospital where she practises. She has however asked my GP to prescribe Oxycodone
Can anyone recommend a neurologist knowledgeable in RLS in the Bristol/ Bath (England) area ? I currently have a neurologist whom I rate quite highly but who cannot prescribe opioids as they are not on the formulary of the hospital where she practises. She has however asked my GP to prescribe Oxycodone
etchea33
in
Restless Legs Syndrome
5 months ago
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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
The "other" symptoms of PMR?
I was diagnosed with PMR in July 2022 after 2 months of sudden onset of symptoms. I was very fit & healthy at time of first symptoms. I am using DSNS weaning regime & down to 7mg & had 2 flares during this time. Currently stuck on 7mg for a month due to slight hip discomfort. My question is less
I was diagnosed with PMR in July 2022 after 2 months of sudden onset of symptoms. I was very fit & healthy at time of first symptoms. I am using DSNS weaning regime & down to 7mg & had 2 flares during this time. Currently stuck on 7mg for a month due to slight hip discomfort. My question is less
Flinders61
in
PMRGCAuk
1 year ago
Inflammatory Pain and T
I have had T for over two years now following an attack of vertigo with varying diagnoses of labyrinthitis, bppv or vestibular neuritis, none of which have ever been confirmed.. and after all this time I feel stuck with no sign of reaching habituation.. I had months of complaining of a dullness in my
I have had T for over two years now following an attack of vertigo with varying diagnoses of labyrinthitis, bppv or vestibular neuritis, none of which have ever been confirmed.. and after all this time I feel stuck with no sign of reaching habituation.. I had months of complaining of a dullness in my
Shozza1
in
Tinnitus 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
Spontaneous remission of some blood counts after Dx
This just is a question of curiosity I've discussed briefly before. If any members have seen something like this it would be interesting to know. I've asked two MPN Drs about it and all I hear is "it's complicated" and/or "things fluctuate". -- These plots show some counts and when I started aspirin
This just is a question of curiosity I've discussed briefly before. If any members have seen something like this it would be interesting to know. I've asked two MPN Drs about it and all I hear is "it's complicated" and/or "things fluctuate". -- These plots show some counts and when I started aspirin
EPguy
in
MPN Voice
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
7 days 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)
8 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
9 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
11 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)
12 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
13 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
14 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
15 days 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
6 months 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
17 days ago
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