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stage 3b/c inoperable non small cell lung cancer. Cannot tolerate durvalumab, (pneumonitis) No mutations - any hope?
hi, Im 57 and was diagnosed with inoperable non small cell lung cancer in October 2022. Since then Ive adopted a dairy, gluten & sugar free diet , organic only & prinipally vegan. I take millions of supplements a day plus Chinese traditional Medicine. I’ve had 3 rounds of chemo, then combined radio
hi, Im 57 and was diagnosed with inoperable non small cell lung cancer in October 2022. Since then Ive adopted a dairy, gluten & sugar free diet , organic only & prinipally vegan. I take millions of supplements a day plus Chinese traditional Medicine. I’ve had 3 rounds of chemo, then combined radio
ohayeai
in
The Roy Castle Lung Cancer Foundation
5 months ago
EP consult
The cardiologist I see is not able to provide medical management of my paroxysmal afib due to my low heart rate and low blood pressure (can't risk pushing either value lower), so I am hoping for an ablation. This morning, due to a cancellation, I was able to bring my initial EP consult forward by 1
The cardiologist I see is not able to provide medical management of my paroxysmal afib due to my low heart rate and low blood pressure (can't risk pushing either value lower), so I am hoping for an ablation. This morning, due to a cancellation, I was able to bring my initial EP consult forward by 1
Desertflowerchild
in
Atrial Fibrillation Support
5 months ago
perimenopause and heart stuff!
at 49 I’ve finally realised the not sleeping and feeling head fog for the past years is not having a late child (7 now) and a stent (1.5 now), it’s perimenpause as I’m now getting a lot of hot flushes (heat not helping here!). Periods still normal if closer together. But I’ve also being having more
at 49 I’ve finally realised the not sleeping and feeling head fog for the past years is not having a late child (7 now) and a stent (1.5 now), it’s perimenpause as I’m now getting a lot of hot flushes (heat not helping here!). Periods still normal if closer together. But I’ve also being having more
Mangojamontoast
in
British Heart Foundation
11 months ago
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Zoladex and HRT
Spoke to surgeonSo my surgeon rang yesterday and explained why they aborted the hysterectomy on Tuesday. He said my cervix was fused to my bowel and possibly left ovary and my rectum had been pulled down too. He said it looked to be endometriosis that had been there a long, long time and they wouldn't
Spoke to surgeonSo my surgeon rang yesterday and explained why they aborted the hysterectomy on Tuesday. He said my cervix was fused to my bowel and possibly left ovary and my rectum had been pulled down too. He said it looked to be endometriosis that had been there a long, long time and they wouldn't
Sunset-lady
in
Endometriosis UK
11 months ago
coming off oxicodone
Despite the victorious stopping of my RLS, i am still struggling with sleep. I have been taking 10mg of oxicodone. One dose at night. But it had been making me dog tired and zombie like during day. I have read lots on here about spreading the dose but i want to come off it. I am starting to cut it down
Despite the victorious stopping of my RLS, i am still struggling with sleep. I have been taking 10mg of oxicodone. One dose at night. But it had been making me dog tired and zombie like during day. I have read lots on here about spreading the dose but i want to come off it. I am starting to cut it down
Jukebox55
in
Restless Legs Syndrome
11 months ago
Things, regimens,etc that are probably RLS worthless.
THINGS THAT DO NOT WORK FOR RLS All of us with RLS/PLMD have slightly different symptoms. We have tried various 'remedies' to try to relieve our RLS symptoms. We have read articles, some interesting, some ridiculous (bar of soap) that make amazing promises. And there is an entire array of things to
THINGS THAT DO NOT WORK FOR RLS All of us with RLS/PLMD have slightly different symptoms. We have tried various 'remedies' to try to relieve our RLS symptoms. We have read articles, some interesting, some ridiculous (bar of soap) that make amazing promises. And there is an entire array of things to
fritz34
in
Restless Legs Syndrome
5 months ago
Wrist Ulna Head Joint Replacement
Has anyone had their wrist ulna head joint replaced due to RA and if so, how are you doing now?
Has anyone had their wrist ulna head joint replaced due to RA and if so, how are you doing now?
ellilu58
in
NRAS
8 months ago
Fragility score on Osteoscan and different meds.
Hello to “my turn to” friends. This is a new one to me.I had an osteoscan, my second. The last one was nearly two years ago. Since then I have had a Thr for Avascular necrosis and I am still struggling along dealing with flares after eight years. I have been on Leflunomide for two months now. Tapering
Hello to “my turn to” friends. This is a new one to me.I had an osteoscan, my second. The last one was nearly two years ago. Since then I have had a Thr for Avascular necrosis and I am still struggling along dealing with flares after eight years. I have been on Leflunomide for two months now. Tapering
Nightingales
in
PMRGCAuk
11 months ago
ONLINE SUPPORT GROUPS
Our support groups are such a good way to connect with other's in a similar situation, they have really helped so many people make friendships and gain valuable knowledge around their treatment and care. If you have any queries about anything please get in touch, we would love to hear from you and help
Our support groups are such a good way to connect with other's in a similar situation, they have really helped so many people make friendships and gain valuable knowledge around their treatment and care. If you have any queries about anything please get in touch, we would love to hear from you and help
ConnectRoyCastle
Administrator
in
The Roy Castle Lung Cancer Foundation
6 months ago
Another update
This is just a reply (edited), not an original post but readers may find it of interest. As far as I know all replies are public and can be viewed by any Enc. member. "To know we are still useful despite our disability is a big bonus. I used to open the curtains on the ward and make my own bed and the
This is just a reply (edited), not an original post but readers may find it of interest. As far as I know all replies are public and can be viewed by any Enc. member. "To know we are still useful despite our disability is a big bonus. I used to open the curtains on the ward and make my own bed and the
Gandalf2
in
Encephalitis International
6 months ago
Abiraterone + Olaparib: ASCO GU 2024 Highlights: BRCAAway Trial
"Highlighting the trial's results, he notes the combination therapy significantly extended median radiographic progression-free survival to 39 months, far surpassing the outcomes with either treatment alone. " 39 months progression free is not bad at all... https://www.urotoday.com/video-lectures/asco-gu
"Highlighting the trial's results, he notes the combination therapy significantly extended median radiographic progression-free survival to 39 months, far surpassing the outcomes with either treatment alone. " 39 months progression free is not bad at all... https://www.urotoday.com/video-lectures/asco-gu
Maxone73
in
Advanced Prostate Cancer
6 months ago
Women are not taken seriously by most doctors when experiencing health problems.
I went through a really rough time a couple of years after I had my first child when I was about 31 years old. I had never experienced PMT prior to the birth. I was lucky. However, I became aware of gradual fatigue, and anxiety, and hot flushes. I went to my GP to ask if I could be going through the
I went through a really rough time a couple of years after I had my first child when I was about 31 years old. I had never experienced PMT prior to the birth. I was lucky. However, I became aware of gradual fatigue, and anxiety, and hot flushes. I went to my GP to ask if I could be going through the
DandyButch
in
Thyroid UK
11 months ago
Do I need to stop taking estrogen? Feel as if I'm choosing between mental and physical health.
So I've read a lot now- probably too much. From what I can gather from things (and I am new to this - didnt know I had endometriosis until Tuesday when they aborted my hysterectomy as my bowel is fused to my cervix) estrogen seems to be the driving force behind endometriosis. Is that true? It also seems
So I've read a lot now- probably too much. From what I can gather from things (and I am new to this - didnt know I had endometriosis until Tuesday when they aborted my hysterectomy as my bowel is fused to my cervix) estrogen seems to be the driving force behind endometriosis. Is that true? It also seems
Sunset-lady
in
Endometriosis UK
11 months ago
Over range copper and zinc
The only culprit I can think of is milk thistle. Any thoughts on over range copper and zinc? About a 10 months ago, zinc was low-ish and copper slightly over so I supplemented zinc for a short while but stopped a couple of months ago. Then the week before last started with milk thistle for liver support
The only culprit I can think of is milk thistle. Any thoughts on over range copper and zinc? About a 10 months ago, zinc was low-ish and copper slightly over so I supplemented zinc for a short while but stopped a couple of months ago. Then the week before last started with milk thistle for liver support
Noelnoel
in
Thyroid UK
11 months ago
T3-4-Hypo trial - Netherlands
Do view the original which includes a map and various links. 16 to 20 months is so much more sensible than the few weeks so many previous studies have been based on. [i]
T3-4-Hypo trial
[/i] [i]Updated on 25 January 2024[/i] [i]CALL – study T3 / T4 combination therapy[/i] [i]In most patients
Do view the original which includes a map and various links. 16 to 20 months is so much more sensible than the few weeks so many previous studies have been based on. [i]
T3-4-Hypo trial
[/i] [i]Updated on 25 January 2024[/i] [i]CALL – study T3 / T4 combination therapy[/i] [i]In most patients
helvella
Thyroid UK
in
Thyroid UK
6 months ago
Gene therapy
TOP TAKEAWAYSGene therapy has a potential place In the treatment • of Parkinson disease, but won't be the "be all end al as some may think. There are a lot of questions regarding drug development of PD gene therapies, Including which targets are the most promlslng/effectlve. Investlgatlonal right now
TOP TAKEAWAYSGene therapy has a potential place In the treatment • of Parkinson disease, but won't be the "be all end al as some may think. There are a lot of questions regarding drug development of PD gene therapies, Including which targets are the most promlslng/effectlve. Investlgatlonal right now
Farooqji
in
Cure Parkinson's
6 months ago
Lupron unjection not reducing PSA
I was first diagnosed with prostate cancer in 2016. It has been contained in the prostate ever since. For 3 years I treated myself with vitamins and nutrients. Kept my psa down until I had a kidney stone operation and for some odd ball reason loss control of the psa after the operation, it shot up to
I was first diagnosed with prostate cancer in 2016. It has been contained in the prostate ever since. For 3 years I treated myself with vitamins and nutrients. Kept my psa down until I had a kidney stone operation and for some odd ball reason loss control of the psa after the operation, it shot up to
woppaginny
in
Advanced Prostate Cancer
6 months ago
Min invasive Aortic valve replacement:- happy or disappointed?
I’m 67 yo, male, slightly overweight but otherwise good health but I have a severe Aortic Stenosis, that’s running at about 25% of full capacity. My only symptoms are slight breathlessness when climbing stairs. Saw a surgeon yesterday who wants to replace the valve with an animal valve, but he does not
I’m 67 yo, male, slightly overweight but otherwise good health but I have a severe Aortic Stenosis, that’s running at about 25% of full capacity. My only symptoms are slight breathlessness when climbing stairs. Saw a surgeon yesterday who wants to replace the valve with an animal valve, but he does not
7LTR
in
British Heart Foundation
8 months ago
testing protocol on T4 and T3
Hi all. Does anyone have any experience/wisdom re a good time to take T3 pre bloods? I currently take it when I wake up which is between 6.20 and 7.30 and in the afternoon between 3.30 and 4.30. I have a first test since starting combined therapy booked and am wondering when I should take what.
Hi all. Does anyone have any experience/wisdom re a good time to take T3 pre bloods? I currently take it when I wake up which is between 6.20 and 7.30 and in the afternoon between 3.30 and 4.30. I have a first test since starting combined therapy booked and am wondering when I should take what.
Topes009
in
Thyroid UK
6 months ago
think I’ve found my trigger.
I have posted on here before asking for advice. Have always suffered on and off but the last 18 months have been awful. Saw a dctr last year who just gave me sleeping tablets, saw a dctr a few weeks ago who gave me pramipexole but after reading on here and other sites about the side effects decided
I have posted on here before asking for advice. Have always suffered on and off but the last 18 months have been awful. Saw a dctr last year who just gave me sleeping tablets, saw a dctr a few weeks ago who gave me pramipexole but after reading on here and other sites about the side effects decided
Patters56
in
Restless Legs Syndrome
11 months ago
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