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My brother has advanced Prostate Cancer
I'm here for my brother. He is 55 now. He has diagnosed when he was 54 with advanced prostate cancer that had metastasized to his pelvic bone. He started hormone therapy on October 2022 and then started chemotherapy for 6 sessions from November 2022 till March 2023 and started Nubeqa at the same time
I'm here for my brother. He is 55 now. He has diagnosed when he was 54 with advanced prostate cancer that had metastasized to his pelvic bone. He started hormone therapy on October 2022 and then started chemotherapy for 6 sessions from November 2022 till March 2023 and started Nubeqa at the same time
rasher1
in
Advanced Prostate Cancer
8 months ago
Starting Abiraterone and predniSONE
Tomorrow morning I take my first dose of Abiraterone (Zytiga) and predniSONE for metastatic castrate resistant prostate cancer. I don't know what kind of side effects I would get. I hope I would tolerate the treatment well. Reaching this stage of my cancer I reflect on my 12 year journey with prostate
Tomorrow morning I take my first dose of Abiraterone (Zytiga) and predniSONE for metastatic castrate resistant prostate cancer. I don't know what kind of side effects I would get. I hope I would tolerate the treatment well. Reaching this stage of my cancer I reflect on my 12 year journey with prostate
dac500
in
Advanced Prostate Cancer
8 months ago
Vitamin D
I have it prescribed once a week D3 ( CLL & Multiple Sclerosis
I have it prescribed once a week D3 ( CLL & Multiple Sclerosis
Marco54
in
CLL Support
5 months ago
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home from cardioversion
so I had my 2nd cardioversion today, first one lasted over 2 years……so hopefully this one will last a fair while too. Only took one zap and I was back in sinus rhythm. This time I’ve been told to continue my bisoprolol but last time I wasn’t on them at all. Hopefully this wil keep me in sync until I
so I had my 2nd cardioversion today, first one lasted over 2 years……so hopefully this one will last a fair while too. Only took one zap and I was back in sinus rhythm. This time I’ve been told to continue my bisoprolol but last time I wasn’t on them at all. Hopefully this wil keep me in sync until I
Fondant
in
AF Association
4 months ago
Legal Advice?
Hi All, Although this post is not MS-related, I wanted to reach out to my MSAA Community for their input. Perhaps someone here can point me in the right direction, as I don't really have the money to hire an attorney. Unfortunately, this situation doesn't lend itself to any "free advice and/or attorneys
Hi All, Although this post is not MS-related, I wanted to reach out to my MSAA Community for their input. Perhaps someone here can point me in the right direction, as I don't really have the money to hire an attorney. Unfortunately, this situation doesn't lend itself to any "free advice and/or attorneys
DM0329
in
My MSAA Community
8 months ago
Research Lounge FREE Online Event: Does knowledge of liver scarring affect drinking behaviour?
Does knowing the effects of alcohol on your liver change your drinking?
Researchers have been looking at how people's drinking behaviours may change when they know that alcohol is damaging their liver. They have some interesting and thought-provoking results to share with you on:
Wednesday
Does knowing the effects of alcohol on your liver change your drinking?
Researchers have been looking at how people's drinking behaviours may change when they know that alcohol is damaging their liver. They have some interesting and thought-provoking results to share with you on:
Wednesday
BritishLiverTrust1
Partner
in
British Liver Trust
8 months ago
Multiple mechanisms to clear a-synuclein with natural substances (in mice).
For informational purposes only Alpha Synuclein 1. INTRODUCTION: There are no effective treatments nor drugs available to modify disease progression
For informational purposes only Alpha Synuclein 1. INTRODUCTION: There are no effective treatments nor drugs available to modify disease progression
House2
in
Cure Parkinson's
8 months ago
Scientists have discovered a new cause of Parkinsons disease
https://scitechdaily.com/scientists-have-discovered-a-new-cause-of-parkinsons-disease/ A major discovery sheds light on the underlying mechanisms of Parkinson’s disease, opening the door for novel therapeutic approaches down the line. Until recently, our understanding of Parkinson’s disease has been
https://scitechdaily.com/scientists-have-discovered-a-new-cause-of-parkinsons-disease/ A major discovery sheds light on the underlying mechanisms of Parkinson’s disease, opening the door for novel therapeutic approaches down the line. Until recently, our understanding of Parkinson’s disease has been
NextStage
in
Cure Parkinson's
8 months ago
RA in jaw
hi,has anyone experienced stiffness in their jaw when you open and close your mouth that a bit painful? I have rheumatoid arthritis and I think it keeps going into my jaw!!has anyone got any advice? Thanks!!👍
hi,has anyone experienced stiffness in their jaw when you open and close your mouth that a bit painful? I have rheumatoid arthritis and I think it keeps going into my jaw!!has anyone got any advice? Thanks!!👍
Mybirthday1975
in
NRAS
5 months ago
Atrial Fibrillation Association Patients Day On-Demand now!
Is your .... Heart racing? Palpitations? Breathlessness? How do you manage living with AF? Join us from the comfort of your home to hear from medical experts in AF. You will be able to manage living with AF so much better after watching these presentations. To view the agenda and register
Is your .... Heart racing? Palpitations? Breathlessness? How do you manage living with AF? Join us from the comfort of your home to hear from medical experts in AF. You will be able to manage living with AF so much better after watching these presentations. To view the agenda and register
TracyAdmin
Partner
in
AF Association
4 months ago
Heavy legs and low energy feeling
My recent thyroid results showed a below range T3, and I have been having trouble with a brand of thyroxine and feeling generally unwell as previously posted with some helpful advice. But, I have a feeling of heavy legs and low energy and wondered whether when the T3 is low it can cause this? I am
My recent thyroid results showed a below range T3, and I have been having trouble with a brand of thyroxine and feeling generally unwell as previously posted with some helpful advice. But, I have a feeling of heavy legs and low energy and wondered whether when the T3 is low it can cause this? I am
Sailing14
in
Thyroid UK
8 months ago
Home Oxygen is a game changer
Afternoon all! Mindful that it has been a fair while since my last post - much longer than intended. However, in many ways it's a good thing as it means I've got more to update you all on. First and foremost, I'm still on the lung transplant list and have yet to get another call since being re-added
Afternoon all! Mindful that it has been a fair while since my last post - much longer than intended. However, in many ways it's a good thing as it means I've got more to update you all on. First and foremost, I'm still on the lung transplant list and have yet to get another call since being re-added
dodgylungrunner
British Lung Foundation
in
Lung Conditions Community Forum
1 year ago
lesley
I have been diagnosed with an underactive thyroid. I do suffer with bad anxiety & it’s been getting worse over the last year. Can taking thyroxine help the anxiety as I’m living on adrenaline!!! im told it dores help. Anyone else had this?
I have been diagnosed with an underactive thyroid. I do suffer with bad anxiety & it’s been getting worse over the last year. Can taking thyroxine help the anxiety as I’m living on adrenaline!!! im told it dores help. Anyone else had this?
Lesley2357
in
Anxiety Support
5 months ago
Do you live with advanced liver disease? Are you interested in attending an in-person workshop in Bristol or Liverpool this month?
The British Liver Trust are working with UK CLIF, a dynamic new network of clinicians, patients, carers/relatives and researchers coming together over our shared interest to improve research and clinical outcomes for people with chronic liver failure. Cases of liver disease are rising alarmingly and
The British Liver Trust are working with UK CLIF, a dynamic new network of clinicians, patients, carers/relatives and researchers coming together over our shared interest to improve research and clinical outcomes for people with chronic liver failure. Cases of liver disease are rising alarmingly and
BritishLiverTrust1
Partner
in
British Liver Trust
8 months ago
Not PMR
I have been told that I don't have PMR from my rheumatologist but rheumatoid arthritis so must I leave this invaluable site and find one more suitable for my ailment? If so I will be sorry to miss my family of helpers.
I have been told that I don't have PMR from my rheumatologist but rheumatoid arthritis so must I leave this invaluable site and find one more suitable for my ailment? If so I will be sorry to miss my family of helpers.
Petertaffy
in
PMRGCAuk
5 months ago
travelling as Lupus patient
hi everyone, Been long time since I wrote here. please I will like some advice regarding travelling in Africa. I have been here in Europe for over 15 years and I haven’t been to Africa all this years. Was diagnosed with lupus 2018 in Italy. I wanted to ask for any advice on sun cream and any
hi everyone, Been long time since I wrote here. please I will like some advice regarding travelling in Africa. I have been here in Europe for over 15 years and I haven’t been to Africa all this years. Was diagnosed with lupus 2018 in Italy. I wanted to ask for any advice on sun cream and any
Saralife
in
LUPUS UK
5 months ago
new members
I know all too well how overwhelming this diagnosis can be to anyone. All of the emotions that can follow are hard to deal with for sure. If any new member doesn't feel comfortable posting anything here initially, please feel free to send me a message via 'chat'. We have all been exactly where you
I know all too well how overwhelming this diagnosis can be to anyone. All of the emotions that can follow are hard to deal with for sure. If any new member doesn't feel comfortable posting anything here initially, please feel free to send me a message via 'chat'. We have all been exactly where you
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
Ectopic atrial Bradycardia
My last ECG before I saw EP said that Ectopic atrial Bradycardia treatment shad replaced Afib . I have an ablation scheduled end of month and he didn’t say anything about this? Does anyone have the same thing? I had a cardio version Sept and small Afib Nov but way overdue now for an Afib and wondering
My last ECG before I saw EP said that Ectopic atrial Bradycardia treatment shad replaced Afib . I have an ablation scheduled end of month and he didn’t say anything about this? Does anyone have the same thing? I had a cardio version Sept and small Afib Nov but way overdue now for an Afib and wondering
Krissy55
in
Atrial Fibrillation Support
5 months ago
PSMA pet scan negative
My PSA was 0.1 on july 17th and 0.3 on Oct 16th. PSMA scan was done on Nov 7th but was negative. Am I safe to assume there must be some prostate cancer cell present that are not showing up on the scan? I am meeting with my MO at Dana Farber next week Any suggestions moving forward? I appreciate the
My PSA was 0.1 on july 17th and 0.3 on Oct 16th. PSMA scan was done on Nov 7th but was negative. Am I safe to assume there must be some prostate cancer cell present that are not showing up on the scan? I am meeting with my MO at Dana Farber next week Any suggestions moving forward? I appreciate the
Rfs1975
in
Advanced Prostate Cancer
8 months ago
Behcets + Personal Independence Payment (UK)
I have relatively mild behcets syndrome (frequent mouth ulcers, joint swelling are the main symptoms but there have been periods where i have been unable to walk) Has anyone UK based living with the disease been able to claim
Personal Independence Payment? I'm quite tired of having to pay for my
I have relatively mild behcets syndrome (frequent mouth ulcers, joint swelling are the main symptoms but there have been periods where i have been unable to walk) Has anyone UK based living with the disease been able to claim
Personal Independence Payment? I'm quite tired of having to pay for my
jaquarius
in
Behçet's UK
8 months ago
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