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Gaucher disease type 3 (GD3)
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Do low PSA-producing cells still rely on testosterone to grow?
Am curious to know what the folks here know about this question. If higher PSA cells are driven to near extinction by ADT, and if only low-PSA producing cells survive, are the latter still dependent on testosterone for survival? If not, what do they depend on to grow?
Am curious to know what the folks here know about this question. If higher PSA cells are driven to near extinction by ADT, and if only low-PSA producing cells survive, are the latter still dependent on testosterone for survival? If not, what do they depend on to grow?
novatimo
in
Advanced Prostate Cancer
7 months ago
Do you know your pulse?
Your heartbeat is the most fundamental rhythm in your life, signalling the regular pumping of your heart as it propels blood carrying oxygen and nutrients to the rest of your body. We take the regular beating completely for granted, never giving it a second thought until the elegant control process
Your heartbeat is the most fundamental rhythm in your life, signalling the regular pumping of your heart as it propels blood carrying oxygen and nutrients to the rest of your body. We take the regular beating completely for granted, never giving it a second thought until the elegant control process
TracyAdmin
Partner
in
Sudden Cardiac Arrest & Heart Attack
2 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
4 months ago
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change of medication to Atenolol from Bisoprolol
I have been on Bisoprolol for a couple of weeks but I haven’t felt great. I felt tired and foggy most of the time, struggled to get my breath and my feet were freezing. I have spoken to the pharmacist at our surgery and he has changed my medication to Atenolol even though he said Bisoprolol was the preferred
I have been on Bisoprolol for a couple of weeks but I haven’t felt great. I felt tired and foggy most of the time, struggled to get my breath and my feet were freezing. I have spoken to the pharmacist at our surgery and he has changed my medication to Atenolol even though he said Bisoprolol was the preferred
Wilky57
in
Atrial Fibrillation Support
2 months ago
Persistent AF
Hello, for the past couple of years I have had paroxysmal AF which has taken increasingly long times to convert to NSR. The last few have been 22 hours and usually every couple of weeks or so. This time I was quite pleased as I went 22 days without, the longest interval for 18 months. However it's now
Hello, for the past couple of years I have had paroxysmal AF which has taken increasingly long times to convert to NSR. The last few have been 22 hours and usually every couple of weeks or so. This time I was quite pleased as I went 22 days without, the longest interval for 18 months. However it's now
Spj57
in
Atrial Fibrillation Support
2 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
4 months ago
Endo gave me private prescription
so, good news! The private Endo appointment went as I’d hoped and he was happy to let me try T3. I’m now trying to source it. I’ve had a no back from a couple of places on the list from Thyroid UK. Thing is, I just wanted to check as on the prescription it says triiodothyronine rather than liothyronine
so, good news! The private Endo appointment went as I’d hoped and he was happy to let me try T3. I’m now trying to source it. I’ve had a no back from a couple of places on the list from Thyroid UK. Thing is, I just wanted to check as on the prescription it says triiodothyronine rather than liothyronine
Loopnova
in
Thyroid UK
2 months 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
4 months ago
Selbourn
Two weeks ago I was given, what the Rummy called a maintenance dose, of Rituximab and of course 125mg of prednisone first. All good apart from little sleep after the Pred! But now OK but very tired all the time could be the ANCA or the meds who knows. I am also having very vivid bad dreams, is anyone
Two weeks ago I was given, what the Rummy called a maintenance dose, of Rituximab and of course 125mg of prednisone first. All good apart from little sleep after the Pred! But now OK but very tired all the time could be the ANCA or the meds who knows. I am also having very vivid bad dreams, is anyone
Selbourn
in
Vasculitis UK
2 months ago
Forum Updates from 29 February 2024
Hello I would like to share the news with you all that our Charity Forums have recently been rebranded and renamed to reflect the condition to which each Forum provides information and support with. The Health Unlocked Team have assured us that all existing members will be unaffected by these changes
Hello I would like to share the news with you all that our Charity Forums have recently been rebranded and renamed to reflect the condition to which each Forum provides information and support with. The Health Unlocked Team have assured us that all existing members will be unaffected by these changes
TracyAdmin
ArrhythmiaAlliance
in
Heart Rhythm Disorders Support
2 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
4 months ago
Moderate Calcification
Good morning all, I was recently invited for a lung check and have been recalled as the scan showed moderate Calcification. As I like to be proactive and believe this is due to fatty diet, are there any recommendations for menus that will halt (improve?) This condition. My brother dies with this condition
Good morning all, I was recently invited for a lung check and have been recalled as the scan showed moderate Calcification. As I like to be proactive and believe this is due to fatty diet, are there any recommendations for menus that will halt (improve?) This condition. My brother dies with this condition
1AnneMcC
in
Healthy Eating
2 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
4 months ago
Post Amiodarone and waiting for ablation
I was on Amiodarone for 12 months after diagnosis of persistent AF post Covid and stopped taking it in October '23. I had a cardioversion in June and as far as I'm aware I'm still in sinus rhythm. I'm on the list for an ablation at the John Radcliffe in Oxford. I had a couple of blood tests, at my
I was on Amiodarone for 12 months after diagnosis of persistent AF post Covid and stopped taking it in October '23. I had a cardioversion in June and as far as I'm aware I'm still in sinus rhythm. I'm on the list for an ablation at the John Radcliffe in Oxford. I had a couple of blood tests, at my
JoDogBlue
in
Atrial Fibrillation Support
2 months ago
Pressure onback causing AF
I lay on my left side today and nasty afib came on within a couple minutes same on back. I then tried lying on right side and i felt ok with my EMAY ecg saying bradycardia. I qent to GP and she will book me in for xray back and front.Colin
I lay on my left side today and nasty afib came on within a couple minutes same on back. I then tried lying on right side and i felt ok with my EMAY ecg saying bradycardia. I qent to GP and she will book me in for xray back and front.Colin
Alphakiwi
in
Atrial Fibrillation Support
2 months ago
What I had failed to grasp about caffeine all these years...
I am a coffee lover all the way through my life to the extent that we now have a nespresso these days with all the various blends to keep variety up. All the research I read talked about the anti-oxidant properties of coffee and the benefits to a more positive digestion etc etc. Even I used to think
I am a coffee lover all the way through my life to the extent that we now have a nespresso these days with all the various blends to keep variety up. All the research I read talked about the anti-oxidant properties of coffee and the benefits to a more positive digestion etc etc. Even I used to think
Danielj1
in
Thyroid UK
7 months ago
multaq and increased heart beat
Hi everyone haven’t posted for a while,but reading the site daily. Had my third ablation in October 2023 mostly for atypical flutter,procedure wasn’t long but quite extensive judging from post procedure troponin elevations over 20,000.Placed on Multaq afterwards as I already failed all other meds and
Hi everyone haven’t posted for a while,but reading the site daily. Had my third ablation in October 2023 mostly for atypical flutter,procedure wasn’t long but quite extensive judging from post procedure troponin elevations over 20,000.Placed on Multaq afterwards as I already failed all other meds and
55zuzanka61
in
AF Association
2 months ago
eye sight affected with af
hello again to all, been off the site for a long while but like to check in now and again. My af usually only lasts a few seconds several times a day but I do get what I call bad episodes where it really affects my daily life I.e very tired more than a fair bit. The other night while moving from settee
hello again to all, been off the site for a long while but like to check in now and again. My af usually only lasts a few seconds several times a day but I do get what I call bad episodes where it really affects my daily life I.e very tired more than a fair bit. The other night while moving from settee
rubble4356
in
AF Association
2 months ago
Lynne
Hi,My name is Lynne and I am new to the Forum and to Asthma! Looking back I have been breathless going up two flights of stairs at home for a while,but another respiratory virus in November left me with fatigue,cough and breathlessness. My G.P started me on inhalers while waiting for a Spiro test.
Hi,My name is Lynne and I am new to the Forum and to Asthma! Looking back I have been breathless going up two flights of stairs at home for a while,but another respiratory virus in November left me with fatigue,cough and breathlessness. My G.P started me on inhalers while waiting for a Spiro test.
Budd1ngart1st
in
Asthma Community Forum
2 months ago
Thunking of getting an orchiectomy insted od radiation
Has anyone had an orchiectomy and if so how were your side effects and how is your life after the Big O.I'm scheduled to start Full Pelvic Radiation in 6 weeks but fear the long term side effects. I asked if anyone here had FPR and if so what were their side effects and life like since then. Thanks for
Has anyone had an orchiectomy and if so how were your side effects and how is your life after the Big O.I'm scheduled to start Full Pelvic Radiation in 6 weeks but fear the long term side effects. I asked if anyone here had FPR and if so what were their side effects and life like since then. Thanks for
woppaginny
in
Advanced Prostate Cancer
7 months ago
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