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Selegiline side effects
Hi All. Due to drug shortages we've been unable to get rasagiline and had to swap to selegiline. Since the swap mum has had lots of unusual bleeding and the GP thinks it may be a side effect of the selegiline. Just wondered if anyone else has had similar problems and if so how did you resolve things?
Hi All. Due to drug shortages we've been unable to get rasagiline and had to swap to selegiline. Since the swap mum has had lots of unusual bleeding and the GP thinks it may be a side effect of the selegiline. Just wondered if anyone else has had similar problems and if so how did you resolve things?
Joluu
in
PSP Association
8 months ago
PSA went up after three treatments of chemotherapy
I have had 3 Chemotherapy treatments with Docataxel. before the first treatment PSA was 89. after the first treatment PSA was 73.31.. after the second treatment PSA was 52.82. after the third treatment, PSA was 73.31.. does it make sense to take another chemotherapy treatment since the PSA has risen
I have had 3 Chemotherapy treatments with Docataxel. before the first treatment PSA was 89. after the first treatment PSA was 73.31.. after the second treatment PSA was 52.82. after the third treatment, PSA was 73.31.. does it make sense to take another chemotherapy treatment since the PSA has risen
spolyu
in
Advanced Prostate Cancer
8 months ago
It's Back!
This post should be good for newbies also. This should show you guys how long you can go!Anyways, 13 years ago I was diagnosed with PCA Gleason 7 PSA 44. With spread outside of prostate. Did 39 treatments off radiation and have been mostly on ADT for the duration except during COVID I took a break
This post should be good for newbies also. This should show you guys how long you can go!Anyways, 13 years ago I was diagnosed with PCA Gleason 7 PSA 44. With spread outside of prostate. Did 39 treatments off radiation and have been mostly on ADT for the duration except during COVID I took a break
Tjc1
in
Advanced Prostate Cancer
8 months ago
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Vitamin B supplements
I recently posted my iron test results which were on the high side and therefore I didn't need to supplement and if possible I should try to bring my levels down. I am about to start taking Vitamin B supplements based on a Blue Horizon thyroid test. My question is - will B supplements increase my iron
I recently posted my iron test results which were on the high side and therefore I didn't need to supplement and if possible I should try to bring my levels down. I am about to start taking Vitamin B supplements based on a Blue Horizon thyroid test. My question is - will B supplements increase my iron
sabby-c
in
Thyroid UK
25 days ago
Covid Injections for April 2024
Hi Everyone. Has anybody received a letter yet about their April Covid jab? You follow the NHS App and it brings up an out of date link telling you about Autumn 2023 jabs. It then tells you further down that the page will be updated in 2026. I just looked on my personal NHS account and nowhere can
Hi Everyone. Has anybody received a letter yet about their April Covid jab? You follow the NHS App and it brings up an out of date link telling you about Autumn 2023 jabs. It then tells you further down that the page will be updated in 2026. I just looked on my personal NHS account and nowhere can
Blackwitch
in
NRAS
6 months ago
Vitamin B12
In addition to my daily Thyroxine dose of 100mcg I have been prescribed Vit B12, 4000 mcg per day by my Endo. The chemist has dispensed Cyanocominn which I understand is a synthetic Vit B preparation and I am led to believe not a good idea to take. Should I insist the chemist dispenses only natural
In addition to my daily Thyroxine dose of 100mcg I have been prescribed Vit B12, 4000 mcg per day by my Endo. The chemist has dispensed Cyanocominn which I understand is a synthetic Vit B preparation and I am led to believe not a good idea to take. Should I insist the chemist dispenses only natural
LONGEATON
in
Thyroid UK
26 days ago
GP wanting to report high liver blood test results to DVLA
Hi. This is my first post and I would be grateful of any advice or your experience in relation to this. My husband has been a heavy drinker (evenings and weekends) for a number of years. Blood tests in October showed high levels re health of his liver (not sure of all of the names) and subsequently
Hi. This is my first post and I would be grateful of any advice or your experience in relation to this. My husband has been a heavy drinker (evenings and weekends) for a number of years. Blood tests in October showed high levels re health of his liver (not sure of all of the names) and subsequently
OfftowalktheCamino
in
British Liver Trust
8 months ago
Weakness
Hello,I've had rheumatoid arthritis 28 years been on different drugs over years ,I have been methotrexate 25mg weekly for years folic acid I've been on rituximab every 6 months first course then 2 weeks later 2nd course for 4 year ,I'm starting to feel very weak I'm normally won't let it beat me ,I feel
Hello,I've had rheumatoid arthritis 28 years been on different drugs over years ,I have been methotrexate 25mg weekly for years folic acid I've been on rituximab every 6 months first course then 2 weeks later 2nd course for 4 year ,I'm starting to feel very weak I'm normally won't let it beat me ,I feel
Justlucy
in
NRAS
6 months ago
Blood tests MMA, B12
A conundrum about blood tests: I know that once substituting B12 blood levels are not reliable and that MMS should be tested instead. But if not substituting B12: do high B12 levels mean that there is no deficiency or should MMS and Homocysteine always be the preferred values? (My husband has blood
A conundrum about blood tests: I know that once substituting B12 blood levels are not reliable and that MMS should be tested instead. But if not substituting B12: do high B12 levels mean that there is no deficiency or should MMS and Homocysteine always be the preferred values? (My husband has blood
milupa
in
Thyroid UK
27 days ago
advice pls....
do you know if there is a list of UK doctors that are B12 experts? I have parietal cell antibodies but not IF antibodies so not diagnosed with pernicious anaemia. Bloods in Aug '23 showed B12 at 150 so was started in B12 injections (I had no symptoms of low b12 apart from slightly tired) Had loading
do you know if there is a list of UK doctors that are B12 experts? I have parietal cell antibodies but not IF antibodies so not diagnosed with pernicious anaemia. Bloods in Aug '23 showed B12 at 150 so was started in B12 injections (I had no symptoms of low b12 apart from slightly tired) Had loading
bollin
in
Pernicious Anaemia Society
27 days ago
Rheumy Nurse?
I am puzzled. This site has many references to apparent support teams. I am delighted if that is general. For myself the only contact with the NHS I have is my GP. It is alleged that there is a very overdue appointment with a consultant. Maybe I shall be able to elicit information about some kind
I am puzzled. This site has many references to apparent support teams. I am delighted if that is general. For myself the only contact with the NHS I have is my GP. It is alleged that there is a very overdue appointment with a consultant. Maybe I shall be able to elicit information about some kind
Colaba
in
NRAS
6 months ago
update on test results
hi all so the doctor rang me and told me to lower my thyroxine down to 150 mg and she said my iron levels were 10 so on the borderline, she didn’t give me any tablets for this so I don’t know if I’m doing the right thing but I’ve bought some ferogloblin capsules with folic acid vitamin b12 and iron thanks
hi all so the doctor rang me and told me to lower my thyroxine down to 150 mg and she said my iron levels were 10 so on the borderline, she didn’t give me any tablets for this so I don’t know if I’m doing the right thing but I’ve bought some ferogloblin capsules with folic acid vitamin b12 and iron thanks
Baileyleigh123
in
Thyroid UK
29 days ago
B12 def
I've been B12 deficient for decades. I ended up going back to school and finishing my PhD in both pharmacology and biochemistry and focused my research for 12 years on B12.
I've been B12 deficient for decades. I ended up going back to school and finishing my PhD in both pharmacology and biochemistry and focused my research for 12 years on B12.
B12phd
in
Pernicious Anaemia Society
30 days ago
Genes affecting B12
Hi all and in response to Litatamon B12life (don’t know how to highlight names to get their attention) During a discussion recently on B2 deficiency, I mentioned genes affecting B12 and was asked what they were So sorry for delayed response : Gene MTRR - rs id - rs1801394 effect allele G (Methylation
Hi all and in response to Litatamon B12life (don’t know how to highlight names to get their attention) During a discussion recently on B2 deficiency, I mentioned genes affecting B12 and was asked what they were So sorry for delayed response : Gene MTRR - rs id - rs1801394 effect allele G (Methylation
Bacca
in
Pernicious Anaemia Society
1 month ago
HRT Raises Rheumatoid Arthritis Risk …
I found this article last week about HRT and rheumatoid arthritis risk in my online magazine …. I know a lot of US use HRT and thought this article might be of interest. I don’t have the actual magazine its online subscription… sorry. This link might actually get you to this article! https://www.wddty.com
I found this article last week about HRT and rheumatoid arthritis risk in my online magazine …. I know a lot of US use HRT and thought this article might be of interest. I don’t have the actual magazine its online subscription… sorry. This link might actually get you to this article! https://www.wddty.com
Batty1
in
Thyroid UK
6 months ago
Low BP
I've used Amlodipine for long time to help Raynauds, recently BP has become quite low so have stopped Amlodipine. Has anyone used Naftidrofuryl as it has been suggested as doesn't lower BP.
I've used Amlodipine for long time to help Raynauds, recently BP has become quite low so have stopped Amlodipine. Has anyone used Naftidrofuryl as it has been suggested as doesn't lower BP.
Fishie1
in
Scleroderma & Raynaud's UK (SRUK)
5 months ago
thyroid results
Could someone please help me understand my blood results which I had done by Medichecks (home testing kit) I have had underactive thyroid for the past 25years The doctors are always changing the brands I take I hadn’t had my thyroid levels tested for nearly 5 years with my GP, it’s as if they’d
Could someone please help me understand my blood results which I had done by Medichecks (home testing kit) I have had underactive thyroid for the past 25years The doctors are always changing the brands I take I hadn’t had my thyroid levels tested for nearly 5 years with my GP, it’s as if they’d
Horsemadlindy21
in
Thyroid UK
6 months ago
Barry
Hi, stage 4 prostate cancer 9 months in on anti testerone injections degatelix psa level has risen from 77 to 323, what are my chances?
Hi, stage 4 prostate cancer 9 months in on anti testerone injections degatelix psa level has risen from 77 to 323, what are my chances?
littlemount
in
Advanced Prostate Cancer
8 months ago
advice re 0.02 reading
Hi everyone my first ever psa age 53 no symptoms 3.1 jan 2022 mri pri 3 hard prostate Gleason 3+3 no other scans mri did not detect the size of tumour l was told to go on active surveillance My brain said no ,choice given to me was remove prostate or brachytherapy l had operation in May 2022 all good
Hi everyone my first ever psa age 53 no symptoms 3.1 jan 2022 mri pri 3 hard prostate Gleason 3+3 no other scans mri did not detect the size of tumour l was told to go on active surveillance My brain said no ,choice given to me was remove prostate or brachytherapy l had operation in May 2022 all good
Ffghytrrg
in
Advanced Prostate Cancer
8 months ago
What were your first symptoms?
Over the last couple of months I've been getting pain in my fingers and toes, it happens several times a day but only lasts a minute or two at a time at the moment. I have autoimmune thyroid disease, and suspected autoimmune cause for my early menopause, and I'm acutely aware that autoimmune diseases
Over the last couple of months I've been getting pain in my fingers and toes, it happens several times a day but only lasts a minute or two at a time at the moment. I have autoimmune thyroid disease, and suspected autoimmune cause for my early menopause, and I'm acutely aware that autoimmune diseases
WitchingHour2point0
in
NRAS
6 months ago
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