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Biotin
Hi please can you tell me how much biotin would affect blood test results. I am waiting for a doctors appointment , they have told me it will be between 2 and 4 weeks, but could be sooner. I am currently taking B complex supplement which contains biotin. I know the guideline is don't take for 7 days.
Hi please can you tell me how much biotin would affect blood test results. I am waiting for a doctors appointment , they have told me it will be between 2 and 4 weeks, but could be sooner. I am currently taking B complex supplement which contains biotin. I know the guideline is don't take for 7 days.
Shellian
in
Thyroid UK
6 months ago
life after heart attack
I had a stemi attack 5 weeks ago. 4 stents fitted three weeks ago. I thought I had indigestion /fluso never went doctors for few days after gp blood test I was sent an ambulance to my home a few hours later. At 50 years old it turned my world upside down. I am thankful to all the amazing staff for ultimately
I had a stemi attack 5 weeks ago. 4 stents fitted three weeks ago. I thought I had indigestion /fluso never went doctors for few days after gp blood test I was sent an ambulance to my home a few hours later. At 50 years old it turned my world upside down. I am thankful to all the amazing staff for ultimately
4stentstemi
in
British Heart Foundation
6 months ago
Week 2 - Done
Since I'm spreading this week out to get back to Monday/Wednesday/Friday running, I did W2R3 today, it seems strange leaving so much time between the runs but I'll be back to the preferred routine next week. A nice HR controlled joffle, most time spent in the aerobic zone, rising to threshold during
Since I'm spreading this week out to get back to Monday/Wednesday/Friday running, I did W2R3 today, it seems strange leaving so much time between the runs but I'll be back to the preferred routine next week. A nice HR controlled joffle, most time spent in the aerobic zone, rising to threshold during
LeeU
Graduate
in
Couch to 5K
1 year ago
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By how should I increase my prednisone?
Hi All,I have had PMR since 2011 when diagnosed. I had got down to 5mg of pred and was on this dosage for many years until I had a massive flare at the beginning of 2023 and I increased my dosage, then gradually came down to 8 and 3/4mg. I am a 72 year old fit male. I have been going to my physiotherapist
Hi All,I have had PMR since 2011 when diagnosed. I had got down to 5mg of pred and was on this dosage for many years until I had a massive flare at the beginning of 2023 and I increased my dosage, then gradually came down to 8 and 3/4mg. I am a 72 year old fit male. I have been going to my physiotherapist
Buenavista
in
PMRGCAuk
6 months ago
Alcohol home detox
hi everyone my daughter is an alcoholic and has many health issues related to her drinking. She is waiting to do a home detox which is being arranged through turning point. (She doesn’t want to go to a clinic) She was previously given a date for this but was told by the doctor at turning point that
hi everyone my daughter is an alcoholic and has many health issues related to her drinking. She is waiting to do a home detox which is being arranged through turning point. (She doesn’t want to go to a clinic) She was previously given a date for this but was told by the doctor at turning point that
Bellabinx
in
British Liver Trust
6 months ago
Hashimoto diagnosis
I have just found out the I have Hashimotos Disease and am going down the rabbit warren of Google trying to research what it is. How to live with it? What I can do to help myself? And generally get my head around the fact I have it. Hopefully I might get some pointers on here of good places to look and
I have just found out the I have Hashimotos Disease and am going down the rabbit warren of Google trying to research what it is. How to live with it? What I can do to help myself? And generally get my head around the fact I have it. Hopefully I might get some pointers on here of good places to look and
Crazylegs16
in
Thyroid UK
6 months ago
Newly diagnosed metastatic PC treatment options
Hi, I'm 68 years old. Here are the key points in my story so far: In July 2023 a blood test showed a PSA value of 45. On September 26 2023, prostate MRI showed a dominant tumor in the prostate with extension into the right seminal vesicle. Also the fat plane between the rectum and prostate is lost
Hi, I'm 68 years old. Here are the key points in my story so far: In July 2023 a blood test showed a PSA value of 45. On September 26 2023, prostate MRI showed a dominant tumor in the prostate with extension into the right seminal vesicle. Also the fat plane between the rectum and prostate is lost
ShorePine
in
Advanced Prostate Cancer
6 months ago
Worried
hi, I have joined this group for some advice please. I was 65 in August and a few weeks later started with painful hips, eye aches and occasional sharp fleeting pains in my temple area. They aren’t constant and some days very few. I was due to go on holiday abroad so GP did some blood tests. ESR was
hi, I have joined this group for some advice please. I was 65 in August and a few weeks later started with painful hips, eye aches and occasional sharp fleeting pains in my temple area. They aren’t constant and some days very few. I was due to go on holiday abroad so GP did some blood tests. ESR was
Pennypip
in
PMRGCAuk
6 months ago
Worried
hi I joined this group over a year ago I often read some of the posts and find them informative. I’m a bit of a technophobe and this is my first time posting for advice. I was 65 in August and a few weeks later started having painful hips, eye aches and occasional sharp fleeting pains in my temples
hi I joined this group over a year ago I often read some of the posts and find them informative. I’m a bit of a technophobe and this is my first time posting for advice. I was 65 in August and a few weeks later started having painful hips, eye aches and occasional sharp fleeting pains in my temples
Pennypip
in
LUPUS UK
6 months ago
high alp. Very worried
hello. I posted before but I need to clarify a few points. I had blood test recently which came back Alp 177 and Alt 50. Everything else ok. I do not currently have a diagnosis of liver disease…..well not yet! I am not on any medication. Over the years I have drunk too much white wine but never
hello. I posted before but I need to clarify a few points. I had blood test recently which came back Alp 177 and Alt 50. Everything else ok. I do not currently have a diagnosis of liver disease…..well not yet! I am not on any medication. Over the years I have drunk too much white wine but never
Watersk
in
British Liver Trust
6 months ago
Blood test results - best practice
I have had rheumatoid disease for about nine months now and it has been really difficult to get access to my blood test results. The hospital provide labels, the tests are done at my surgery and the results are sent to the hospital. The overworked team there are reluctant to share the results and my
I have had rheumatoid disease for about nine months now and it has been really difficult to get access to my blood test results. The hospital provide labels, the tests are done at my surgery and the results are sent to the hospital. The overworked team there are reluctant to share the results and my
spartacus101
in
NRAS
6 months ago
review appointment post failed transfer
I’ve requested a review apt. with my clinic following my failed implantation and period at 6dpt. I’m assuming this is a progesterone problem, in that my period should have held off for a lot longer. Without sounding silly…because this is a medicated cycle, is it completely dependent upon what level
I’ve requested a review apt. with my clinic following my failed implantation and period at 6dpt. I’m assuming this is a progesterone problem, in that my period should have held off for a lot longer. Without sounding silly…because this is a medicated cycle, is it completely dependent upon what level
CJohns
in
Fertility Network UK
6 months ago
constant abnormal blood results on Methotrexate
bloods have been abnormal pretty much every month for over a year now. Been on methotrexate 20mg since 2019 to treat mixed connective tissue disease. Symptoms have been pretty stable for nearly 3 years. Bloods however have shown low white blood cell count e see knots every blood test. Consultant/ nurse
bloods have been abnormal pretty much every month for over a year now. Been on methotrexate 20mg since 2019 to treat mixed connective tissue disease. Symptoms have been pretty stable for nearly 3 years. Bloods however have shown low white blood cell count e see knots every blood test. Consultant/ nurse
Melarky
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
Has anybody had any experience with an endoscopy?
Following a high fibroscan score I was referred to a liver consultant who wanted me to have another fibroscan last November (which was even higher) and blood tests which were done in March. To date I've heard nothing. Along side this I was also referred for gall bladderproblems. Saw the consultant
Following a high fibroscan score I was referred to a liver consultant who wanted me to have another fibroscan last November (which was even higher) and blood tests which were done in March. To date I've heard nothing. Along side this I was also referred for gall bladderproblems. Saw the consultant
Wordesley
in
British Liver Trust
6 months ago
To fast or not to fast?
Hi all, This may seem a bit silly but I don't ever remember being told to fast before blood tests (I am on MTX so for liver function, the usual...) when I lived in London. Living in Spain now where there's a blanket rule, fast before all blood tests. Can anyone tell me if it's usual to fast before
Hi all, This may seem a bit silly but I don't ever remember being told to fast before blood tests (I am on MTX so for liver function, the usual...) when I lived in London. Living in Spain now where there's a blanket rule, fast before all blood tests. Can anyone tell me if it's usual to fast before
Manzana1
in
NRAS
6 months ago
hashimotos and cortisol testing
Hi there because of the fatigue I am experiencing, I am thinking of having some tests done to see if my cortisol is ok. I am aware of the short synachten test, the straight forwards blood test for cortisol or the 4x a day saliva test. Not really sure where to start or if this will be useful to my healing
Hi there because of the fatigue I am experiencing, I am thinking of having some tests done to see if my cortisol is ok. I am aware of the short synachten test, the straight forwards blood test for cortisol or the 4x a day saliva test. Not really sure where to start or if this will be useful to my healing
Sammy333
in
Thyroid UK
6 months ago
new blood tests
Hct is lower again to 37 and Hgb 11.5, iron panel still anemic. New Blood Test. Anion Gap. Normal range per lab. 6-22 My test result was 3 Anyone have any insight? thank you
Hct is lower again to 37 and Hgb 11.5, iron panel still anemic. New Blood Test. Anion Gap. Normal range per lab. 6-22 My test result was 3 Anyone have any insight? thank you
Pickleball11
in
MPN Voice
6 months ago
Pulsatile tinnitus links to Folate B9 and cholesterol
I have Pulsatile Tinnitus. I’ve just had blood test results… along with my folate B9 levels (having been very low when I first developed PT) I also have high cholesterol… LDL (bad cholesterol) is slightly high at 3.6 (should be below 3) Serum cholesterol is 5.4 (should be below 5) My overall ratio
I have Pulsatile Tinnitus. I’ve just had blood test results… along with my folate B9 levels (having been very low when I first developed PT) I also have high cholesterol… LDL (bad cholesterol) is slightly high at 3.6 (should be below 3) Serum cholesterol is 5.4 (should be below 5) My overall ratio
PTNewbie
in
Tinnitus UK
6 months ago
first lap - nothing found. Please help.
Hi, I’m new here (or I’ve been acting like a shadow for months, reading your stories & experiences and feeling a sense of support from you all without reaching out, so firstly thank you) I have had ongoing pelvic pain since 2021. Continuously. It started as a niggle in my right ovary. I noticed it
Hi, I’m new here (or I’ve been acting like a shadow for months, reading your stories & experiences and feeling a sense of support from you all without reaching out, so firstly thank you) I have had ongoing pelvic pain since 2021. Continuously. It started as a niggle in my right ovary. I noticed it
GraceElli
in
Endometriosis UK
6 months ago
Pneumonia vaccination
Hi all. I have recently returned to Spain for the foreseeable future and managed to get my covid vaccination shortly after my arrival a few weeks ago. I had my flu vaccination in the UK just before we came out. I have to say that I have responded well to both vaccinations with no adverse side effects
Hi all. I have recently returned to Spain for the foreseeable future and managed to get my covid vaccination shortly after my arrival a few weeks ago. I had my flu vaccination in the UK just before we came out. I have to say that I have responded well to both vaccinations with no adverse side effects
Elispeth
in
PMRGCAuk
6 months ago
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