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problem with Thriva - IT
I ordered some blood tests last Thursday. They took my card payment but the completed final screen never loaded. I didn’t receive an order confirmation email. I haven’t received the kit. I emailed them but no reply. I just emailed them again and got an auto bounce back ( correction - auto reply ) .
I ordered some blood tests last Thursday. They took my card payment but the completed final screen never loaded. I didn’t receive an order confirmation email. I haven’t received the kit. I emailed them but no reply. I just emailed them again and got an auto bounce back ( correction - auto reply ) .
Applethorpe
in
Thyroid UK
7 months ago
Frozen DE treatment cycle different to FET with OE
Hello All, I think I’m missing something obvious but can anyone explain why a frozen DE treatment cycle plans the transfer for day 22-24 while both my FETs have been transferred on day 17 ish? I’m anxious because after a mmc with my last FET, I hope this was a sign of receptivity at 17 day mark and
Hello All, I think I’m missing something obvious but can anyone explain why a frozen DE treatment cycle plans the transfer for day 22-24 while both my FETs have been transferred on day 17 ish? I’m anxious because after a mmc with my last FET, I hope this was a sign of receptivity at 17 day mark and
Kitkat10
in
Fertility Network UK
7 months ago
Life After Rituximab - Is that it?
So that time has come when I am having my last Rituximab infusion on the 22nd November, it’s been 3 years on the treatment and my Consultant has told me that’s the max. My ANCA marker is low but what happens next? I have a Consultation with my Consultant on the 20th October and of course I will ask her
So that time has come when I am having my last Rituximab infusion on the 22nd November, it’s been 3 years on the treatment and my Consultant has told me that’s the max. My ANCA marker is low but what happens next? I have a Consultation with my Consultant on the 20th October and of course I will ask her
Investigator1
in
Vasculitis UK
7 months ago
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Blood tests while on NDT
Hello, When doing blood tests while on NDT, when is the best time to do them? And when should the last dose of NDT should be the previous day? For reference, I take half a dose at 4 AM and half at 12 PM. I have the blood test scheduled at my GP at 8:15 AM.
Hello, When doing blood tests while on NDT, when is the best time to do them? And when should the last dose of NDT should be the previous day? For reference, I take half a dose at 4 AM and half at 12 PM. I have the blood test scheduled at my GP at 8:15 AM.
Alex_p
in
Thyroid UK
7 months ago
lupus ?
I've been unwell for 5 yrs on and off ..whole body rash,widespread joint pain ,low grade fevers ,photosensitivity ,hair loss and generally feeling rubbish and fatigued and chronic autoimmune urticaria and most recently I am unable to stand for long periods of time as I have horrendous pain in both my
I've been unwell for 5 yrs on and off ..whole body rash,widespread joint pain ,low grade fevers ,photosensitivity ,hair loss and generally feeling rubbish and fatigued and chronic autoimmune urticaria and most recently I am unable to stand for long periods of time as I have horrendous pain in both my
shell9518
in
LUPUS UK
7 months ago
24,000 hospital letters lost due to NHS computer glitch
I am posting this not to start discussion about the health service but in case we have members who are directly affected by these issues. This article should help to inform why information has not flowed. And prompt anyone to check whether they are affected, For that reason, I shall close it to replying
I am posting this not to start discussion about the health service but in case we have members who are directly affected by these issues. This article should help to inform why information has not flowed. And prompt anyone to check whether they are affected, For that reason, I shall close it to replying
helvella
Thyroid UK
in
Thyroid UK
7 months ago
Fragile Skin and cuts, increased CRP and Chest Infection and reducing pred.
Hi you lovely people it doesnt seem that long since my last post asking for your advice regarding my 86 year old mums struggles with achilles tendonitis before my nieces wedding. As usual your advice was invaluable then and my mum managed to have a lovely day at the wedding and she looked beautiful.However
Hi you lovely people it doesnt seem that long since my last post asking for your advice regarding my 86 year old mums struggles with achilles tendonitis before my nieces wedding. As usual your advice was invaluable then and my mum managed to have a lovely day at the wedding and she looked beautiful.However
Buchanan16
in
PMRGCAuk
7 months ago
Being anxious about Hypothyroidism
In about May 2023 I was sent as a matter of urgency to a doctor (I had just changed surgery due to moving, but I don't have much of a history of bothering with doctors anyway) because I had a pre-op medical (bloods, weight, heart etc) and a nurse discovered a thyroid problem. So I went to the doctors
In about May 2023 I was sent as a matter of urgency to a doctor (I had just changed surgery due to moving, but I don't have much of a history of bothering with doctors anyway) because I had a pre-op medical (bloods, weight, heart etc) and a nurse discovered a thyroid problem. So I went to the doctors
Dakota1234
in
Thyroid UK
7 months ago
Signatera Blood Test for EC
Is anybody using the Signatera blood test to detect cancer recurrence? I do not think that it has been approved by the FDA for endometrial cancer, but I've heard that some people pay out of pocket for it and that it can pick up the presence of circulating cancer cells before a CT scan will show anything
Is anybody using the Signatera blood test to detect cancer recurrence? I do not think that it has been approved by the FDA for endometrial cancer, but I've heard that some people pay out of pocket for it and that it can pick up the presence of circulating cancer cells before a CT scan will show anything
FierceFriend
in
SHARE Uterine Cancer Support
7 months ago
Support needed please
Hi all, I took the plunge today and called the doctor to get more details on assisted conception. We have been trying for around 4 years with no luck. We both had test done last year (Sept-Dec) including blood tests, swabs, external and internal ultrasound and sample tests for my husband. We were told
Hi all, I took the plunge today and called the doctor to get more details on assisted conception. We have been trying for around 4 years with no luck. We both had test done last year (Sept-Dec) including blood tests, swabs, external and internal ultrasound and sample tests for my husband. We were told
PeachesGirl
in
Fertility Network UK
7 months ago
worried
Hello Im new to this group, I was diagnosed with NAFLD in March 2023 after an appointment for weight loss it seems it showed up in a blood test and a scan. I was then sent for a fibro scan. I had this and the technician said my ribs were fused and she could only get 5 readings instead of 10 to get a
Hello Im new to this group, I was diagnosed with NAFLD in March 2023 after an appointment for weight loss it seems it showed up in a blood test and a scan. I was then sent for a fibro scan. I had this and the technician said my ribs were fused and she could only get 5 readings instead of 10 to get a
France19
in
British Liver Trust
7 months ago
Not obvious query
This question applies to Hashimottos and it may be a strange one but I can't find the answer anywhere on the Internet. For those that have Hashimottos does it eventually get to the stage where our antibodies completely destroy the thyroid and then we are left on a stable dose of levothyroxine without
This question applies to Hashimottos and it may be a strange one but I can't find the answer anywhere on the Internet. For those that have Hashimottos does it eventually get to the stage where our antibodies completely destroy the thyroid and then we are left on a stable dose of levothyroxine without
mle121
in
Thyroid UK
7 months ago
Glum. Grim. Grumpy.
Had my levothyroxine increased to 75 last Thursday. Crikey on a bikey…feel terrible. All the symptoms that I had before I started levo went away for a while after a few weeks on the 50mcg and then came back so last week the Gp agreed an increase. This weekend it all seems to have ramped up again. Lay
Had my levothyroxine increased to 75 last Thursday. Crikey on a bikey…feel terrible. All the symptoms that I had before I started levo went away for a while after a few weeks on the 50mcg and then came back so last week the Gp agreed an increase. This weekend it all seems to have ramped up again. Lay
JoJoloveschocolate
in
Thyroid UK
7 months ago
Great doctor!
I want to share my experience with my lovely new doctor! I thought from my conversation that he had PA like me. It turns out itis a very rare condition that took years of frustration like us to be diagnosed and has left him with intense chronic pain and debilitating exhaustion He can only work 3days
I want to share my experience with my lovely new doctor! I thought from my conversation that he had PA like me. It turns out itis a very rare condition that took years of frustration like us to be diagnosed and has left him with intense chronic pain and debilitating exhaustion He can only work 3days
brenanddave
in
Pernicious Anaemia Society
8 months ago
blood test showed high ALT levels
Hi so recently had a blood test done everything was fine apart from my liver my ALT level 18 months ago was 26 now it’s 106 🤷♀️. My doctor has booked me in for an abdominal scan so waiting on that. Nothing has changed for this to warrant this reading. I suffer from IBS and I am currently pre menopausal
Hi so recently had a blood test done everything was fine apart from my liver my ALT level 18 months ago was 26 now it’s 106 🤷♀️. My doctor has booked me in for an abdominal scan so waiting on that. Nothing has changed for this to warrant this reading. I suffer from IBS and I am currently pre menopausal
Junkjournal1
in
IBS Network
8 months ago
Prednisone to Hydrocortisone
My last visit to my rheumatologist she recommended I see an endocrinologist because my most recent Dexa scan (2022) hadn’t improved from my last one (2020). My Dexa scans say osteopenia but my rheumatologist looks at the reports and there’s some other formula that brings me into osteoporosis. So she
My last visit to my rheumatologist she recommended I see an endocrinologist because my most recent Dexa scan (2022) hadn’t improved from my last one (2020). My Dexa scans say osteopenia but my rheumatologist looks at the reports and there’s some other formula that brings me into osteoporosis. So she
1951grumpa
in
PMRGCAuk
8 months ago
Supplements before Diagnostic Blood Tests - Newbie Question
Hello I’ve had unexplained fatigue and neurological symptoms for 10+ years. I recently found out about PA. The symptoms fit my profile and when I mentioned PA to my mum she remembered that two of my great aunts had it. I have Hashimoto’s and psoriasis. So it looks like PA is worth investigating. I
Hello I’ve had unexplained fatigue and neurological symptoms for 10+ years. I recently found out about PA. The symptoms fit my profile and when I mentioned PA to my mum she remembered that two of my great aunts had it. I have Hashimoto’s and psoriasis. So it looks like PA is worth investigating. I
Harpee
in
Pernicious Anaemia Society
8 months ago
stopping bisopromol
Hi All, hope you are keeping well. In the last 18 months I’ve paid privately to see the consultant who put the stent inside of me. It started with paying for an echo cardio gram and also a fitness test because I put it down to the meds I was on, but that general feeling of dog****. Fatigued.
Hi All, hope you are keeping well. In the last 18 months I’ve paid privately to see the consultant who put the stent inside of me. It started with paying for an echo cardio gram and also a fitness test because I put it down to the meds I was on, but that general feeling of dog****. Fatigued.
SteveWX
in
British Heart Foundation
8 months ago
How often should inject?
Background: Diagnosed 9 years ago with ME and fibro (b12 not tested). Been bedbound since but was slowly getting a bit better, then got covid and I never really recovered. Also have no working pituitary since birth. Asked for doctor to do blood tests and came back with b12 at 194. Was told to take supplements
Background: Diagnosed 9 years ago with ME and fibro (b12 not tested). Been bedbound since but was slowly getting a bit better, then got covid and I never really recovered. Also have no working pituitary since birth. Asked for doctor to do blood tests and came back with b12 at 194. Was told to take supplements
Pepperpots302
in
Pernicious Anaemia Society
8 months ago
Last hope
Hi,14 months on from pace and ablate and I am still struggling with chest discomfort weakness, breathlessness, exhaustion on exertion which also causes that I can only describe as intense pumping of the heart, not fast but hard beats which causes me to feel week in the lower half and dizzy, lightheaded
Hi,14 months on from pace and ablate and I am still struggling with chest discomfort weakness, breathlessness, exhaustion on exertion which also causes that I can only describe as intense pumping of the heart, not fast but hard beats which causes me to feel week in the lower half and dizzy, lightheaded
Nomis21
in
AF Association
8 months ago
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