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Carcinoembryonic antigen (CEA) test
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this might help
i’ve had scabies for the last month and a half, and I have done as much research as possible. Couldn’t find anything that was working for me today I took petroleum jelly, mixed it with tea tree oil, smothered my body in. It sat around in it for five hours, watching the scabies pour out of my body, wiping
i’ve had scabies for the last month and a half, and I have done as much research as possible. Couldn’t find anything that was working for me today I took petroleum jelly, mixed it with tea tree oil, smothered my body in. It sat around in it for five hours, watching the scabies pour out of my body, wiping
Tina2479
in
BASHH
1 month ago
What AI Says About Supplements and Off-Label Drug Use Regarding Prostate Cancer
Sure wish I had this tool over 2 years ago when I started reading up although you can't 100% trust the answers. The tools are getting smarter. I'm a software developer and have early access to Google's Gemini Pro 1.5 AI model that was relased Feb 15 2024 claiming to have better 'scores' than all the
Sure wish I had this tool over 2 years ago when I started reading up although you can't 100% trust the answers. The tools are getting smarter. I'm a software developer and have early access to Google's Gemini Pro 1.5 AI model that was relased Feb 15 2024 claiming to have better 'scores' than all the
jazj
in
Advanced Prostate Cancer
2 months ago
Mucinous ovarian cancer
I've recently had my 3 month review and blood
test
results. Thankfully my CA125 and
CEA
levels are normal. I'm obviously relieved as I've not been able to sleep thinking about it and worrying. I guess I'd like reassurance that it does get easier?
I've recently had my 3 month review and blood
test
results. Thankfully my CA125 and
CEA
levels are normal. I'm obviously relieved as I've not been able to sleep thinking about it and worrying. I guess I'd like reassurance that it does get easier?
Golden01
in
My Ovacome
2 months ago
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High-Dose Vitamin B1 / Thiamine and Fat Soluble Benfotiamine Form
I am reposting a reply to the Vitamin B1 thread as I noticed a search on HealthUnlocked for Benfotiamine doesn't list the thread for Vitamin B1 and the information I posted doesn't fit in one reply. I'm not giving medical advice but I know a lot of people here are open to trying things and watch if
I am reposting a reply to the Vitamin B1 thread as I noticed a search on HealthUnlocked for Benfotiamine doesn't list the thread for Vitamin B1 and the information I posted doesn't fit in one reply. I'm not giving medical advice but I know a lot of people here are open to trying things and watch if
jazj
in
Advanced Prostate Cancer
3 months ago
Demodex Blepharitis treatments?
Hello, all. Glaucoma diagnosed late 2019. Initially drops tolerated ok think Latanoprost plus other.After a while developed bad red eyes, itching. Tried various drops since including preservative free, had both cataracts done. Tablets Azetazoloimide? Worked well, not able stay on them! Stopped taking
Hello, all. Glaucoma diagnosed late 2019. Initially drops tolerated ok think Latanoprost plus other.After a while developed bad red eyes, itching. Tried various drops since including preservative free, had both cataracts done. Tablets Azetazoloimide? Worked well, not able stay on them! Stopped taking
TVTech
in
Glaucoma UK
3 months ago
From a Gleason 9 to a clean CT scan in 18 mos.
18 mos ago, my husband was told by his dr. that he "most likely had two or three good years left." (WHY do they say stupid things like that?) I think that a lot of people believe whatever the dr. says and subconsciously program themselves accordingly. I, on the other hand, thought to myself, "We'll
18 mos ago, my husband was told by his dr. that he "most likely had two or three good years left." (WHY do they say stupid things like that?) I think that a lot of people believe whatever the dr. says and subconsciously program themselves accordingly. I, on the other hand, thought to myself, "We'll
jtango
in
Advanced Prostate Cancer
6 months ago
Vitamins/supplements for cll?
I found out AFTER I was diagnosed with CLL that low vitamin D is a risk factor for getting CLL. I have had chronically low vitamin D even though I worked outside for half my working life. I was haphazard in supplementing the past 30 years. With recent research, I'm seeing all kinds of supposedly helpful
I found out AFTER I was diagnosed with CLL that low vitamin D is a risk factor for getting CLL. I have had chronically low vitamin D even though I worked outside for half my working life. I was haphazard in supplementing the past 30 years. With recent research, I'm seeing all kinds of supposedly helpful
Vivikaye1
in
CLL Support
6 months ago
CA 27.29 Blood test
My new oncologist wants to add a new tumor marker
test
to my regular tests for CA15 and
CEA
. I know these guys all have widely varying ideas on which ones - if any - mean anything. So just looking to see if you all have any experience with this.
My new oncologist wants to add a new tumor marker
test
to my regular tests for CA15 and
CEA
. I know these guys all have widely varying ideas on which ones - if any - mean anything. So just looking to see if you all have any experience with this.
Iwasborntodothis
in
SHARE Metastatic Breast Cancer
2 months ago
Switch to Mucuna
Apologies if this has been asked and answered earlier. I am looking for a guide to switch from C/L to Green tea/Mucuna. Is there a method to calculate green tea against equivalent carbidopa doses? Is brewed green tea better or green tea extract capsule? Is there any interaction between green tea and
Apologies if this has been asked and answered earlier. I am looking for a guide to switch from C/L to Green tea/Mucuna. Is there a method to calculate green tea against equivalent carbidopa doses? Is brewed green tea better or green tea extract capsule? Is there any interaction between green tea and
JayPwP
in
Cure Parkinson's
10 months ago
Do your oncologists ask for the CEA test with the CA15-3 or CA27.29
when I have my CA15-3 blood
test
, my oncologist also asks that I get the
CEA
test
as well. But he keeps saying that the
CEA
is non specific. Do any of you ladies have this done regularly?
when I have my CA15-3 blood
test
, my oncologist also asks that I get the
CEA
test
as well. But he keeps saying that the
CEA
is non specific. Do any of you ladies have this done regularly?
MyMiracle13
in
SHARE Metastatic Breast Cancer
2 years ago
DX 5 years on Dec 26th. What I’ve learned about my PD. Please Read! It might be helpful.
PD is very common in my family. My dad and his dad had it. I have almost no hope they will ever cure it because it’s so complex. Here is what caused my Parkinson’s. (IMO) 1.Genetics. This is something you cannot change. I know my genes have issues with clearing out toxins? PD is a man made disease
PD is very common in my family. My dad and his dad had it. I have almost no hope they will ever cure it because it’s so complex. Here is what caused my Parkinson’s. (IMO) 1.Genetics. This is something you cannot change. I know my genes have issues with clearing out toxins? PD is a man made disease
38yroldmale
in
Cure Parkinson's
4 months ago
First six-month blood test, and my lymphocytes have gone down!
I’m soon to be 55. I was diagnosed in the UK with MBL this summer. My lymphocytes were at six with over 50% of them monoclonal cells. I’ve just had my six-month check. I’ve come down to 4.8. I know that these numbers can move around quite a lot, but for now I’m really happy with the trend. I did change
I’m soon to be 55. I was diagnosed in the UK with MBL this summer. My lymphocytes were at six with over 50% of them monoclonal cells. I’ve just had my six-month check. I’ve come down to 4.8. I know that these numbers can move around quite a lot, but for now I’m really happy with the trend. I did change
Jazzandblues
in
CLL Support
4 months ago
Dry eyes and mouth
Is sea buckthorn oil capsules good for sjogrens syndrome? I had this diagnosis yrs ago and I know there is a correlation between sjogrens and hashimotos which I also have. Tried lots of eye lubricants (Prescriotion and OTC ) and oral sprays over the years but nothing has helped. Think I may have heard
Is sea buckthorn oil capsules good for sjogrens syndrome? I had this diagnosis yrs ago and I know there is a correlation between sjogrens and hashimotos which I also have. Tried lots of eye lubricants (Prescriotion and OTC ) and oral sprays over the years but nothing has helped. Think I may have heard
Hollybushroad
in
Thyroid UK
10 months ago
I got impetigo and I’m due to get my Covid booster
hi all, hope you are all enjoying the nice weather although from indoors. I was going to the gym up to last week and since Tuesday I got impetigo in my face. At first I thought it was a cold sore but I don’t usually have cold sores and this was itchy and had a runny liquid so I went to the pharmacy and
hi all, hope you are all enjoying the nice weather although from indoors. I was going to the gym up to last week and since Tuesday I got impetigo in my face. At first I thought it was a cold sore but I don’t usually have cold sores and this was itchy and had a runny liquid so I went to the pharmacy and
EG74
in
LUPUS UK
10 months ago
Advice please for next Roseway appt
What size T4 capsules should I ask for next? I currently take 125mcg split as 2 x 50 and 1 x 25. I'm taking Roseway's compounded T4 capsules so they can't easily be split. I had to test this week as I need my appointment next week in order not to run out, but I only completed my transition from NDT
What size T4 capsules should I ask for next? I currently take 125mcg split as 2 x 50 and 1 x 25. I'm taking Roseway's compounded T4 capsules so they can't easily be split. I had to test this week as I need my appointment next week in order not to run out, but I only completed my transition from NDT
FoggyThinker
in
Thyroid UK
1 hour ago
Rheumatologist advices no reduction of prednisolone while adrenal glands not working and has issued emergency hydrocortisone kit
I've had PMR since October 2020 and managed to get down to 2.5mg of prednisolone in February 2023. But after a flare, I had to raise it to 5mg and have been pain-free since then. I started on methotrexate weekly injections (15mg) in December 2023, with the hope of being able to reduce the prednisolone
I've had PMR since October 2020 and managed to get down to 2.5mg of prednisolone in February 2023. But after a flare, I had to raise it to 5mg and have been pain-free since then. I started on methotrexate weekly injections (15mg) in December 2023, with the hope of being able to reduce the prednisolone
harpsichor
in
PMRGCAuk
7 hours ago
Cortisol issues
I'm fortunate in having a good GP who is very concerned about my total exhaustion and inability to cope with everyday life. She wrote to my rheumy who authorised a 9am cortisol test. It came back as 104 and he has arranged a short synacthen test in two months time. I've asked the rheumatology dept for
I'm fortunate in having a good GP who is very concerned about my total exhaustion and inability to cope with everyday life. She wrote to my rheumy who authorised a 9am cortisol test. It came back as 104 and he has arranged a short synacthen test in two months time. I've asked the rheumatology dept for
Sammo47
in
PMRGCAuk
12 hours ago
Other blood results
I now have more results Serum folate 14.3 (3.1-17.5) Ferritin 138 (13-150) Iron 14 (5-28) B12 280 (200-940) Since they are in the range ‘everything is normal’! The coeliac one was clear so I can now try gluten free for 3 months to see if it makes any changes. But I am still tired, muscle aches
I now have more results Serum folate 14.3 (3.1-17.5) Ferritin 138 (13-150) Iron 14 (5-28) B12 280 (200-940) Since they are in the range ‘everything is normal’! The coeliac one was clear so I can now try gluten free for 3 months to see if it makes any changes. But I am still tired, muscle aches
Purple450
in
Thyroid UK
23 hours ago
TEVA 100mcg Thyroxine
I had taken another brand for many years and have now been switched to TEVA. This happened a short while ago and since then I feel much more tired with aching joints. Is this coincidence? Overall my dose has been reduced from 100/day to 100 Mon-Fri and 75 Sat, Sun. This is addition to T3 12.5 mcg
I had taken another brand for many years and have now been switched to TEVA. This happened a short while ago and since then I feel much more tired with aching joints. Is this coincidence? Overall my dose has been reduced from 100/day to 100 Mon-Fri and 75 Sat, Sun. This is addition to T3 12.5 mcg
RichardEva
in
Thyroid UK
1 day ago
T3 tablets
Where can I buy Tiromel at a reasonable price or other T3 that isn't very expensive?Thanks
Where can I buy Tiromel at a reasonable price or other T3 that isn't very expensive?Thanks
SALAD8
in
Thyroid UK
1 day ago
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