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Given Private Diagnosis But Antibody Test Is Negative? A Little Confused.
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
B12again
in
Pernicious Anaemia Society
1 month ago
Here's the tee shirt I'd like to see!
Multiple Sclerosis - "It's the stuff God hits your ass with when he doesn't want to kill ya -- just slow ya down." Richard Pyror, 1993, [i]Entertainment Weekly[/i]
Multiple Sclerosis - "It's the stuff God hits your ass with when he doesn't want to kill ya -- just slow ya down." Richard Pyror, 1993, [i]Entertainment Weekly[/i]
goatgal
in
My MSAA Community
1 month ago
Given Private Diagnosis But Antibody Test Is Negative?
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
I recently had a private diagnosis of Autoimmune Thyroiditis. This was given in the context of seeking a diagnosis of my B12 deficiency which was said to be linked with the above, Pernicious Anaemia, antibodies attacking thyroid and gastric parietal cells. I have been on levothyroxin for 15yrs. He based
B12again
in
Thyroid UK
1 month ago
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Treatment
My dears, after RP (Gleason 7, 4+3, infected 3 lymph nodes) and lymphadetectomy, radiation and hormone therapy for 39 months, my oncologist took me off hormone therapy with the recommendation of PSA control every 3 months. The last three PSA readings (every three months) were 0.01 / 0.00 / 0.00, I expect
My dears, after RP (Gleason 7, 4+3, infected 3 lymph nodes) and lymphadetectomy, radiation and hormone therapy for 39 months, my oncologist took me off hormone therapy with the recommendation of PSA control every 3 months. The last three PSA readings (every three months) were 0.01 / 0.00 / 0.00, I expect
adam1967adam
in
Advanced Prostate Cancer
6 months ago
Ivermectin may help with cancer treatments
Studies of various chronic myeloid leukemia cell lines show that ivermectin kills these lines by inducing mitochondrial dysfunction and the production of free radicals. In mice with leukemia, ivermectin increases the influx of chloride ions in the cells, promoting cell death. When ivermectin is combined
Studies of various chronic myeloid leukemia cell lines show that ivermectin kills these lines by inducing mitochondrial dysfunction and the production of free radicals. In mice with leukemia, ivermectin increases the influx of chloride ions in the cells, promoting cell death. When ivermectin is combined
craterlake
in
CLL Support
6 months ago
xtandi beginning to fail?
Seven months ago my PSA was 0.06. Three months ago PSA at my URO’s office was 0.11. I asked him if xtandi was beginning to fail me, he would not give me a answer. March 11th PSA at my MO’s office PSA was < 0.1. MO was happy with that number. I get checked again the 25th of this month at my URO. I
Seven months ago my PSA was 0.06. Three months ago PSA at my URO’s office was 0.11. I asked him if xtandi was beginning to fail me, he would not give me a answer. March 11th PSA at my MO’s office PSA was < 0.1. MO was happy with that number. I get checked again the 25th of this month at my URO. I
Echotango51
in
Advanced Prostate Cancer
6 months ago
documentary one in 37 by Cure Parkinson’s NZ
https://www.cureparkinsonsnz.org.nz/one-in-37-documentary/ ”Our full-length, 60-min documentary tells the personal stories of five individuals living with Parkinson’s disease and highlights the New Zealand research effort to develop therapies that can stop or slow disease progression. It also breaks
https://www.cureparkinsonsnz.org.nz/one-in-37-documentary/ ”Our full-length, 60-min documentary tells the personal stories of five individuals living with Parkinson’s disease and highlights the New Zealand research effort to develop therapies that can stop or slow disease progression. It also breaks
LAJ12345
in
Cure Parkinson's
6 months ago
Using regain with under active thyroid.
Hi everybody. I used regain years ago before I was diagnosed with underactive thyroid, I must have been loosing my hair due to my thyroid. The side effects were awful, I would wake up with heart palpitations in the middle of the night. I'm just wondering now that my thyroid is functioning better with
Hi everybody. I used regain years ago before I was diagnosed with underactive thyroid, I must have been loosing my hair due to my thyroid. The side effects were awful, I would wake up with heart palpitations in the middle of the night. I'm just wondering now that my thyroid is functioning better with
MrTHG
in
Thyroid UK
1 month ago
PSA, total
Hello. I know this forum is about advanced prostate cancer. I’m really hoping I’m not there yet. I had a RP June 2023 I just got the results from my forth PSA test the first three were a post prostatectomy PSA test and all three were 0.02 this last one was a PSA, total. That’s what the Urologist wanted
Hello. I know this forum is about advanced prostate cancer. I’m really hoping I’m not there yet. I had a RP June 2023 I just got the results from my forth PSA test the first three were a post prostatectomy PSA test and all three were 0.02 this last one was a PSA, total. That’s what the Urologist wanted
Elkguide
in
Advanced Prostate Cancer
6 months ago
Still fighting for a diagnosis B12, PA
Due to my ongoing failing health I've had to do my own research as to the pathway of blood test results, symptoms and the progression/knock on effects of having doctors who refuse to help. I have had to be extremely proactive in my own diagnosis, following the path of autoimmune conditions (co-morbid
Due to my ongoing failing health I've had to do my own research as to the pathway of blood test results, symptoms and the progression/knock on effects of having doctors who refuse to help. I have had to be extremely proactive in my own diagnosis, following the path of autoimmune conditions (co-morbid
Allywales8663
in
Pernicious Anaemia Society
1 month ago
Transitioning to Armour Thyroid
Hi everyone, I was diagnosed with an underactive thyroid at 21 and I've also got Hashimoto's. I recently changed from Levo/T3 to Armour, under the guidance of a lovely private endo, and I'm currently on three and a half grains per day, split into two doses. I wondered if anyone else has had side effects
Hi everyone, I was diagnosed with an underactive thyroid at 21 and I've also got Hashimoto's. I recently changed from Levo/T3 to Armour, under the guidance of a lovely private endo, and I'm currently on three and a half grains per day, split into two doses. I wondered if anyone else has had side effects
Jojozo
in
Thyroid UK
1 month ago
looking for next steps for my young husband
Out of desperation I am writing this -we are looking for nothing short of a miracle. My husband was diagnosed in 2021 at age 45 with Stage 4 Prostate Cancer. We have 3 small children ages 7,3 and 2 and we need something to give my husband time with his family. Sharing our journey in hopes that it can
Out of desperation I am writing this -we are looking for nothing short of a miracle. My husband was diagnosed in 2021 at age 45 with Stage 4 Prostate Cancer. We have 3 small children ages 7,3 and 2 and we need something to give my husband time with his family. Sharing our journey in hopes that it can
shaunaliz15
in
Advanced Prostate Cancer
6 months ago
Assistant Dogs.
I searched google a few years ago about assistant dogs because I thought I need one of them, but I got nowhere. Today I saw a demonstration of an assistant dog at work, it brought me to tears because it showed me just how much I do need one, how good , helpful it would be. I really think it would
I searched google a few years ago about assistant dogs because I thought I need one of them, but I got nowhere. Today I saw a demonstration of an assistant dog at work, it brought me to tears because it showed me just how much I do need one, how good , helpful it would be. I really think it would
saxcat
in
Fibromyalgia Action UK
1 month ago
RA and rashes
hi, I’m just wondering if you can get rashes with RA.. I’ve developed a few patches of small rashes possibly a bit like hives, though one is a circular rash (which aware could be ringworm but don’t think it is).. also aware these may just be fungal rashes. we have lupus in the family and although
hi, I’m just wondering if you can get rashes with RA.. I’ve developed a few patches of small rashes possibly a bit like hives, though one is a circular rash (which aware could be ringworm but don’t think it is).. also aware these may just be fungal rashes. we have lupus in the family and although
Sapphire1701
in
NRAS
1 month ago
PSA after one month on lupron
I am 63 with high risk PCa. I was diagnosed with PSA of 30 and Gleason 9 in December. Biopsy and MRI showed all 12 cores malignant with "likelihood of extra-capsular extension". PSMA PET scan showed no mets as of December 15. I began treatment on February 26 with a week of Casodex followed by a Lupron
I am 63 with high risk PCa. I was diagnosed with PSA of 30 and Gleason 9 in December. Biopsy and MRI showed all 12 cores malignant with "likelihood of extra-capsular extension". PSMA PET scan showed no mets as of December 15. I began treatment on February 26 with a week of Casodex followed by a Lupron
CavScout
in
Advanced Prostate Cancer
6 months ago
Lupus connected to Radiation
I recently read an article where someone felt that Lupus was connected to radiation exposure. Around 1989 I had a full radiation treatment for breast cancer. Back then they radiated your entire side back to front and I had horrific burns. 25 years later I was diagnosed with Sjogrens and Lupus. Has anyone
I recently read an article where someone felt that Lupus was connected to radiation exposure. Around 1989 I had a full radiation treatment for breast cancer. Back then they radiated your entire side back to front and I had horrific burns. 25 years later I was diagnosed with Sjogrens and Lupus. Has anyone
DogHospiceMom
in
LUPUS UK
1 month ago
Patient's view least important in diagnosis 🙄
Who'd have thought it? Research for Lupus Trust and in a Sjogren's UK newsletter but very applicable for us and others...https://academic.oup.com/rheumatology/advance-article/doi/10.1093/rheumatology/kead685/7473364?login=false UPDATE: larger photos of all three pages of the article uploaded below.
Who'd have thought it? Research for Lupus Trust and in a Sjogren's UK newsletter but very applicable for us and others...https://academic.oup.com/rheumatology/advance-article/doi/10.1093/rheumatology/kead685/7473364?login=false UPDATE: larger photos of all three pages of the article uploaded below.
Agitator23
in
Thyroid UK
1 month ago
After 25 years they have stopped my B12 - what can I do?
I'm in my early sixties. Generally very good health. On no medication. About twenty five years ago my then brilliant GP did a blood test for B12. A few days later rang me to come to the surgery immediately where he injected B12 himself. Apparently I had dangerously low levels of B12 that indicated I
I'm in my early sixties. Generally very good health. On no medication. About twenty five years ago my then brilliant GP did a blood test for B12. A few days later rang me to come to the surgery immediately where he injected B12 himself. Apparently I had dangerously low levels of B12 that indicated I
DIYenthusiast
in
Pernicious Anaemia Society
1 month ago
overactive to underactive
Hi Everyone, I’m a newbie to all this but i certainly need some advice as i feel like im in the dark with my doctors and endocrinologists i don’t exactly know anything apart from having an overactive thyroid which was treated for 18months then went into remission but came back 8months later then thyroid
Hi Everyone, I’m a newbie to all this but i certainly need some advice as i feel like im in the dark with my doctors and endocrinologists i don’t exactly know anything apart from having an overactive thyroid which was treated for 18months then went into remission but came back 8months later then thyroid
Leeleemarksy86
in
Thyroid UK
1 month ago
has anyone got Lupus in their eyes?
I have been told I have Lupus in my eyes. Does anyone else have this? Thank you
I have been told I have Lupus in my eyes. Does anyone else have this? Thank you
drobbie
in
LUPUS UK
1 month ago
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