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Parietal cell antibody test
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labs results that contraindicate one another
Prior to starting any injections my
parietal
cell
antibody
test
was positive but completely normal gastrin - I would assume gastrin would be high as my new dr suspects PA.
Prior to starting any injections my
parietal
cell
antibody
test
was positive but completely normal gastrin - I would assume gastrin would be high as my new dr suspects PA.
Katep66875
in
Pernicious Anaemia Society
3 months ago
Given Private Diagnosis But Antibody Test Is Negative? A Little Confused.
He recommended I get a
parietal
cell
antibody
test
. Now for the confusion and uncertainty created in me. I requested a PCA antibody test from my GP who text me to inform me that the lab does not do it instead they do an Autoimmune Profile. This came back negative.
He recommended I get a
parietal
cell
antibody
test
. Now for the confusion and uncertainty created in me. I requested a PCA antibody test from my GP who text me to inform me that the lab does not do it instead they do an Autoimmune Profile. This came back negative.
B12again
in
Pernicious Anaemia Society
2 days ago
Given Private Diagnosis But Antibody Test Is Negative?
He recommended I get a
parietal
cell
antibody
test
. Now for the confusion and uncertainty created in me. I requested a PCA antibody test from my GP who text me to inform me that the lab does not do it instead they do an Autoimmune Profile. This came back negative.
He recommended I get a
parietal
cell
antibody
test
. Now for the confusion and uncertainty created in me. I requested a PCA antibody test from my GP who text me to inform me that the lab does not do it instead they do an Autoimmune Profile. This came back negative.
B12again
in
Thyroid UK
2 days ago
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B12 how much and how often
Finally from Israel I was advised to get the Intrinsic Factor
Antibody
Blood
Test
and the
Parietal
Cell
Antibody
Blood
Test
. Pernicious Anemia. I have to take a shot of Methylcobalamin daily.
Finally from Israel I was advised to get the Intrinsic Factor
Antibody
Blood
Test
and the
Parietal
Cell
Antibody
Blood
Test
. Pernicious Anemia. I have to take a shot of Methylcobalamin daily.
Jeep13
in
Pernicious Anaemia Society
1 month ago
How often to Self Inject
She also had a homocysteine test that came back low, so the docs said she did not need the
parietal
cell
antibody
test
because of that. Do you all think she should definitely have the test for parietal cell antibodies as well to rule it out or am I being too paranoid?
She also had a homocysteine test that came back low, so the docs said she did not need the
parietal
cell
antibody
test
because of that. Do you all think she should definitely have the test for parietal cell antibodies as well to rule it out or am I being too paranoid?
MrJustatip
in
Pernicious Anaemia Society
11 months ago
Gastric Parietal Cell Antibody
Just wondering whether any members have had this test? I'm not really thinking about those who have had a B12 deficiency (or suspected Pernicious Anaemia) followed up by this test. Rather has anyone had done spontaneously as the link below [i]appears[/i] to imply. As I read it, the words say GPC should
Just wondering whether any members have had this test? I'm not really thinking about those who have had a B12 deficiency (or suspected Pernicious Anaemia) followed up by this test. Rather has anyone had done spontaneously as the link below [i]appears[/i] to imply. As I read it, the words say GPC should
helvella
Thyroid UK
in
Thyroid UK
2 months ago
Positive IFA, Negative Parietal Cell, B-12 injections affect IFA test
Hello, I recently tested positive for intrinsic factor blocking
antibody
but the result of my
parietal
cell
antibody
test
was negative. I’m curious if other members have had this same experience? My doctors have suspected a PA diagnosis for several years.
Hello, I recently tested positive for intrinsic factor blocking
antibody
but the result of my
parietal
cell
antibody
test
was negative. I’m curious if other members have had this same experience? My doctors have suspected a PA diagnosis for several years.
mcg-woo
in
Pernicious Anaemia Society
1 year ago
Son tested positive for gastric parietal cell antibodies
His b12 wasn't checked but his gastric
parietal
cell
antibody
was positive. His allergy
test
was also high, which they now want test further for. Does having gastric parietal cell antibodies, always mean pernicious aneamia?
His b12 wasn't checked but his gastric
parietal
cell
antibody
was positive. His allergy
test
was also high, which they now want test further for. Does having gastric parietal cell antibodies, always mean pernicious aneamia?
fatfatfat
in
Pernicious Anaemia Society
4 months ago
Haematologists consultant
Hi I’ve been trying to get help with my Pernicious anemia diagnosis which my mum & sister had they have both passed away now, but the drs are not helping I only got diagnosed through me asking for further tests after they initially told me my B12 was high 2000 so I wasn’t deficient!! , my dr didn’t
Hi I’ve been trying to get help with my Pernicious anemia diagnosis which my mum & sister had they have both passed away now, but the drs are not helping I only got diagnosed through me asking for further tests after they initially told me my B12 was high 2000 so I wasn’t deficient!! , my dr didn’t
Windyway
in
Pernicious Anaemia Society
5 months ago
Blood Work
Hello Friends, I asked this question on my original thread but someone suggested I start a new one. I was diagnosed with Autoimmune Atrophic Gastritis 2 weeks ago and have been having a hard time mentally . My family Dr this past Friday sends me the blood tests results and says they cannot comment
Hello Friends, I asked this question on my original thread but someone suggested I start a new one. I was diagnosed with Autoimmune Atrophic Gastritis 2 weeks ago and have been having a hard time mentally . My family Dr this past Friday sends me the blood tests results and says they cannot comment
Canadian77
in
Pernicious Anaemia Society
5 months ago
Request for experiences with Vitamin D
If anyone of you would be willing to share your personal experience with Vitamin D that would be appreciated. All good with what is thought to be true in the medicial field I am well versed in that angle. I have taken D3 with K2 and the results were not definitive so I discontinued. I have lived
If anyone of you would be willing to share your personal experience with Vitamin D that would be appreciated. All good with what is thought to be true in the medicial field I am well versed in that angle. I have taken D3 with K2 and the results were not definitive so I discontinued. I have lived
WIZARD6787
in
Pernicious Anaemia Society
17 days ago
NICE: Teprotumumab for treating thyroid eye disease ID 6432 - being scoped
I have just noticed a new NICE guideline has been started. Only a skeleton at present - in the guideline scoping state. It will probably be years before it is completed. It is good that it has been selected for further work but must be devastating for anyone suffering TED to see how far away this (potential
I have just noticed a new NICE guideline has been started. Only a skeleton at present - in the guideline scoping state. It will probably be years before it is completed. It is good that it has been selected for further work but must be devastating for anyone suffering TED to see how far away this (potential
helvella
Thyroid UK
in
Thyroid UK
4 months ago
Polyneuropathy.
I treat my polyneuropathy with B6 and B12. GracePV shared their experience with B6, B12 nd B1. This inspired me to revisit my self treatment of my polyneuropathy. I came across information about Benfotiamine which is similar to Thiamine Hydrochloride and Thiamine Nitrate. There are indications
I treat my polyneuropathy with B6 and B12. GracePV shared their experience with B6, B12 nd B1. This inspired me to revisit my self treatment of my polyneuropathy. I came across information about Benfotiamine which is similar to Thiamine Hydrochloride and Thiamine Nitrate. There are indications
WIZARD6787
in
Pernicious Anaemia Society
4 months ago
I got my results back for pernicious anemia! Looks like folate deficiency, but would really appreciate any comments
I finally got my blood test results back for pernicious anemia. It looks like I don't have it, and that my problem is folate deficiency. And low reticulocyte count which would be caused by low folate I suppose. My other results are all in range, though active B12 could maybe be higher I am thinking
I finally got my blood test results back for pernicious anemia. It looks like I don't have it, and that my problem is folate deficiency. And low reticulocyte count which would be caused by low folate I suppose. My other results are all in range, though active B12 could maybe be higher I am thinking
Carrie234
in
Pernicious Anaemia Society
24 days ago
Autologous Cell Transplants - Promising Clinical Trial Getting Underway
August 7,2024 article from Scitechdaily.com Breakthrough Parkinson’s Treatment Enters Human Trials After Primate Success TOPICS:BrainNeuroscienceParkinson's DiseaseUniversity Of Wisconsin-Madison By UNIVERSITY OF WISCONSIN-MADISON AUGUST 7, 2024 A clinical trial has begun to offer a new treatment
August 7,2024 article from Scitechdaily.com Breakthrough Parkinson’s Treatment Enters Human Trials After Primate Success TOPICS:BrainNeuroscienceParkinson's DiseaseUniversity Of Wisconsin-Madison By UNIVERSITY OF WISCONSIN-MADISON AUGUST 7, 2024 A clinical trial has begun to offer a new treatment
Shorebirdsotherhalf
in
Cure Parkinson's
15 days ago
What is the difference between these two tests?
Parietal Cell Antibody, ELISA/ positive Parietal Cell Antibody with Relex to Titer/ Negative
Parietal Cell Antibody, ELISA/ positive Parietal Cell Antibody with Relex to Titer/ Negative
Tigerlilly81
in
Pernicious Anaemia Society
1 year ago
New results - opinions please
Hi all, Got my bloods done again. For this round I was taking 100mcg of levo monday - friday and then 75mcg on the weekend. Other things I'm taking are: - Omega 3 supplement - 50 mcg B12 - 3000iu vitamin D The dr has now put me on 100mcg for all days of the week: [u]
Thyroid
[/u] Free Thyroxine
Hi all, Got my bloods done again. For this round I was taking 100mcg of levo monday - friday and then 75mcg on the weekend. Other things I'm taking are: - Omega 3 supplement - 50 mcg B12 - 3000iu vitamin D The dr has now put me on 100mcg for all days of the week: [u]
Thyroid
[/u] Free Thyroxine
Griffo_
in
Thyroid UK
19 days ago
Hello - I'm interested in other GCA experiences
Hi. First time I've posted. I was diagnosed with GCA in February 2024 following hospital admission. It took medics a while to work it out but, once they did and started me on Prednisolone, my symptoms quickly improved. I returned to work early April and things seemed to be going in the right direction
Hi. First time I've posted. I was diagnosed with GCA in February 2024 following hospital admission. It took medics a while to work it out but, once they did and started me on Prednisolone, my symptoms quickly improved. I returned to work early April and things seemed to be going in the right direction
BladesLover
in
PMRGCAuk
18 days ago
I feel weird after taking meconerv forte and ginsomin. Is it advisable to continue combining them with ligaba?
I have been on ulcer drugs for years. My latest symptoms made my doctor place me on pariet, meconerv forte, ginsomin, melotamin and ligaba. I discovered that I feel very low mood after taking the drugs. Stomach, chaste, waist and back pains; insomnia, muscle twitching, tingling sensation, lethargy, fatigue
I have been on ulcer drugs for years. My latest symptoms made my doctor place me on pariet, meconerv forte, ginsomin, melotamin and ligaba. I discovered that I feel very low mood after taking the drugs. Stomach, chaste, waist and back pains; insomnia, muscle twitching, tingling sensation, lethargy, fatigue
Orimini
in
Pernicious Anaemia Society
1 year ago
Life after Tocilizumab?
I've been off steroids since mid-May. Continuing to take methotrexate (15mg weekly) and Toxilizumab weekly. I seem to be doing well - bloods fine and health ok. I'm seeing rheumatologist next week and my concern is I'm guessing that I won't be eligible for further Tox after my current prescription runs
I've been off steroids since mid-May. Continuing to take methotrexate (15mg weekly) and Toxilizumab weekly. I seem to be doing well - bloods fine and health ok. I'm seeing rheumatologist next week and my concern is I'm guessing that I won't be eligible for further Tox after my current prescription runs
tweety_pie
in
PMRGCAuk
2 months ago
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