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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
28 days 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
8 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
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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
1 month 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
3 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
3 months 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
GP refusing to offer IFAB Test
I recently requested and Intrinsic Factor Antibody test with my GP and was told there's no need to do this
test
if my
Parietal
Cell
antibody
test
was negative/normal. The
Parietal
Cell
test was done in Jan 2021 and I assumed the IFAB was done at the same time and also came back normal.
I recently requested and Intrinsic Factor Antibody test with my GP and was told there's no need to do this
test
if my
Parietal
Cell
antibody
test
was negative/normal. The
Parietal
Cell
test was done in Jan 2021 and I assumed the IFAB was done at the same time and also came back normal.
cloudspotting
in
Pernicious Anaemia Society
2 years 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
2 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
2 months 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
10 months ago
Just been approved for Vitamin B12 injection treatment.
My doctor was reluctant for whatever reason to authorize the injections, even though I had a positive
parietal
cell
antibody
test
. I guess my question is. Im due to start my treatment a week from Monday. Three loading dose injections for the first 2 weeks, then 1 very 3 months for life.
My doctor was reluctant for whatever reason to authorize the injections, even though I had a positive
parietal
cell
antibody
test
. I guess my question is. Im due to start my treatment a week from Monday. Three loading dose injections for the first 2 weeks, then 1 very 3 months for life.
MikeyO
in
Pernicious Anaemia Society
2 years ago
Can b12 be administered together with proton pump inhibitors?
I have been treated for years now for stomach ulcer without good relief. Two years ago, I underwent endoscopy test. The results showed some healed ulcer and some erosion which resulted to inflammation. The doctor said I had gastritis. He bombarded my system with antibiotics and proton pump inhibitors
I have been treated for years now for stomach ulcer without good relief. Two years ago, I underwent endoscopy test. The results showed some healed ulcer and some erosion which resulted to inflammation. The doctor said I had gastritis. He bombarded my system with antibiotics and proton pump inhibitors
Orimini
in
Pernicious Anaemia Society
10 months ago
PV & Gene Editing for Sickle cell anemia
Has anyone been following the latest news on treatment for sickle cell anemia? Since many of us are treated with hydroxyurea which is approved for sickle cell anemia, I was wondering if this may be in our future? "The F.D.A. approved the first gene editing therapy ever, for sickle cell disease, a debilitating
Has anyone been following the latest news on treatment for sickle cell anemia? Since many of us are treated with hydroxyurea which is approved for sickle cell anemia, I was wondering if this may be in our future? "The F.D.A. approved the first gene editing therapy ever, for sickle cell disease, a debilitating
ERei
in
MPN Voice
6 months ago
parietal cell antibody lab results
I’m having trouble interpreting my lab results. My Parietal Cell Antibody IgG value is 33.2 units and it said the standard range is 0.0-24.9 units. So it’s above the standard range but not by much. Apparently above 25 units is positive so that means I’m positive? I just want to confirm.
I’m having trouble interpreting my lab results. My Parietal Cell Antibody IgG value is 33.2 units and it said the standard range is 0.0-24.9 units. So it’s above the standard range but not by much. Apparently above 25 units is positive so that means I’m positive? I just want to confirm.
Purplegirl2
in
Pernicious Anaemia Society
1 year ago
Returning temporal headaches after stopping Tocilizumab, what to do ?
I will try to be brief. UK male aged 70 Diagnosed with GCA (ultra sound scan only) 2 years ago. Only minor symptoms experienced (mainly temporal headache). 65mg Prednisolone prescribed daily for 2 weeks, then to reduce by 5mg per month. A couple of "flares" (just headaches) in the following 12 months
I will try to be brief. UK male aged 70 Diagnosed with GCA (ultra sound scan only) 2 years ago. Only minor symptoms experienced (mainly temporal headache). 65mg Prednisolone prescribed daily for 2 weeks, then to reduce by 5mg per month. A couple of "flares" (just headaches) in the following 12 months
ghost123uk
in
PMRGCAuk
12 days ago
Qualifying for Tocilizumab
Hello, I have had a relapse of GCA and have been put on a reduction plan. Was on 40mg pred now reducing by 10mg every two weeks. I had an emergency ultrasound of temporal and axillary arteries but it was three weeks after going on 40mg of pred so my consultant radiologist did say that nothing would
Hello, I have had a relapse of GCA and have been put on a reduction plan. Was on 40mg pred now reducing by 10mg every two weeks. I had an emergency ultrasound of temporal and axillary arteries but it was three weeks after going on 40mg of pred so my consultant radiologist did say that nothing would
Golfers1
in
PMRGCAuk
24 days ago
Coopersmummy7
Hi,I am new to this awful condition.Had nearly a year of being undiagnosed and finally rushed into hospital Dec.22 with GCAand loss of sight in one eye.Long story short,2 relapses,yo yo ing of f prednisilone,could not tolerate Metho, or leflunomide,and now looks like I will be starting on Tocilzumab.Am
Hi,I am new to this awful condition.Had nearly a year of being undiagnosed and finally rushed into hospital Dec.22 with GCAand loss of sight in one eye.Long story short,2 relapses,yo yo ing of f prednisilone,could not tolerate Metho, or leflunomide,and now looks like I will be starting on Tocilzumab.Am
Angelsmummy
in
PMRGCAuk
2 months ago
Vasculitus, a promising road ahead- let’s hope so!
https://www.thelancet.com/journals/lanrhe/article/PIIS2665-9913(24)00094-8/fulltext?dgcid=raven_jbs_aip_email ‘…Biologics have come to the forefront as glucocorticoid-sparing agents. After the seminal GiACTA trial, tocilizumab is now recommended as a first-line therapy for giant cell arteritis in combination
https://www.thelancet.com/journals/lanrhe/article/PIIS2665-9913(24)00094-8/fulltext?dgcid=raven_jbs_aip_email ‘…Biologics have come to the forefront as glucocorticoid-sparing agents. After the seminal GiACTA trial, tocilizumab is now recommended as a first-line therapy for giant cell arteritis in combination
Exflex
in
PMRGCAuk
2 months ago
Question on PMR and Temporal Arteritis
Does anyone know: would an MRI show Temporal Arteritis or would a person need a biopsy to determine if Temporal Arteritis was present? Asking for a person newly diagnosed with PMR and in the ER dept was told she had Temporal Arteritis. Yesterday she went to the rheumatologist and was told she definitely
Does anyone know: would an MRI show Temporal Arteritis or would a person need a biopsy to determine if Temporal Arteritis was present? Asking for a person newly diagnosed with PMR and in the ER dept was told she had Temporal Arteritis. Yesterday she went to the rheumatologist and was told she definitely
Musiclady18
in
PMRGCAuk
2 months ago
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