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AMAs but normal bloodwork
I had written a couple of posts awhile back when I had AMAs in my blood and was waiting for follow- up bloodwork. I am posting my results from Nov. 8th so that anyone in my situation can see. I had high Alt in July because of Alcohol use. The dr did extra blood tests and I had AMAs in my blood. I
I had written a couple of posts awhile back when I had AMAs in my blood and was waiting for follow- up bloodwork. I am posting my results from Nov. 8th so that anyone in my situation can see. I had high Alt in July because of Alcohol use. The dr did extra blood tests and I had AMAs in my blood. I
SSMPCW123
in
PBC Foundation
7 years ago
I'm new here - and glad I'm probably not crazy afterall
Hi, I've been following this support group for a few months now and have learned so much about Hughe's Syndrome. My story is long (like most everyone's) and I hope you can bare with me. I am 51 years old and live in Missouri - USA. I had never heard about Hughe's Syndrome until I had blood work
Hi, I've been following this support group for a few months now and have learned so much about Hughe's Syndrome. My story is long (like most everyone's) and I hope you can bare with me. I am 51 years old and live in Missouri - USA. I had never heard about Hughe's Syndrome until I had blood work
Tyler3
in
Hughes Syndrome APS Forum
7 years ago
May be starting to get somewhere...
After a coeliac screen was done to check if that might be the cause of the recurring low ferritin it showed I had a low IgA. This led to all my immunoglobulin levels being checked and all coming back below range. IgA 0.20 (0.8 - 4.0 g/L) IgG 3.65 (5.5 - 16.5 g/L) IgM 0.24 (0.4 - 2.0 g/L) I’m not
After a coeliac screen was done to check if that might be the cause of the recurring low ferritin it showed I had a low IgA. This led to all my immunoglobulin levels being checked and all coming back below range. IgA 0.20 (0.8 - 4.0 g/L) IgG 3.65 (5.5 - 16.5 g/L) IgM 0.24 (0.4 - 2.0 g/L) I’m not
TheMaybeGirl
in
Foggy's "Invisible Illness" Support
7 years ago
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Arguing With Lung Doctor
Why WELL 3 rotten inhalers AND nebuliser and standerd atibiotcs is best all lung care involves WELL he said thats best NHS lung care gets and this nothing else. Well i disagreed AND said if thats what you belive thats whats up with lung care. So asked him about my IGM antibodes only to be told things
Why WELL 3 rotten inhalers AND nebuliser and standerd atibiotcs is best all lung care involves WELL he said thats best NHS lung care gets and this nothing else. Well i disagreed AND said if thats what you belive thats whats up with lung care. So asked him about my IGM antibodes only to be told things
Hidden
in
Lung Conditions Community Forum
7 years ago
Recent PBC diagnosis
Hi I was diagnosed with PBC in July after 3 years of raised liver enzymes and tiredness and itching, this was all put down to stress and the menopause as well as being treated for scabies 3 time lol also shift work as I’m a paramedic, I changed GP’s and was referred to Gastro at Hospital had lots of
Hi I was diagnosed with PBC in July after 3 years of raised liver enzymes and tiredness and itching, this was all put down to stress and the menopause as well as being treated for scabies 3 time lol also shift work as I’m a paramedic, I changed GP’s and was referred to Gastro at Hospital had lots of
Rozm2004
in
PBC Foundation
7 years ago
Candida?
My journey has been long since my first experience with the stomach virus. Many twists and turns and very unfortunate (and unbelievable) events have transpired. Doctors have randomly chose drugs that all seemed to make things dramatically worse (predisone, cortical steroids, antibiotic regiments, protonix
My journey has been long since my first experience with the stomach virus. Many twists and turns and very unfortunate (and unbelievable) events have transpired. Doctors have randomly chose drugs that all seemed to make things dramatically worse (predisone, cortical steroids, antibiotic regiments, protonix
Hidden
in
Anxiety Support
7 years ago
Help needed with diagnosis
Hi there I’ve been fighting with my health now on and off for about 13 yrs, I always get sent to a neurologist but after having some blood test done and looking at the results on line and what it could mean I came across lupus, and found a list of symptoms that match what I’m going through but have never
Hi there I’ve been fighting with my health now on and off for about 13 yrs, I always get sent to a neurologist but after having some blood test done and looking at the results on line and what it could mean I came across lupus, and found a list of symptoms that match what I’m going through but have never
Tinks19790
in
LUPUS UK
7 years ago
Casein intolerance from cows and goats?
Hi all Been on a big journey with my health that can be summed up in drs finding nothing wrong through tests and concluding it's likely cfs/fibromyalgia. However it's my health and I'm convinced it's something. Through trial and error (I.e excluding from my diet) I have found what I think is an issue
Hi all Been on a big journey with my health that can be summed up in drs finding nothing wrong through tests and concluding it's likely cfs/fibromyalgia. However it's my health and I'm convinced it's something. Through trial and error (I.e excluding from my diet) I have found what I think is an issue
steviep43
in
Healthy Eating
7 years ago
AMAs in blood no other tests show it
I posted a few weeks ago and received reassuring replies. I wanted to post again to see if anyone had anymore information for me. I am in Virginia, USA I had AMAs in blood. My alt and ast were a little high in July because of drinking. On Sept. 12th everything was in the normal range; alt, ast, alp
I posted a few weeks ago and received reassuring replies. I wanted to post again to see if anyone had anymore information for me. I am in Virginia, USA I had AMAs in blood. My alt and ast were a little high in July because of drinking. On Sept. 12th everything was in the normal range; alt, ast, alp
SSMPCW123
in
PBC Foundation
7 years ago
Very high RF & symptoms, can anyone relate / have gotten diagnosis?
Hello everyone. As the question says, I'm interested to see if anyone can relate to what I'm experiencing and what diagnosis has been given. So, I have an elevated RF latex test of 450 (tested twice) and IgM that is 3.1 (above normal). I also have an elevated calprotectin of 90. Just some info that
Hello everyone. As the question says, I'm interested to see if anyone can relate to what I'm experiencing and what diagnosis has been given. So, I have an elevated RF latex test of 450 (tested twice) and IgM that is 3.1 (above normal). I also have an elevated calprotectin of 90. Just some info that
WK1010
in
NRAS
7 years ago
I am sleepy every second of my life
Hello. I haven't been diagnosed with fibro, I'm just posting here because maybe someone can relate or help me. What could cause me to be sleepy every single second? I've got a positive rheumatoid factor of 450 and IgM of 3.1 and calprotectin of 90. I am going back and forth to the hospital for evaluation
Hello. I haven't been diagnosed with fibro, I'm just posting here because maybe someone can relate or help me. What could cause me to be sleepy every single second? I've got a positive rheumatoid factor of 450 and IgM of 3.1 and calprotectin of 90. I am going back and forth to the hospital for evaluation
WK1010
in
Fibromyalgia Action UK
7 years ago
Low IgG and low IgM
I have just been told I have the above. I'm hypothyroid on 100 of Levo. I'm sick with worry could there be a correlation? So grateful for any advice
I have just been told I have the above. I'm hypothyroid on 100 of Levo. I'm sick with worry could there be a correlation? So grateful for any advice
Cazzalouise
in
Thyroid UK
7 years ago
Just waiting blood test results very anxioud
Still waiting diagnosis . Saw professor Pinzani at the at the Royal free. He is so very kind and caring . He even stayed with me when my bloods were taken . He booked me in for a fibro scan then and there . I was the higher. end of normal . 6. 5 was mentioned and 12 . There is some moderate fibrosis
Still waiting diagnosis . Saw professor Pinzani at the at the Royal free. He is so very kind and caring . He even stayed with me when my bloods were taken . He booked me in for a fibro scan then and there . I was the higher. end of normal . 6. 5 was mentioned and 12 . There is some moderate fibrosis
Mirimaur
in
PBC Foundation
7 years ago
Blood results terrifying
Hi. Just got my blood test results back. So I have high PLT, Eosinophil, Alkaline Phosphatase, Alanine Transaminase, and Igm. I don't understand any of this. Are these connected to PBC?
Hi. Just got my blood test results back. So I have high PLT, Eosinophil, Alkaline Phosphatase, Alanine Transaminase, and Igm. I don't understand any of this. Are these connected to PBC?
SharonM69
in
PBC Foundation
7 years ago
very confused..
As you all know im going to see dr kaul at the london bridge lupus centre the end of this month. Well i have requested a letter and old bloods from my nhs rhumy and recieved them on friday - The letter he has wrote for me to take i wont be giving the new hospital as his basically saying he doesnt want
As you all know im going to see dr kaul at the london bridge lupus centre the end of this month. Well i have requested a letter and old bloods from my nhs rhumy and recieved them on friday - The letter he has wrote for me to take i wont be giving the new hospital as his basically saying he doesnt want
Hidden
in
LUPUS UK
7 years ago
Autoimmune hepatitis scare
I'm new to this forum and think it's great. My problem: My GP just told me I probably have autoimmune hepatitis as my GGT is 107, IgM is 5.55, Mitochondrial Ab is positive, and Mitochondrial Ab Titre 1:640. She gave me the impression that I have a much shortened lifespan and will spend the rest of what
I'm new to this forum and think it's great. My problem: My GP just told me I probably have autoimmune hepatitis as my GGT is 107, IgM is 5.55, Mitochondrial Ab is positive, and Mitochondrial Ab Titre 1:640. She gave me the impression that I have a much shortened lifespan and will spend the rest of what
Carly92
in
British Liver Trust
7 years ago
So confused, would love your opinions
This afternoon I had my second appt. with my hepatic specialist. I am so confused and hoping some of you can chime in. Current labs are back and my two mitochondrial tests are still positive (titer is 1:80 and AB serum is positive), I have 3 positive AFP tests from two different labs and I just had an
This afternoon I had my second appt. with my hepatic specialist. I am so confused and hoping some of you can chime in. Current labs are back and my two mitochondrial tests are still positive (titer is 1:80 and AB serum is positive), I have 3 positive AFP tests from two different labs and I just had an
angelofeventide
in
PBC Foundation
7 years ago
High E.S.R
Hi, I was at risk of Lyme disease, I was on amoxicillin for 10 days, i have finished course 2 weeks ago, Fortunately I have no Lyme disease, all symptoms was just reaction of tick bite. Analysis for ELISA IgM and IgG are negative. Everything in My blood test are OK, except E.S.R. It is getting high
Hi, I was at risk of Lyme disease, I was on amoxicillin for 10 days, i have finished course 2 weeks ago, Fortunately I have no Lyme disease, all symptoms was just reaction of tick bite. Analysis for ELISA IgM and IgG are negative. Everything in My blood test are OK, except E.S.R. It is getting high
teona
in
NRAS
7 years ago
Context change
Does anyone know how to change from CLL community to Waldenstroms? I was placed in CLL because it was the category I was looking at when I decided to join. I really am one who keeps track of IgM level
Does anyone know how to change from CLL community to Waldenstroms? I was placed in CLL because it was the category I was looking at when I decided to join. I really am one who keeps track of IgM level
Bbonal
in
CLL Support
7 years ago
FCR after four years
When I was taken to the hospital with HB of 5.4 and Leukos 20.0 and lots of wrong b Cells, this was 9/2013, I had only little hope to recover again, as I was tested unmutated, CD 38 neg and ZAP 70 of 50% and Trisomie 12. I received 13 packs of Erytrocyt/Concentrate and 6 rounds of FCR. Only minor sideeffects
When I was taken to the hospital with HB of 5.4 and Leukos 20.0 and lots of wrong b Cells, this was 9/2013, I had only little hope to recover again, as I was tested unmutated, CD 38 neg and ZAP 70 of 50% and Trisomie 12. I received 13 packs of Erytrocyt/Concentrate and 6 rounds of FCR. Only minor sideeffects
seoul
in
CLL Support
7 years ago
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