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anti-MAG antibodies immunoglobulins
Hi and good morning I have a foot in both camps RA and Perifaral Neropathy. As two infusions of Rituxamab has not had any affect,depending on my blood test my Nuero Doc has mentioned(Not RA Doc) immunoglobulins? Also was mentioned another infusion which means attending Hospital several days running?☹️
Hi and good morning I have a foot in both camps RA and Perifaral Neropathy. As two infusions of Rituxamab has not had any affect,depending on my blood test my Nuero Doc has mentioned(Not RA Doc) immunoglobulins? Also was mentioned another infusion which means attending Hospital several days running?☹️
orange33
in
NRAS
5 years ago
Immunoglobulins anti-MAG antibodies ?periferal neuropathy
Hi there Vist to Neuro Doc was rather what I expected. The infusions I had haven't eased this condition. Had bloods done again to see if antibodies have reduced. Talk now of immunoglobulins ? What do that mean? Has any body had this treatment?
Hi there Vist to Neuro Doc was rather what I expected. The infusions I had haven't eased this condition. Had bloods done again to see if antibodies have reduced. Talk now of immunoglobulins ? What do that mean? Has any body had this treatment?
orange33
in
Neuropathy Support
5 years ago
Peripheral Neuropathy and MGUS
MG, which is very common,especially as we get older, is when the B cells in the bone marrow produce a clonal (abnormal)
immunoglobulin
protein known as a paraprotein.
MG, which is very common,especially as we get older, is when the B cells in the bone marrow produce a clonal (abnormal)
immunoglobulin
protein known as a paraprotein.
misswoosie
in
Foggy's "Invisible Illness" Support
5 years ago
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Help with Hughes/Aps and Symptoms
I have had a long battle with my health and was diagnosed with The big 3 By Prof Hughes (Lupus, sjrogens , Hughes) + Hashimoto's a while ago although he retired and I went to see another doctor that discounted his diagnosis, my results were as follows:- 3 x positive Anti Cardiolipin Ab's Anti Beta 2
I have had a long battle with my health and was diagnosed with The big 3 By Prof Hughes (Lupus, sjrogens , Hughes) + Hashimoto's a while ago although he retired and I went to see another doctor that discounted his diagnosis, my results were as follows:- 3 x positive Anti Cardiolipin Ab's Anti Beta 2
sloppydog
in
Hughes Syndrome APS Forum
5 years ago
I’m at my wits end
Hi I’m 26 and was diagnosed with FND approximately 2 and a half years ago. Initially I was admitted to hospital for 6 weeks of testing. The one thing they did find was calcification in my basal ganglia(responsible for initiating movement). During that stay it was believed I had stiff person syndrome
Hi I’m 26 and was diagnosed with FND approximately 2 and a half years ago. Initially I was admitted to hospital for 6 weeks of testing. The one thing they did find was calcification in my basal ganglia(responsible for initiating movement). During that stay it was believed I had stiff person syndrome
Stanleyleonard12
in
Functional Neurological Disorder - FND Hope
5 years ago
Bronchiectasis and low immunity
I feel like I've had a light bulb moment receiving my immunity blood test results today. I have low level of IgM and low levels of antibodies for haemophilus and pneumococcus. Having a quick Google it seems to make sense that I have developed bronchiectasis. My consultant has requested I get vaccinated
I feel like I've had a light bulb moment receiving my immunity blood test results today. I have low level of IgM and low levels of antibodies for haemophilus and pneumococcus. Having a quick Google it seems to make sense that I have developed bronchiectasis. My consultant has requested I get vaccinated
Treed12
in
Lung Conditions Community Forum
5 years ago
Help with Coeliac test results needed
The other results are:
Immunoglobulin
A : 3.98 g/L Range 0.7 - 4 g/L Tissue Transglutaminase IGA: 0.70 U/mL Range 0 - 10 U/mL Can I assume from these I'm not Coeliac and also I'm wondering if the 'only just normal' results indicate anything else I could look at? Thank you
The other results are:
Immunoglobulin
A : 3.98 g/L Range 0.7 - 4 g/L Tissue Transglutaminase IGA: 0.70 U/mL Range 0 - 10 U/mL Can I assume from these I'm not Coeliac and also I'm wondering if the 'only just normal' results indicate anything else I could look at? Thank you
msmono
in
Thyroid UK
5 years ago
missing heart beats that cause presyncope
I just hope it’s not down to free light chains and
immunoglobulin
BUT guess can dobble check my keratin on next blood test JUST make sure it’s not elevated given light chains seen with my microscope 🔬 n blood smear
I just hope it’s not down to free light chains and
immunoglobulin
BUT guess can dobble check my keratin on next blood test JUST make sure it’s not elevated given light chains seen with my microscope 🔬 n blood smear
Hidden
in
British Heart Foundation
5 years ago
APS positive but won’t diagnose
Hello everyone, I hope you all are well. So I tested positive for Cardiolipin IGM twice...very highly elevated levels...however my rheumatologist has advised she can’t diagnose me with APS because clinically I don’t fit the criteria (not enough miscarriages-I’ve had 2 miscarriages and I have two healthy
Hello everyone, I hope you all are well. So I tested positive for Cardiolipin IGM twice...very highly elevated levels...however my rheumatologist has advised she can’t diagnose me with APS because clinically I don’t fit the criteria (not enough miscarriages-I’ve had 2 miscarriages and I have two healthy
Anich78
in
Hughes Syndrome APS Forum
5 years ago
Secondary Sjögren’s Syndrome in Lupus Increases with Age
Secondary Sjögren’s Syndrome in Lupus Increases with Age Katie Robinson October 7, 2019 Lupus, Sjögren's Syndrome Sjögren’s syndrome secondary to systemic lupus erythematosus (SLE) rises in frequency with age, affects around one-quarter of all people with systemic lupus, and, despite less internal
Secondary Sjögren’s Syndrome in Lupus Increases with Age Katie Robinson October 7, 2019 Lupus, Sjögren's Syndrome Sjögren’s syndrome secondary to systemic lupus erythematosus (SLE) rises in frequency with age, affects around one-quarter of all people with systemic lupus, and, despite less internal
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 years ago
Blood count update
Hello my friends hoping you are all feeling better. I had my hemo appointment today and my immunoglobulins look like very low.... I will start new infusions in October! My leukocytes are 11.89, lymphocytes 5.49, erythrocytes 5.15 and platelets 119.Do you think things are getting better, help!
Hello my friends hoping you are all feeling better. I had my hemo appointment today and my immunoglobulins look like very low.... I will start new infusions in October! My leukocytes are 11.89, lymphocytes 5.49, erythrocytes 5.15 and platelets 119.Do you think things are getting better, help!
Deta1961
in
CLL Support
5 years ago
Just arrived!
I was diagnosed with CLL in 2008, at the age of 57. After 2 years of watch-and-wait I was referred to King’s College Hospital in London and had FCminiR chemo (Arctic Trial) over a 9 month period. I was able to work full time until the end of 2013, and have taught short courses on and off since then.
I was diagnosed with CLL in 2008, at the age of 57. After 2 years of watch-and-wait I was referred to King’s College Hospital in London and had FCminiR chemo (Arctic Trial) over a 9 month period. I was able to work full time until the end of 2013, and have taught short courses on and off since then.
Salvoboy
in
CLL Support
5 years ago
Problems with Neulasta after IVIG and in Ibrutinib
Neutrophils dropped over the last couple of months while on IBN so my doctors gave me a shot of Neulasta. I have ended up with weeks or achy bones, problems breathing, enhanced neuropathy and mouth sores, which are like blood blisters. My experience is that I have had lots of side effects from every
Neutrophils dropped over the last couple of months while on IBN so my doctors gave me a shot of Neulasta. I have ended up with weeks or achy bones, problems breathing, enhanced neuropathy and mouth sores, which are like blood blisters. My experience is that I have had lots of side effects from every
KevinCLLITP
in
CLL Support
5 years ago
update on my quest.
Hi, sorry it has been a while, I have now had my second appointment at Derriford and a lovely letter from Guys and ST Thomas'. The letter stated that as I have had 3 consecutive miscarriages and that I have an anticardiolipin antibody of Igm, that fulfilled the criteria for obstetric antiphospholipid
Hi, sorry it has been a while, I have now had my second appointment at Derriford and a lovely letter from Guys and ST Thomas'. The letter stated that as I have had 3 consecutive miscarriages and that I have an anticardiolipin antibody of Igm, that fulfilled the criteria for obstetric antiphospholipid
pinkyandperky
in
Hughes Syndrome APS Forum
5 years ago
anyone with Low IG M
Shipment of
immunoglobulin
is back in USA. Will be getting it soon. Have no energy. Really appreciate this group and would love feedback. Thanks to everyone here for having shared in such a heartfelt way.
Shipment of
immunoglobulin
is back in USA. Will be getting it soon. Have no energy. Really appreciate this group and would love feedback. Thanks to everyone here for having shared in such a heartfelt way.
nanno
in
LUPUS UK
5 years ago
Free Light Chain Deposoataion Cystic Lung Diease
I think it’s disgusting HOW powers that Be researchers are leaving people to suffer LIGHT chain deposit diease’s How many have heard of FREE light chain Deposation Cystic Lung Diease. Guess you could say it’s TAD like CF and BRONCHIATASIAS but yall never hear blf talk about light chain lung disease
I think it’s disgusting HOW powers that Be researchers are leaving people to suffer LIGHT chain deposit diease’s How many have heard of FREE light chain Deposation Cystic Lung Diease. Guess you could say it’s TAD like CF and BRONCHIATASIAS but yall never hear blf talk about light chain lung disease
Hidden
in
Lung Conditions Community Forum
5 years ago
Advice on confusing results
Immunoglobulin
A level 2.04 g/L [0.65 - 4.21] Serum vitamin B12 level 268 ng/L [187.0 - 883.0] Serum folate level 8.2 ug/L [3.1 - 20.0] Serum total 25-hydroxy vitamin D level 45 Serum TSH level 2.9 miu/L [0.35 - 4.94] Notes: B12 has increased slightly from 18th April when it was 230 ng/L.
Immunoglobulin
A level 2.04 g/L [0.65 - 4.21] Serum vitamin B12 level 268 ng/L [187.0 - 883.0] Serum folate level 8.2 ug/L [3.1 - 20.0] Serum total 25-hydroxy vitamin D level 45 Serum TSH level 2.9 miu/L [0.35 - 4.94] Notes: B12 has increased slightly from 18th April when it was 230 ng/L.
ILR2019
in
Thyroid UK
5 years ago
Concerned about thick phlegm waking me up at night
One thing is concerning me, my Glucose level is 108 H,
IMMUNOGLOBULIN
G 577 and
IMMUNOGLOBULIN
M 46. In addition, I have been awaken often with thick phlegm in my mouth, usually white but sometimes black.
One thing is concerning me, my Glucose level is 108 H,
IMMUNOGLOBULIN
G 577 and
IMMUNOGLOBULIN
M 46. In addition, I have been awaken often with thick phlegm in my mouth, usually white but sometimes black.
Michael199
in
CLL Support
5 years ago
IGA deficiency and celiac disease
When I turned 23, a blood test came back with these results (I was eating gluten):
IMMUNOGLOBULIN
A: 0.58 g/L (0.70-4.00) Gliadin Antibodies (IgG): 0.3 U/ml (Negative: <7 / Equivocal 7-10 / Positive >10) Gliadin Antibodies (IgA): 0.0 U/ml (Negative: <7 / Equivocal 7-10 / Positive >10) Tissue Transglutaminase
When I turned 23, a blood test came back with these results (I was eating gluten):
IMMUNOGLOBULIN
A: 0.58 g/L (0.70-4.00) Gliadin Antibodies (IgG): 0.3 U/ml (Negative: <7 / Equivocal 7-10 / Positive >10) Gliadin Antibodies (IgA): 0.0 U/ml (Negative: <7 / Equivocal 7-10 / Positive >10) Tissue Transglutaminase
dannyhashimotos
in
Thyroid UK
5 years ago
Does Anti-phosphatidylserine = APS diagnosis?
Hello! I could really use some direction. (Located in US). I tested positive - twice - for anti-phosphatidylserine IgM (32 and 53). I tested negative for the three “standard” labs. I had a knee to pelvis DVT two years ago. The hematologist at that time told me it was the Pill. She pulled all
Hello! I could really use some direction. (Located in US). I tested positive - twice - for anti-phosphatidylserine IgM (32 and 53). I tested negative for the three “standard” labs. I had a knee to pelvis DVT two years ago. The hematologist at that time told me it was the Pill. She pulled all
ChicagoCubs
in
Hughes Syndrome APS Forum
5 years ago
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