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Finally, I’ve been diagnosed!
I had my follow up appointment yesterday with the Rheumatologist he had previously requested tests for ANA, Rheumatoid factor, CCP antibodies, Serum immunoglobulins, urine for Bence Jones protein, ESR and CPR, vitamin D level , Myeloma screen, X-rays on both hands and wrists and ultrasound scans of the
I had my follow up appointment yesterday with the Rheumatologist he had previously requested tests for ANA, Rheumatoid factor, CCP antibodies, Serum immunoglobulins, urine for Bence Jones protein, ESR and CPR, vitamin D level , Myeloma screen, X-rays on both hands and wrists and ultrasound scans of the
Leepeelee
in
PMRGCAuk
4 years ago
Interference From High-Dose Biotin Intake in Immunoassays for Potentially Time-Critical Analytes by Roche
Results.— All tested immunoassays, with the exception of toxoplasma
immunoglobulin
M and toxoplasma
immunoglobulin
G, suffered from significant biotin interference.
Results.— All tested immunoassays, with the exception of toxoplasma
immunoglobulin
M and toxoplasma
immunoglobulin
G, suffered from significant biotin interference.
helvella
Thyroid UK
in
Thyroid UK
4 years ago
A little confused and worried.... any advice appreciated
So last month I attended my rheumatology appointment for my fibromyalgia, at my appointment the dr suspected I might have Lupus and sent me off for lots of tests. Everything come back normal apart from Igm levels which were very low, so my immune system is not what it should be. Now because I haven’t
So last month I attended my rheumatology appointment for my fibromyalgia, at my appointment the dr suspected I might have Lupus and sent me off for lots of tests. Everything come back normal apart from Igm levels which were very low, so my immune system is not what it should be. Now because I haven’t
Justmesarah-
in
LUPUS UK
4 years ago
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Are Lung Clinics Secretly Doing Coronavirus Test On Out Patients
I went to lung clinic and over last year doctors not really been intrested even asked about antibody test YET checked nothing BUT this year go and I knew as going during coronavirus Outbreak they would probably do blood test. Not sure of what they look at SO just to be extra I was going to tell em
I went to lung clinic and over last year doctors not really been intrested even asked about antibody test YET checked nothing BUT this year go and I knew as going during coronavirus Outbreak they would probably do blood test. Not sure of what they look at SO just to be extra I was going to tell em
Hidden
in
Lung Conditions Community Forum
4 years ago
Structure of CD20 in complex with the therapeutic monoclonal antibody rituximab
The picture shown above is a ‘flower-vase’ plot* of the molecular interaction between Rituxan and CD20. The grey ‘vase’ represents a micelle which stabilizes the CD20 dimer in vitro; in vivo, CD20 is embedded in the B cell plasma membrane. The yellow ‘root’ represents the transmembrane domains of the
The picture shown above is a ‘flower-vase’ plot* of the molecular interaction between Rituxan and CD20. The grey ‘vase’ represents a micelle which stabilizes the CD20 dimer in vitro; in vivo, CD20 is embedded in the B cell plasma membrane. The yellow ‘root’ represents the transmembrane domains of the
gardening-girl
in
CLL Support
4 years ago
Am I in the clear?
Hi I recently visited my rheumatologist for fibromyalgia and while I was with him he noticed my red rash on my cheeks that I’ve literally had years. He sent me off for blood tests to check for lupus, everything come back normal apart from low Igm levels. Pic attached of my said rash does it look like
Hi I recently visited my rheumatologist for fibromyalgia and while I was with him he noticed my red rash on my cheeks that I’ve literally had years. He sent me off for blood tests to check for lupus, everything come back normal apart from low Igm levels. Pic attached of my said rash does it look like
Justmesarah-
in
LUPUS UK
4 years ago
Newly diagnosed just before Christmas
Due to another condition, I have monthly
immunoglobulin
IV infusions, periodic courses of steroids - this combination seems to have flipped me into diabetes. I started to have very blurry vision 2 days after finishing last course of steroids.
Due to another condition, I have monthly
immunoglobulin
IV infusions, periodic courses of steroids - this combination seems to have flipped me into diabetes. I started to have very blurry vision 2 days after finishing last course of steroids.
Sepsur
in
Diabetes Research & Wellness Foundation
4 years ago
Diagnosis
Hi I recently visited my rheumatologist for fibromyalgia and while I was with him he noticed my red rash on my cheeks that I’ve literally had years. He sent me off for blood tests to check for lupus, everything come back normal apart from low Igm levels. Does this mean I’m in the clear? I do have some
Hi I recently visited my rheumatologist for fibromyalgia and while I was with him he noticed my red rash on my cheeks that I’ve literally had years. He sent me off for blood tests to check for lupus, everything come back normal apart from low Igm levels. Does this mean I’m in the clear? I do have some
Justmesarah-
in
LUPUS UK
4 years ago
My son suffering with chronic itp
Hi, My son at 20months old he diagnosed ITP in 2011,treated with ivig, prednisolone, 2011 to 2013 we suffered a lot...2014 onward he is fine,upto 2020 jan he is fine,one morning he suffering with motions and low fever,That day onwards his platelets counts decreased to 40k...Still we r facing problem
Hi, My son at 20months old he diagnosed ITP in 2011,treated with ivig, prednisolone, 2011 to 2013 we suffered a lot...2014 onward he is fine,upto 2020 jan he is fine,one morning he suffering with motions and low fever,That day onwards his platelets counts decreased to 40k...Still we r facing problem
prasadyarra
in
ITP Support Association
4 years ago
March 7 2020 CLL PATIENT AND CAREGIVER EDUCATIONAL FORUM Saturday 8:00am - 12:30pm Rockefeller Auditorium 430 East 67th St Manhattan
To register: https://newyork2020.questionpro.com CLL Society Inc. • P. O. Box 1390 • Claremont CA 91711 • https://cllsociety.org 2019-2020 CLL PATIENT AND CAREGIVER EDUCATIONAL FORUM In partnership with Memorial Sloan Kettering Cancer Center, the CLL Society invites you to attend our informational CLL
To register: https://newyork2020.questionpro.com CLL Society Inc. • P. O. Box 1390 • Claremont CA 91711 • https://cllsociety.org 2019-2020 CLL PATIENT AND CAREGIVER EDUCATIONAL FORUM In partnership with Memorial Sloan Kettering Cancer Center, the CLL Society invites you to attend our informational CLL
lankisterguy
Volunteer
in
CLL Support
4 years ago
Wondering if I have kidney disease????
My right hand swells, hurts my lower back does even more I'm always tired, headaches Seeing a rheumatologist,cardiologist, and now a hemotologist Took blood test Persistent wbc Crp,high absolute neutrophils, high
immunoglobulin
a 24 hour urine Abnormal protein/creatinine ratio Abnormal total protien
My right hand swells, hurts my lower back does even more I'm always tired, headaches Seeing a rheumatologist,cardiologist, and now a hemotologist Took blood test Persistent wbc Crp,high absolute neutrophils, high
immunoglobulin
a 24 hour urine Abnormal protein/creatinine ratio Abnormal total protien
Andrea1189
in
Kidney Disease
5 years ago
Thyroid blood results querie
Hello everyone I would really appreciate thoughts on my blood results. My current symptoms are muscle and bo e aches, cognitive impairment and fatigue.My liver enzymes are high but liver scans are fine. Do you think there could be a link with these levels and hypothyroidism? I take 125 thyroxin daily
Hello everyone I would really appreciate thoughts on my blood results. My current symptoms are muscle and bo e aches, cognitive impairment and fatigue.My liver enzymes are high but liver scans are fine. Do you think there could be a link with these levels and hypothyroidism? I take 125 thyroxin daily
smilingjane
in
Thyroid UK
4 years ago
Newly diagnosed after years of problems
Hi, everyone. I wanted to take a moment to introduce myself and share my story. I was diagnosed with FND just a few months ago after years of neurological problems. They first started in 2006 with pain, mostly in my back, then I started having bladder problems, a foot drop on the right, mild muscle
Hi, everyone. I wanted to take a moment to introduce myself and share my story. I was diagnosed with FND just a few months ago after years of neurological problems. They first started in 2006 with pain, mostly in my back, then I started having bladder problems, a foot drop on the right, mild muscle
poppymom23
in
Functional Neurological Disorder - FND Hope
4 years ago
IVIG infusion in Mexico
Trying to find out if you can get IVIG infusion therapy done in Mexico and the cost?
Trying to find out if you can get IVIG infusion therapy done in Mexico and the cost?
pragnar
in
CLL Support
4 years ago
Hughes Syndrome - December 2019
The current debate is whether adding in plasma exchange, or intravenous
immunoglobulin
is the better option.
The current debate is whether adding in plasma exchange, or intravenous
immunoglobulin
is the better option.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
5 years ago
I was diagnosed 8 years ago today
I was diagnosed 8 years ago today, as a matter of fact, and I completed my sixth phase of therapy a few weeks ago when I had to get off of Acalabrutinib because of the cardiac effects i was having, which had actually started in my seventh month of Ibrutinib. My previous treatments were Rituxan, in
I was diagnosed 8 years ago today, as a matter of fact, and I completed my sixth phase of therapy a few weeks ago when I had to get off of Acalabrutinib because of the cardiac effects i was having, which had actually started in my seventh month of Ibrutinib. My previous treatments were Rituxan, in
KevinCLLITP
in
CLL Support
4 years ago
Immunoglobulin therapy
Has anyone tried
immunoglobulin
therapy?
Has anyone tried
immunoglobulin
therapy?
JHardiman
in
Behçet's UK
5 years ago
Have you had IVIG treatment for immune issues?
Hello, I have slightly raised NK cells and the best treatment to manage this is IVIG based on analysis of this, intralipids and prednisone. Annoyingly it’s the most expensive treatment and comes with added risks as a human blood product. Please can you get in touch if you have had IVIG treatment? I am
Hello, I have slightly raised NK cells and the best treatment to manage this is IVIG based on analysis of this, intralipids and prednisone. Annoyingly it’s the most expensive treatment and comes with added risks as a human blood product. Please can you get in touch if you have had IVIG treatment? I am
Mogwai_2
in
Fertility Network UK
4 years ago
Are there different IgG formulations for IVIG ?
I thought I read a year or so ago that there may be different formulations of IgG; some better and some not as good. Would someone confirm whether this thought is correct or not and if true, what manufactures are involved. I also understand that there are regional shortages of IgG for transfusions.
I thought I read a year or so ago that there may be different formulations of IgG; some better and some not as good. Would someone confirm whether this thought is correct or not and if true, what manufactures are involved. I also understand that there are regional shortages of IgG for transfusions.
markjeep51
in
CLL Support
4 years ago
GPA flare sinus pain
As the GPA took so much treatment with cyclophosphamide and rituximab to get under control the first time around, my IGG is so low that I will now need to go on
immunoglobulin
replacement.
As the GPA took so much treatment with cyclophosphamide and rituximab to get under control the first time around, my IGG is so low that I will now need to go on
immunoglobulin
replacement.
nicholson27
in
Vasculitis UK
5 years ago
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