Search
Search
About
Log in
Join
Experiences with
Immunoglobulin M test
Posts
Communities
1,256 public posts
Filter results
First thyroid results (and others are in)
Saw an endo last Friday and got the following results: TSH - 9.91 Thyroglobulin Antibodies - 38.5 Thyroid peroxidase - 9.14 T3 (TT3) - 1.6 Free thyroxine - 15.7 Also these were out of normal range... Bilirubin - 24 Albumin - 53 Coeliac Immunoglobulin IgA - 5.32 I'd be interested in anyone with long-term
Saw an endo last Friday and got the following results: TSH - 9.91 Thyroglobulin Antibodies - 38.5 Thyroid peroxidase - 9.14 T3 (TT3) - 1.6 Free thyroxine - 15.7 Also these were out of normal range... Bilirubin - 24 Albumin - 53 Coeliac Immunoglobulin IgA - 5.32 I'd be interested in anyone with long-term
Hidden
in
Thyroid UK
4 years ago
Immunoglobulin replacement therapy
Hi everyone, hope you are all well. The treatments for my GPA have now beaten my immunoglobulin levels down so low that the Vasculitis clinic at Addenbrookes referred me to the Immunology clinic. They gave me various vaccines and tested my responses and as I didn’t show hardly any response they decided
Hi everyone, hope you are all well. The treatments for my GPA have now beaten my immunoglobulin levels down so low that the Vasculitis clinic at Addenbrookes referred me to the Immunology clinic. They gave me various vaccines and tested my responses and as I didn’t show hardly any response they decided
nicholson27
in
Vasculitis UK
4 years ago
Sweat smells like ammonia
Hello to my fellow lupies! An update on neuro stuff.... still waiting to get IVIG set up. Have not been able to get in touch with neurologist since appt about 3 weeks ago. Rheum won’t write for it. Getting very frustrated and depressed by this whole situation. I keep physically declining. My vision
Hello to my fellow lupies! An update on neuro stuff.... still waiting to get IVIG set up. Have not been able to get in touch with neurologist since appt about 3 weeks ago. Rheum won’t write for it. Getting very frustrated and depressed by this whole situation. I keep physically declining. My vision
Jmiller623
in
LUPUS UK
4 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
T4 Again or with T3?
Here are my results from a week ago: TSH 0.010 -Low – ref. range-0.450 UIU/mL Thyroxine (T4) 7.3 ug/dL - ref. range 4.5 ug/dL – 12.0 ug/dL Triodothyronine (T3) 170 ng/dL – ref. range 71 ng/dl - 180 ng/dL Immunoglobulin G, Qn, Serum – 1054 – 603 mg/dL – 1613 mg/dL My "problem" is this: I'm taking
Here are my results from a week ago: TSH 0.010 -Low – ref. range-0.450 UIU/mL Thyroxine (T4) 7.3 ug/dL - ref. range 4.5 ug/dL – 12.0 ug/dL Triodothyronine (T3) 170 ng/dL – ref. range 71 ng/dl - 180 ng/dL Immunoglobulin G, Qn, Serum – 1054 – 603 mg/dL – 1613 mg/dL My "problem" is this: I'm taking
GKeith
in
Thyroid UK
4 years ago
Reply to Donna re Peripheral Neuropathy
Hi Donna First time posting in this forum . Have read your post and I have experienced similar sensations since March . Neurologist did basic tests and referred me for nerve conduction tests . However these have not happened because of lockdown . She did order a bank of blood tests which I had last
Hi Donna First time posting in this forum . Have read your post and I have experienced similar sensations since March . Neurologist did basic tests and referred me for nerve conduction tests . However these have not happened because of lockdown . She did order a bank of blood tests which I had last
JW2shoes
in
Neuropathy Support
4 years ago
IgM
I’m wondering how many of you have had elevated IgM, and what your dr did to follow up. Mine was elevated July 2019. My internist ran the test and nothing said. My hep knows it was elevated and during my visit with him Friday, he mentioned it but seems he disregarded it. I’m not sure what I think. Seems
I’m wondering how many of you have had elevated IgM, and what your dr did to follow up. Mine was elevated July 2019. My internist ran the test and nothing said. My hep knows it was elevated and during my visit with him Friday, he mentioned it but seems he disregarded it. I’m not sure what I think. Seems
gwillistexas
in
PBC Foundation
4 years ago
Vestibular problems
Hi everyone! Been a long time since I’ve posted. Interesting day today. Saw neuro ophthalmologist today. I have all types of nystagmus. Says it’s probably peripheral vestibular malfunction and maybe something wrong with my ear canals/bones. Wants brain MRI and possible CT angio since I have a small brain
Hi everyone! Been a long time since I’ve posted. Interesting day today. Saw neuro ophthalmologist today. I have all types of nystagmus. Says it’s probably peripheral vestibular malfunction and maybe something wrong with my ear canals/bones. Wants brain MRI and possible CT angio since I have a small brain
Jmiller623
in
LUPUS UK
4 years ago
Has anyone had issues with Hemolytic Anemia?
I am 8 1/2 years into my CLL diagnosis and turned 65 this year, I have had some recent problems with CLL cells appearing in some masses in both my feet and left ankle, but to have a biopsy last week they gave me 4 strong doses of IVIG to support my platelets (i have ITP) as well. I am quite dismayed
I am 8 1/2 years into my CLL diagnosis and turned 65 this year, I have had some recent problems with CLL cells appearing in some masses in both my feet and left ankle, but to have a biopsy last week they gave me 4 strong doses of IVIG to support my platelets (i have ITP) as well. I am quite dismayed
KevinCLLITP
in
CLL Support
4 years ago
Skin Biopsy
Hi, had a punch skin biopsy done on my arm few months ago and it says “direct immunoflourescence shows granular deposition of IgM at the dermo-epidermal junction, together with fibrinogen in occasional dermal vessels”. Says is non diagnostic but suggests connective tissue disease. Just wondering has
Hi, had a punch skin biopsy done on my arm few months ago and it says “direct immunoflourescence shows granular deposition of IgM at the dermo-epidermal junction, together with fibrinogen in occasional dermal vessels”. Says is non diagnostic but suggests connective tissue disease. Just wondering has
Benne09
in
LUPUS UK
4 years ago
Immunoglobulin numbers changing - Flare?
Hi all, A few months ago I got sick. I actually thought it was an infection since some of my more regular flare symptoms were mild or not present for the first two weeks and then I felt better until crashing again. It’s been 2 months of 80/20 awful to “bleh” days. Randomly we decided to test my: IgG
Hi all, A few months ago I got sick. I actually thought it was an infection since some of my more regular flare symptoms were mild or not present for the first two weeks and then I felt better until crashing again. It’s been 2 months of 80/20 awful to “bleh” days. Randomly we decided to test my: IgG
katidid
in
LUPUS UK
4 years ago
Blood test
My last three blood test have flagged up a low igM My Gp has asked my permission to contact Haematology to see if further tests are needed. Has this been a problem with anyone else ? I was diagnosed with PMR September 2019 and currently taking 6mg daily prednisolone
My last three blood test have flagged up a low igM My Gp has asked my permission to contact Haematology to see if further tests are needed. Has this been a problem with anyone else ? I was diagnosed with PMR September 2019 and currently taking 6mg daily prednisolone
Dozzer
in
PMRGCAuk
4 years ago
Doctor Mike Hansen YouTube of may 6th autopsy findings
I saw his previous video had been posted so I thought I would point out this latest you tube. Sorry I do not know how to link on my iPad. He discusses the relationship of APS and CAPS, that infamous cytokines storm. I wondered if there was not some relationship when they were speaking of the antibody
I saw his previous video had been posted so I thought I would point out this latest you tube. Sorry I do not know how to link on my iPad. He discusses the relationship of APS and CAPS, that infamous cytokines storm. I wondered if there was not some relationship when they were speaking of the antibody
christylee
in
Hughes Syndrome APS Forum
4 years ago
ITP and Pregnancy
Hi! I've read through a number of the posts and found them very helpful. I'm 9 weeks pregnant and just found out that my platelet count is at 50. I'm going to see a hematologist and get their expert opinion, but my doctor said she felt that the most likely diagnosis was ITP secondary to an autoimmune
Hi! I've read through a number of the posts and found them very helpful. I'm 9 weeks pregnant and just found out that my platelet count is at 50. I'm going to see a hematologist and get their expert opinion, but my doctor said she felt that the most likely diagnosis was ITP secondary to an autoimmune
FromToronto
in
ITP Support Association
4 years ago
What We Did Right: Israeli Doctors Explain How They Beat the Coronavirus
In the lull following the first infection wave, physicians tell Haaretz how they adjusted on the fly – and helped push Israel's number of new cases per day into the low double-digits 'We’ve also learned that you don’t have to rush into employing invasive ventilation methods. Eventually we began to
In the lull following the first infection wave, physicians tell Haaretz how they adjusted on the fly – and helped push Israel's number of new cases per day into the low double-digits 'We’ve also learned that you don’t have to rush into employing invasive ventilation methods. Eventually we began to
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
Ibrutinib - Joint Pain
I have had CLL for 20 years and have been on Ibrutinib for 3 years. In recent months I have been suffering with aches and pain in the wrists, hand knuckles, knees, ankles and shoulders. I have been treating the symptoms with oral paracetamol and more recently pulse dosing with oral Ibuprofen when symptoms
I have had CLL for 20 years and have been on Ibrutinib for 3 years. In recent months I have been suffering with aches and pain in the wrists, hand knuckles, knees, ankles and shoulders. I have been treating the symptoms with oral paracetamol and more recently pulse dosing with oral Ibuprofen when symptoms
RobertCLL
in
CLL Support
4 years ago
How AHT applies to PD
An increase in
immunoglobulin
M
was observed in nine of the study subjects, ranging from 10 to 28%. An increased Immunoglobulin G was shown in all participants, which ranged from 13 to 36%.
An increase in
immunoglobulin
M
was observed in nine of the study subjects, ranging from 10 to 28%. An increased Immunoglobulin G was shown in all participants, which ranged from 13 to 36%.
kaypeeoh
in
Cure Parkinson's
4 years ago
MUSINGS ON SUBCUTANEOUS IMMUNOGLOBULINS ON A RAINY DAY
Hello on this rainy World Lupus Day, mes amies. I love it when the weather chimes in with my symptoms. I am the rain today. I have had an ongoing roller coaster with respiratory infections since Christmas; every few weeks on antibiotics calms things down, and then up she flares again. All the same, I
Hello on this rainy World Lupus Day, mes amies. I love it when the weather chimes in with my symptoms. I am the rain today. I have had an ongoing roller coaster with respiratory infections since Christmas; every few weeks on antibiotics calms things down, and then up she flares again. All the same, I
lupusinflight
in
LUPUS UK
4 years ago
Thoughts on Covid
Or rather, what I’m watching out for! A vaccine is clearly not a short term solution. It appears likely there will be a vaccine but not a given. Hence world can’t wait in lockdown without destroying economies. Our best hopes for a quick return to the ‘new’ normal are therefore game changing therapeutics
Or rather, what I’m watching out for! A vaccine is clearly not a short term solution. It appears likely there will be a vaccine but not a given. Hence world can’t wait in lockdown without destroying economies. Our best hopes for a quick return to the ‘new’ normal are therefore game changing therapeutics
Paul123456
in
MPN Voice
4 years ago
Lab Report - first sight today
The red figures are: Total bilirubin serum H23
Immunoglobulin
M
L.0.25 WBC 14 (it was 7 in November) Lymphocyte count H9.6 Vit.B12 serum L170 CLL score 4/5 67% disease in all lymphocytes 38% disease in all TNCs If anyone can help to explain I'd be very grateful. Thanks! Martin
The red figures are: Total bilirubin serum H23
Immunoglobulin
M
L.0.25 WBC 14 (it was 7 in November) Lymphocyte count H9.6 Vit.B12 serum L170 CLL score 4/5 67% disease in all lymphocytes 38% disease in all TNCs If anyone can help to explain I'd be very grateful. Thanks! Martin
Alobs
in
CLL Support
4 years ago
30 Israeli medical innovations to fight coronavirus
Whether it’s in diagnostics, treatment or care management, Israel's innovators are busy inventing and adapting technologies to ease the coronavirus burden on the world. By Abigail Klein Leichman MARCH 30, 2020 The coronavirus crisis is first and foremost about people. People stuck at home, people
Whether it’s in diagnostics, treatment or care management, Israel's innovators are busy inventing and adapting technologies to ease the coronavirus burden on the world. By Abigail Klein Leichman MARCH 30, 2020 The coronavirus crisis is first and foremost about people. People stuck at home, people
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
1
...
19
20
21
...
63
Next page
10
20
30
40
50
60
Filter results
Clear filters
Posted in
All communities
CLL Support
319 results
ITP Support Association
154 results
Thyroid UK
133 results
View top 10 communities
Sort by
Most Relevant
Newest