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shielding letter at last
I suffer from Rituximab induced Hypogammaglobulinaemia so require
immunoglobulin
therapy weekly to maintain my immune system. Will need to be sure life outside is safe before I venture out into the world again. Wishing everyone well. Keep safe. Pam X
I suffer from Rituximab induced Hypogammaglobulinaemia so require
immunoglobulin
therapy weekly to maintain my immune system. Will need to be sure life outside is safe before I venture out into the world again. Wishing everyone well. Keep safe. Pam X
Pam-51
in
NRAS
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
IGa levels
Had a blood test including testing for
immunoglobulin
. First time I've seen IG results so don't understand them as much as WBC etc. My IGa result is in red and is 0.84. I believe the normal range is from 1.0 Those of you that have IVg treatment.
Had a blood test including testing for
immunoglobulin
. First time I've seen IG results so don't understand them as much as WBC etc. My IGa result is in red and is 0.84. I believe the normal range is from 1.0 Those of you that have IVg treatment.
aloneifly
in
CLL Support
4 years ago
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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
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
30 Israeli medical innovations to fight coronavirus
Kamada is developing a polyclonal
immunoglobulin
treatment for severely ill COVID-19 patients, using purified blood and plasma samples from recovered patients. Kamada previously developed serums for treating rabies and Zika.
Kamada is developing a polyclonal
immunoglobulin
treatment for severely ill COVID-19 patients, using purified blood and plasma samples from recovered patients. Kamada previously developed serums for treating rabies and Zika.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
How AHT applies to PD
An increase of 2.6 to 89% in
immunoglobulin
A was observed in nine patients, and an increase of 2.7 to 88.2% in
immunoglobulin
E in eight individuals.
An increase of 2.6 to 89% in
immunoglobulin
A was observed in nine patients, and an increase of 2.7 to 88.2% in
immunoglobulin
E in eight individuals.
kaypeeoh
in
Cure Parkinson's
4 years ago
Coronavirus
Any idea how long it takes for
Immunoglobulin
to get to normal level? Also does PMR itself make us more prone to catching Coronavirus? I am 63 don’t mind self isolating for a couple of weeks but months would be horrendous !
Any idea how long it takes for
Immunoglobulin
to get to normal level? Also does PMR itself make us more prone to catching Coronavirus? I am 63 don’t mind self isolating for a couple of weeks but months would be horrendous !
Breconblue
in
PMRGCAuk
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
COVID-19 pandemic, the Global Rheumatology Alliance
Clinical trials of potential treatments for COVID-19, including antimalarials, tocilizumab, Janus kinase inhibitors, IL-1 inhibitors, IL-6 inhibitors, intravenous
immunoglobulin
and leflunomide, are progressing.
REFERENCE
Philip C. Robinson, Jinoos Yazdany.
Clinical trials of potential treatments for COVID-19, including antimalarials, tocilizumab, Janus kinase inhibitors, IL-1 inhibitors, IL-6 inhibitors, intravenous
immunoglobulin
and leflunomide, are progressing.
REFERENCE
Philip C. Robinson, Jinoos Yazdany.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
Coronavirus - very worried
I now require
immunoglobulin
infusions weekly to maintain my immune system. Have been careful over the last month or so but am now going into purdah as I am in a very high risk group. Please be careful all you people who are at risk until things become clearer. Best wishes. Pam
I now require
immunoglobulin
infusions weekly to maintain my immune system. Have been careful over the last month or so but am now going into purdah as I am in a very high risk group. Please be careful all you people who are at risk until things become clearer. Best wishes. Pam
Pam-51
in
NRAS
4 years ago
Sudden loss of smell as a possible symptom of COVID-19, coagulopathy and antiphospholipid antibodies in patients with COVID-19
Of the patients, 90.6% received antibiotics, 91.8% received an antiviral, 76.5% received glucocorticoids, 44.7% received intravenous
immunoglobulin
, and 38.8% received interferon α2b.
Of the patients, 90.6% received antibiotics, 91.8% received an antiviral, 76.5% received glucocorticoids, 44.7% received intravenous
immunoglobulin
, and 38.8% received interferon α2b.
lupus-support1
Administrator
in
Hughes Syndrome APS Forum
4 years ago
Sudden loss of smell as a possible symptom of COVID-19, coagulopathy and antiphospholipid antibodies in patients with COVID-19
Of the patients, 90.6% received antibiotics, 91.8% received an antiviral, 76.5% received glucocorticoids, 44.7% received intravenous
immunoglobulin
, and 38.8% received interferon α2b.
Of the patients, 90.6% received antibiotics, 91.8% received an antiviral, 76.5% received glucocorticoids, 44.7% received intravenous
immunoglobulin
, and 38.8% received interferon α2b.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
Could I ask for a little support? Today is the day I have the 5th miscarriage.
Hello Everyone, I came across this forum with a broken heart. I was diagnosed APS (single positive) 5 years after my DVT+non-fatal PE and 4 miscarriages. This is quite sad because I am actually a medical personal and always suspected myself to have this condition. My hematologist did not suspect APS
Hello Everyone, I came across this forum with a broken heart. I was diagnosed APS (single positive) 5 years after my DVT+non-fatal PE and 4 miscarriages. This is quite sad because I am actually a medical personal and always suspected myself to have this condition. My hematologist did not suspect APS
Stillsomehopes
in
Hughes Syndrome APS Forum
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
If you want to learn about CLL text or video
Subcutaneous infusions have the advantages of less side effects and better maintenance of your
immunoglobulin
protective levels.
Subcutaneous infusions have the advantages of less side effects and better maintenance of your
immunoglobulin
protective levels.
lankisterguy
Volunteer
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
Discontinue IVIG?
When we started IVF treatment this time around, killer cell blood tests showed that my TNF alpha was slightly elevated so Intravenous Immunoglobin (IVIG) was recommended which I had before FET. We are now 9 weeks pregnant & the clinic are saying I need another IVIG but it was so expensive last time we
When we started IVF treatment this time around, killer cell blood tests showed that my TNF alpha was slightly elevated so Intravenous Immunoglobin (IVIG) was recommended which I had before FET. We are now 9 weeks pregnant & the clinic are saying I need another IVIG but it was so expensive last time we
CW9915
in
Fertility Network UK
4 years ago
Open Heart Surgery W/ ITP
On 11/8/2019 I had my 1st Heart Attack. Platelet Count was 3K. Stents would not be a option, because of lifetime Blood thinners. Would need open Heart surgery - 3 way bypass. This is not possible until my platelets get to 100K to perform the operation. Starting in late Dec 2019 I would start NPLATE injections
On 11/8/2019 I had my 1st Heart Attack. Platelet Count was 3K. Stents would not be a option, because of lifetime Blood thinners. Would need open Heart surgery - 3 way bypass. This is not possible until my platelets get to 100K to perform the operation. Starting in late Dec 2019 I would start NPLATE injections
Dahle2424
in
ITP Support Association
4 years ago
Post 642 I have been scared 8 May 2020
G’day family. Today is VE day, so of course thank you to all that have served. VE day is Victory in Europe When the National SocialistsGerman Working Mens Party (NAZI’s) surrendered in Europe in World War 2 in case “YOU” did not know. In a few months, the Japanese will surrender as well, but it
G’day family. Today is VE day, so of course thank you to all that have served. VE day is Victory in Europe When the National SocialistsGerman Working Mens Party (NAZI’s) surrendered in Europe in World War 2 in case “YOU” did not know. In a few months, the Japanese will surrender as well, but it
RoyceNewton
in
My MSAA Community
4 years ago
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