Search
Search
About
Log in
Join
Experiences with
Immunoglobulin
Posts
Communities
1,270 public posts
Filter results
Chronic ITP
Hello I have a 5 years old daughter who was diagnosed with ITP at 3 after coming back from a horrible experience at Olympus indoor water park. She came home and had 2 ear infections and was treated with antibiotics, a few days later the rashes came up and her platelets were 3 that's when this nightmare
Hello I have a 5 years old daughter who was diagnosed with ITP at 3 after coming back from a horrible experience at Olympus indoor water park. She came home and had 2 ear infections and was treated with antibiotics, a few days later the rashes came up and her platelets were 3 that's when this nightmare
Kifah90
in
ITP Support Association
7 years ago
igm anticardiolipin antibodies
Hi guys, Finally got app to see GP I spoke to on Tues. Almost had a breakdown on the phone trying to see her as I'm sick of seeing a different one every time and going through all the symptoms...anyway, finally got a referral to see a rhuemy as the above was positive. At least it's a start so one step
Hi guys, Finally got app to see GP I spoke to on Tues. Almost had a breakdown on the phone trying to see her as I'm sick of seeing a different one every time and going through all the symptoms...anyway, finally got a referral to see a rhuemy as the above was positive. At least it's a start so one step
Charliebear68
in
LUPUS UK
7 years ago
NEED MORE ADVICE ABOUT THYROID/CORTISOL LABS
fasting) FREE T3 08/01/2016 3.0 pg/ml 2.0-4.4 pg/ml 09/22/2016 3.5 pg/ml 2.6-4.2 pg/ml 02/13/2017 3.0 pg/ml 2.0-4.4 pg/ml (fasting) REVERSE T3 08/01/2017 15.3 ng/dL 9.2-24.1 02/13/2017 18.5 ng/dL 9.2-24.1 (fasting) THYROID STIMULATING
IMMUNOGLOBULIN
fasting) FREE T3 08/01/2016 3.0 pg/ml 2.0-4.4 pg/ml 09/22/2016 3.5 pg/ml 2.6-4.2 pg/ml 02/13/2017 3.0 pg/ml 2.0-4.4 pg/ml (fasting) REVERSE T3 08/01/2017 15.3 ng/dL 9.2-24.1 02/13/2017 18.5 ng/dL 9.2-24.1 (fasting) THYROID STIMULATING
IMMUNOGLOBULIN
cshepp
in
Thyroid UK
7 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
IVIG
I've been getting IVIG every four weeks since September '16. Since the start on this year I've had one infection after another (upper respitory and sinus) or perhaps it's just one long one that fades then comes back. I've been given two different antibiotics, steroids, mucinex, codine, two different
I've been getting IVIG every four weeks since September '16. Since the start on this year I've had one infection after another (upper respitory and sinus) or perhaps it's just one long one that fades then comes back. I've been given two different antibiotics, steroids, mucinex, codine, two different
johnl
in
CLL Support
7 years ago
Help with bloods and symptoms
My husband has been feeling unwell for several years. Severe fatigue has been the main symptom, along with bad headaches. 18 months ago he started to suffer from tingling in his hands, plus numbness. In time this progressed on to his feet and up his legs and he now has some pain in his heels when walking
My husband has been feeling unwell for several years. Severe fatigue has been the main symptom, along with bad headaches. 18 months ago he started to suffer from tingling in his hands, plus numbness. In time this progressed on to his feet and up his legs and he now has some pain in his heels when walking
Kruzgal
in
Pernicious Anaemia Society
7 years ago
What would you do?
My first post here, although I have been reading and learning for some time. My husband has been feeling unwell for several years. Severe fatigue has been the main symptom, along with bad headaches. 18 months ago he started to suffer from tingling in his hands, plus numbness. In time this progressed
My first post here, although I have been reading and learning for some time. My husband has been feeling unwell for several years. Severe fatigue has been the main symptom, along with bad headaches. 18 months ago he started to suffer from tingling in his hands, plus numbness. In time this progressed
Kruzgal
in
Thyroid UK
7 years ago
Fighting the unknown
I don't know who reads these posts but I am grateful and thankful for any advice. I have mold in my lungs and am on voricanazole. They say I got it by my compromised immune system and CLL. I have lymphoma in my lungs and liver which they say is not related to my leukemia. I will start a regiment of ivig
I don't know who reads these posts but I am grateful and thankful for any advice. I have mold in my lungs and am on voricanazole. They say I got it by my compromised immune system and CLL. I have lymphoma in my lungs and liver which they say is not related to my leukemia. I will start a regiment of ivig
jeepnkaren
in
CLL Support
7 years ago
IgM levels please anyone?
Hi all I very much subscribe to the belief that our blood results don't matter as much as how we're feeling, but I'm curious about something... Most of my results normalised (or nearly) after starting Urso a few years ago, except my Igm. I know that this is quite a sensitive marker but not always included
Hi all I very much subscribe to the belief that our blood results don't matter as much as how we're feeling, but I'm curious about something... Most of my results normalised (or nearly) after starting Urso a few years ago, except my Igm. I know that this is quite a sensitive marker but not always included
Skypony
in
PBC Foundation
7 years ago
CLL Treatment - Give your body a rest?
So Friends - an interesting question for long term CLLers. As this form of Cancer will never be the principle cause of our demise - should we consider putting the CLL Treatment Drugs to one side, to deal with the side effects. My CLL journey started when I was diagnosed in 2001 and treated at various
So Friends - an interesting question for long term CLLers. As this form of Cancer will never be the principle cause of our demise - should we consider putting the CLL Treatment Drugs to one side, to deal with the side effects. My CLL journey started when I was diagnosed in 2001 and treated at various
MartyR
in
CLL Support
7 years ago
No diagnosis yet and feeling ill ☹️
Hi everyone, i would appreciate any advice as I'm new to all this and finding it a little scary. I've been unwell for past 2 years with chronic fatigue, weakness to hands and pins and needles to hands and feet, has gradually got worse over the last month with joint aches and severe head and jaw pain.
Hi everyone, i would appreciate any advice as I'm new to all this and finding it a little scary. I've been unwell for past 2 years with chronic fatigue, weakness to hands and pins and needles to hands and feet, has gradually got worse over the last month with joint aches and severe head and jaw pain.
Yvonne3louise82
in
Pernicious Anaemia Society
7 years ago
Immunoglobulin Replacement
Is anyone on here having infusions/injections to replace low immunoglobulins? I've been advised by immunology at derriford hospital that I'm at risk of severe infections and need to start replacement treatment but I've been at the same igg level since 2013 with no problems. I'd like to hear of people's
Is anyone on here having infusions/injections to replace low immunoglobulins? I've been advised by immunology at derriford hospital that I'm at risk of severe infections and need to start replacement treatment but I've been at the same igg level since 2013 with no problems. I'd like to hear of people's
DevonLottie
in
Vasculitis UK
7 years ago
Seeing a consultant
Hello Guys I have recently been through the whole drama of being admitted with v low platelet counts of 4 (two weeks ago) have had
immunoglobulin
- my levels have gone up to 36 as of last week i have another blood test tomorrow at the hospital but wanted to know how long one has to wait normally to
Hello Guys I have recently been through the whole drama of being admitted with v low platelet counts of 4 (two weeks ago) have had
immunoglobulin
- my levels have gone up to 36 as of last week i have another blood test tomorrow at the hospital but wanted to know how long one has to wait normally to
eveplate
in
ITP Support Association
7 years ago
Post-inactivity muscle pain when walking.
I just have 4-weekly
immunoglobulin
infusions to help support my immune system. I had chemo (FCR) in 2015 and tomorrow my chest infection will be 1 year old - I've baked it a Birthday cake (any excuse).
I just have 4-weekly
immunoglobulin
infusions to help support my immune system. I had chemo (FCR) in 2015 and tomorrow my chest infection will be 1 year old - I've baked it a Birthday cake (any excuse).
snowdroprose
in
CLL Support
7 years ago
IV immunoglobulin Therapy
Does anyone have any experience of IV
Immunoglobulin
Therapy? I keep getting infections that I can't get over and there has been some talk of this Therapy. I've had sinusitis for ten days now .. it's exhausting.
Does anyone have any experience of IV
Immunoglobulin
Therapy? I keep getting infections that I can't get over and there has been some talk of this Therapy. I've had sinusitis for ten days now .. it's exhausting.
Twinkle_12
in
LUPUS UK
7 years ago
Blood results any help would be appreciated
Hi been very unwell for the last 12 months on lots of medication for pain relief, went to the doctors in February 2016 due to a pain in my rib, X Ray done shown multiple collapsed vertebrae and degenatrive wear of lower lumber and also kyphosis, Dextra scan done but doctor said it was ok. I have started
Hi been very unwell for the last 12 months on lots of medication for pain relief, went to the doctors in February 2016 due to a pain in my rib, X Ray done shown multiple collapsed vertebrae and degenatrive wear of lower lumber and also kyphosis, Dextra scan done but doctor said it was ok. I have started
Hidden
in
Pernicious Anaemia Society
7 years ago
Blood results any help would be gratefully appreciated.
Well after 12 months still no diagnosis of Myeloma, several pulomoury nodules of 5mm in my chest, bulky thyroid, lesion on left femur found but they think it is Benign never had injury to Femur, But doctors can not give a reason that I have multiple collapsed vertebrae degenative wear of lower lumbar
Well after 12 months still no diagnosis of Myeloma, several pulomoury nodules of 5mm in my chest, bulky thyroid, lesion on left femur found but they think it is Benign never had injury to Femur, But doctors can not give a reason that I have multiple collapsed vertebrae degenative wear of lower lumbar
Hidden
in
Thyroid UK
7 years ago
Association between thyroid autoimmunity and Helicobacter pylori infection
Immunoglobulin
G (IgG) antibodies to H. pylori were measured as an indication of H. pylori infection. We compared the prevalence of TPO-Ab in subjects with and without H. pylori infection.
Immunoglobulin
G (IgG) antibodies to H. pylori were measured as an indication of H. pylori infection. We compared the prevalence of TPO-Ab in subjects with and without H. pylori infection.
helvella
Thyroid UK
in
Thyroid UK
7 years ago
Vasculitis
Hi I live in Townsville in Australia and have an auto immune condition Vasculitis. I have had Peripheral Vasculitis for two years and have a ride of symptoms and experiences. I went from working a full time hectic job to one day experiencing what they called " dropped foot" to having to stop working
Hi I live in Townsville in Australia and have an auto immune condition Vasculitis. I have had Peripheral Vasculitis for two years and have a ride of symptoms and experiences. I went from working a full time hectic job to one day experiencing what they called " dropped foot" to having to stop working
Vrainbird
in
Vasculitis UK
7 years ago
Please help!
Hello APS family. How is everyone doing? I am very happy to have found this forum, APS is so little recognize and so many people are not aware of it. I need some help and some advice from you guys! About two weeks ago I went to the ER, because of a scotoma on my left eye vision and some zig zag
Hello APS family. How is everyone doing? I am very happy to have found this forum, APS is so little recognize and so many people are not aware of it. I need some help and some advice from you guys! About two weeks ago I went to the ER, because of a scotoma on my left eye vision and some zig zag
Textra88
in
Hughes Syndrome APS Forum
7 years ago
Sad new year 2017
Sadly, my fears have been confirmed...he is now end stage, now needing blood transfusions every 2/3 weeks, this is what's keeping him alive, but Dr expects he will be unable to cope with these constant visits to hospital, hooked up for 7 hours, plus a 4weekly visit for his
immunoglobulin
therapy.
Sadly, my fears have been confirmed...he is now end stage, now needing blood transfusions every 2/3 weeks, this is what's keeping him alive, but Dr expects he will be unable to cope with these constant visits to hospital, hooked up for 7 hours, plus a 4weekly visit for his
immunoglobulin
therapy.
Fightingwithdad
in
CLL Support
7 years ago
1
...
42
43
44
...
64
Next page
10
20
30
40
50
60
Filter results
Clear filters
Posted in
All communities
CLL Support
321 results
ITP Support Association
155 results
Thyroid UK
137 results
View top 10 communities
Sort by
Most Relevant
Newest