Immunoglobulin: Hi all, not posted for a while... - Ataxia UK

Ataxia UK

4,141 members4,726 posts

Immunoglobulin

Athywhite profile image
8 Replies

Hi all, not posted for a while, just been 'getting on with it', I had an appointment with my neurologist's team yesterday and she said they are putting me on immunoglobulin in the New Year, probably February as I am only priority 3, the way she explained it seems like there is a possibility I may be able to walk a bit again, has anyone else had this treatment and did it work?

Written by
Athywhite profile image
Athywhite
To view profiles and participate in discussions please or .
Read more about...
8 Replies
wobblybee profile image
wobblybee

🙂I’ve seen posts on Facebook Ataxia Support Groups..It can be variable patient to patient

Athywhite profile image
Athywhite in reply towobblybee

Yes, the nurse told me that, I just wondered if anyone had had any similar treatment and had it worked

Maldrakes profile image
Maldrakes

What will the immunoglobulin do?

wobblybee profile image
wobblybee in reply toMaldrakes

ataxia.org.uk/research-news...

PatsyIpswich profile image
PatsyIpswich

I asked for it but was told not appropriate for me. Good luck anywhere worth a try x

penelope2 profile image
penelope2

Does this mean you have an autoimmune type of ataxia? This means your autoimmune system has gone into disarray, caused by something your eating, in your environment, exacerbated by stress or trauma. Could be any of these or a combination of different factors or perhaps something else?Maybe it's not autoimmune, I do wish the doctors would explain more, we need to understand so we can help ourselves as much as possible.

Forget GPs, they have very little knowledge but can you question the consultants more?

Good luck.

isabelalfaiate profile image
isabelalfaiate

I had immunoglobulin in my thirties (no ataxia symptoms then) because i kept on having bronchitis weekly and antibiotics were no longer effective. I have never had bronchitis since that shot. It may work for you, hope so. best wishes

coat2003 profile image
coat2003

i am allergic as an ataxian.my gp in Slovakia always requested levels as i have eczdema, allergies.am i NOT BLESSED AN ATAXIA ALSO...no, i cannot answer as quite further with ataxia inhereted type sca 2.but it puzzled me...i'd love to hear more. and Wobbly bee is very right.

Not what you're looking for?

You may also like...

Support for my lovely Mum

Hi, My 63 year old Mum had a stroke last year caused by a venous anomaly in her brain (very...
Totoro123 profile image

Daughter with unlabelled ataxia

Hi, I have been a member of this forum for a few weeks and have reading the posts with interest and...
becsjlittle profile image

I am in need of some advice on ATAXIA... Please

My 2 1/2 year daughter was diagnosed at birth with hypoxic ischaemic encephalopathy grade 2 and...
vanessa2012 profile image

info for understanding For Me Jemma 42

Hi everybody, I am new here, I seen my Neurologist Last Thursday, and she said that it is time to...
lottiejemma profile image

My wife's current condition

Following radiotherapy and aggressive chemotherapy to treat Stage 4 Lung Cancer (non-small cell...
DizzyLady profile image

Moderation team

See all
HarryB profile image
HarryBAdministrator
VE93 profile image
VE93Administrator
WendyBom profile image
WendyBomModerator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.