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CVID/IVIG/Eye Problems
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CVID/IVIG/Eye Problems

Does anyone have any information on possible side effects on the eyes when taking IVIG for CVID?
Tags: CVID
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7 Comments Post a Comment
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Avatar_n_tn
I'm sorry I don't have an answer to your question, but I have a question I'm hoping you could answer. I'm looking for a forum to discuss CVID. I was diagnosed when I was 8 years old. I took daily antibiotics for a number of years, but managed to gain some control of it through my teens. I suffer from sinusitis and brochitis several times a year, and have had some strange infections; I've managed it all through tons of antibiotics and lots of time at home resting. However, I'm 29 and things seem to be getting a bit worse. I haven't seen an immunologist since I was a kid, I'm not even sure if I'm sick enough for treatment. Do you know of a forum where I can discuss this? I'd really appreciate any advice.
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Avatar_n_tn
    I have not read anything about IVIG causing problems with the eyes yet IVIG has many possible side effects so it is possible.
   I was diagnosed with low immunoglobins over 20 years ago, and I have suffered with frequent infections since childhood. I started on IVIG in the summer of 2006. Why the delay in treatment? Because over 99% of physicians have little or no understanding of CVID. Most of us who finally receive treatment have been through years of suffering. I am not angry or bitter about this, yet I do find this frustrating. I, too, would love to have a way to communicate with other CVID patients.  Being able to discuss the unique problems we face would benefit all of us. Please let me know if you find any good forums and I wish you both the best.
    
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Avatar_m_tn
Try Ipopi.org or primaryimmune.org
Both are terrific and you'll find most everything you need.
Lyn
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Avatar_n_tn
hello...I was diagnosed with CVID over  10 years ago and have been treated monthly for the past 10 years with 10 grams of Immune gamma globulin.  Now I have recently diagnosed with 2nd stage  lyme disease. Does anybody know whether or not they screen blood products for lyme disease?? I was told that they just ask the donator if they think they might have it. Let me tell you..CVID and LYME together are pretty hard to swallow....

anyone know anything?
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Avatar_n_tn
WELL I HAVE CVID  AND NOW TO FIND OUT I ALSO HAVE LUPUS AND STICKY BLOOD CELLS CALLED ANTIPHOSPHOLIPID ANTIBODY SYNDROME. I RECEIVE IVIG MONTHLY OF CARAMUNE AND THEY HAVE PLACED ME ON CMBALTA FOR THE FIBROMYALGIA.
I ALSO DO EVEN GET A SWEET HELLO FROM MY IMMUNOLOGIST WHEN I GO MONTHLY FOR TREATMENT. HE TOTALLY AVOIDS ME AND IF TO TALK TO ME FOR 10 MINUTES A GET A BILL FOR $225.00. SO I ALSO TOOK IT UPON MYSELF TO SEE A RHEUMATOLOGIST IN WHICH I ADORE. CHECK INTO IT.
I HAVE A MYSPACE PAGE FOR SUFFERERS SUCH AS US. IT IS UNDER      "mychildisalwayssick"       you should go there. i fill it with wonderful info and pics of some of us who suffer. I UPDATE REGULARLY OF THINGS TO WATCH FOR AND SUCH. THIS IS A WONDERFUL SUPPORT GROUP ALSO. GOOD LUCK AND PRAYERS. IF YOU CANNOT FIND THE PAGE SEARCH MY NAME UNDER CONNIE RUSK AND THEN CLICK THE FIRST FRIEND ON MY LIST (THAT WILL BE THE SICK PAGE)
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Avatar_n_tn
Regarding one of the posts someone was asking if eye problems can be related to CVID.  I have chronic uveitis on relapsing remitting optic neuritis.  Since I was diagnosed with CVID and given adequate doses of IVIG, my inlammatory problems in my eyes has improved greatly.  It went from chronically swollen painful eyes despite prednisone drops etc, to no pain whatsoever as long as I continued a small dose of the steroid drops.  This was my experience. Maybe someone else has a comment.
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Avatar_f_tn
Hi,
The Immune Deficiency Foundations has a forum for adults called Friends where you can post questions and discuss what's going on. It's a great support group for all and the Foundation has events all over the USA.  The National Convention will be in June 2013 in Baltimore and is designed for the patient and their families.  Great speakers on what PIDD patients deal with as well as support group meetings.  Lots and lots of fun and loads of information.  check out primaryimmune.org
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