Guest guest Posted February 16, 2006 Report Posted February 16, 2006 " They cant do that, can they? I mean, its done differently, right? family members cant donate or can they? " Valarie - Please don't ever be shy about asking questions. This is how we learn to take extra special care of our pumpkins. = ) IVIg is a blood product (antibodies) -- made from plasma donations. There are plasma donations centers all over the country. Just Google to find. I believe that anyone can donate -- even relatives of a PIDer but there is eligibility criteria (have to be a certain weight, not have certain infections, etc.). The centers will determine whether or not they can use the plasma (a byproduct of blood and blessing in our life). The more people that donate the better chance that your child's (and all of our childrens) particular needs will be met. For example, if only 10 people donated (this was done in the past -- only families would donate) then you would not get a good variety (this is key) of antibodies. Children with Bruton's agammaglobulinemia would die young (~ 30) without the variety of different antibodies that is collected today. If the IgG is the result of 1000 people donating their plasma then there is a better chance that the child might be " covered " with adequate antibodies. A crude analogy would be having a broad spectrum antibiotic (lots of people donating) versus a narrow/selective one (only a few people donating). [As an aside, broad spectrum antibiotics work for some PIDers without IgG/antibody therapy but, for many, this has caused more damage than just starting IgG therapy]. There are some forms of IgG that are selective (e.g., for varicella/chicken pox) and are called, " hyperimmune " products (I think). There are not many of them BUT they do exist for certain types of infections such as RSV. I would encourage anyone that wants, and is able, to donate to do so -- regardless of whether or not they are part of the same family. [As an aside, it is important to know that you can not use family blood for a control sample -- such as when the doc wants (1) your child's blood to test T-cells and a (2) " normal " sample for T-cell function comparison]. Hope that helps. (mom to 4 y.o. who is currently making a mess of bubbles in my home and soaked...running....) osdbmom <osdbmom@...> wrote: In the last week, this has been the topic of conversation around here. The IVIG I mean. Two different family members have asked(offered), if they can donate blood to my kids should they need the IVIG. (which it looks like theywill). They cant do that, can they? I mean, its done differently, right? family members cant donate or can they? I mean, I certainly wouldnt give them any more of my defective genes, most of this mess is " my fault " anyway, but can family members or friends donate to the specific IVIG for your child? and dont laugh, this mess is new to me right now. Valarie with an " A " This forum is open to parents and caregivers of children diagnosed with a Primary Immune Deficiency. Opinions or medical advice stated here are the sole responsibility of the poster and should not be taken as professional advice. To unsubscribe -unsubscribegroups (DOT) To search group archives go to: /messages Quote
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