Guest guest Posted December 31, 2005 Report Share Posted December 31, 2005 from Dale, , welcome to the group. I imagine everyone is doing New Year's stuff with family (or dealing with sick kiddos). So, I'll see what I can do to help you. A great site for you will be to go to the Immune Deficiency Foundation's website at www.primaryimmune.org to start researching what is going on. I'm not real familiar with T-cell problems or " complement " problems -- hopefully, someone with more experience with that end can help you more. I know that if the T-cells are there -- that's good. But they can't be activated if the complement system is defective -- and that's not good. So, I think you are going to have to sit down and ask a LOT of questions of your doctors about what it all means. Most of the time immunologists aren't comfortable talking with the parents until they get entirely through with the testing -- that's aggravating. But again -- every single aspect of the immune system affects a great many different things -- so just one simple tests sometimes makes quite a bit of difference in the prognosis. I do know more about B-cell problems and that is what is involved with not making antibodies to vaccines. One question about her IgG levels -- did they check for IgG subclasses -- they would be listed as IgG1, IgG2, IgG3 and IgG4. Sometimes a person can have a good total count -- but be missing certain subclasses -- leaving them vulnerable to certain infections. Now, if her IgG level is good, but she doesn't make antibodies to vaccines -- then what that usually means is that her IgG is not working (even though the numbers are good). We have a few of those cases in this group. It's aggravating because it doesn't perfectly fit the definition -- but is very real! By re-checking the vaccination levels they will determine whether she was just slow in developing her immune response (maybe they vaccinated her before her immune system was mature enough to produce)or whether she, in fact, doesn't mount a response. So, while the waiting is VERY, VERY hard -- it's absolutely essential to knowing whether or not she needs IVIG and whether IVIG would benefit her. The good news and word of encouragement that I can give you is that my daughter did very well with IVIG. She was diagnosed at 13, started IVIG, started getting healthy for a nice change. Went away to college, lived in the dorm, partied (too much), had her IV's once a month in the dorm room with a visiting home health care nurse, dropped out of college last year to get married and lived happily ever after! (At least we hope that's the way this story ends!) What I want you to celebrate is that because of incredibly fascinating research, doctors these days can offer you a treatment plan that will help your precious little girl -- that would not have been available 20 years ago! It sounds to me like you are dealing with knowledgable doctors. So, the worst part is going to be the waiting and waiting and waiting some more. If they decide to start IV's, that will be something we can all help you get through. This group of Moms have tons of experience and are willing to help! So, when do you expect the results of this latest titer? I'm sure the immunologist is going to be tight-lipped until they come back. Then you need to make an appointment to sit down and discuss everything with him. Let me know if you have further questions. Oh, you can call the Immune Deficiency Foundation office on Tuesday and request their Patient and Family Care Handbook -- it's essential reading -- but I know you want something right now -- so go to their website and look it up. The book is free by just calling their number 1-800-296-4433. Best wishes as you and your family travel through this time of diagnosis. (It really is the hardest part!) And Happy New Year -- getting a diagnosis and a treatment plan will start to give you and your daughter some good days! At least that's my prayer! In His service, Dale Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2006 Report Share Posted January 1, 2006 You can also go to Baxter's Website immunedisease.com and request their newly dignosed kit - it has a CD rom, walks you through everything! Best to you. Dayna Quote Link to comment Share on other sites More sharing options...
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