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Neutropenia and PORTLAND!!!???!!!

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Thanks everyone for the responses to my questions about

neutropenia. I feel better. Maggies just had her first ANC done

and it was abnormal. It was done at her first IVIG and I am sure it

will get better now. Molly also had a low ANC before IVIG and it is

now 2200. I just wanted to make sure that I didn't need to worry

about anything else.

I would like to sound off about Portland Oregon. It appears very

strongly that we are moving to Portland in early July. I need to

talk to some other parents/adults CVIDers or PIDer there that can

tell me who is the best immuno....best pediatrician....best place to

live that are resonable (we are willing to go across the Washington

border), best schools...we are looking at Waldorf and also wondering

about Montessori for our 5 year old. I would love to hear from

someone who is in the Portland area. We are very excited as my

family is from there and most of them still live there. Since

moving to Las Vegas, we have not seen anyone in my family for nearly

2 years.

Terri Cerda Mom (46), Molly (5) and Maggie (3) all have B cell

linked CVID.

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