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About Me
Doc2B
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About Me
I'm currently trying to set up a way for Australian IVIG receivers to do their infusions at home.
I'm currently trying to set up a way for Australian IVIG receivers to do their infusions at home.
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You reached out with a hug when I first joined, but I have not been checking messages recently. I just wanted to send one back and let you know that it was appreciated.
Good Luck
Thanks for the info,young one, I'm glad you feel it's not REALLY necessary that I have one. I had no idea the port would be in the chest and that solves my problem because Pulm.Doc says no surgery.. Blessings, Penny
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Hug
thanks. Doc i found your discussion about a port and got all the info I need. I've decided not to do it. I get an IV every six weeks and the nurses at the center don't have a problem with it so it just ins"t worth it. Thanks so much. Hang in there. Blessings, Penny
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High Five
good to hear such good news from you. I hope you do well with your exams etc, Tell me about this port when you have the time. I was in the hosp. about a month ago too and a DR.sugessted I have a port inserted. I only get an IV every six weeks and I wonder if it's worth it. Take care and good luck to you. Blessings. janeinva
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Hug
Hi Docy, How are you ? I've been thinking about you and would love to hear from you. take care and enjjoy the holidays, Love, jane
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Support Groups
Close Common Variable Immunodeficiency
I was diagnosed about 1 1/2 years ago, with CVID. IVIG has helped a small it, but mostly my specialist and I are disappointed with the result. Now I'm trying to make it possible for Aussies receiving IVIG to do their infusions at home.
Treatments
- IVIG Somewhat Helpful
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