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rickisjourney's Twitter Updates

Nurse didn't feel like taking an air bubble out so she told me to call her when closer to vein...then she went on break & wouldn't answer 275 days ago
Nuts! After they took the line out of my neck, the tests are back and I need plasmapheresis...like now. 276 days ago
RT @SalixPharma: Join @ALF_USA as they walk for the 30 million Americans affected by #liver disease. The #LosAngeles walk is on 9/18 ht ... 277 days ago
RT @LifeGift: This story is a reason we do what we do at LifeGift! http://t.co/0T7jxCx http://t.co/ayWAwhH 278 days ago
I could hardly sleep last night... You'd think I was starting kindergarten today! Hehe 278 days ago
 

You are not alone - kids with HepC

Posted Apr 22 2011 12:00am
A fellow mom  pointed out this website ( hepatitisc kids ) for kids with HepC. It also has a chat forum for teens battling the disease, which I wish was around when I was younger.
I personally am very interested in hearing how other parents are dealing with having a child with Hep C? Are you doing treatments, or waiting for something better? Do you have a special diet for them, do they take special supplements? Besides keeping my sons diet healthy, giving him vitamins w/ extra C, and really keeping medications away unless completely necessary. (He has to be really miserable or have a pretty high fever to get anything.) I am also waiting a little while on treatments for him. I think in a few more years they will have things fine tuned and may not even have to include interferon. Would love to hear from some other mommas (or dads).

Spread the word! Live Life then Give Life!!
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