Guest guest Posted May 5, 2010 Report Share Posted May 5, 2010 Well tomorrow is the big day, We will start treatment on our 3 year old daughter. To say i'm anxious is an understatement. They told us what to expect but we are still terrified. I have plenty of tylenol ( She's allergic to Motrin) and Benadryl for symptoms. Picked up Pediasure with ice cream for the not eating periods. I know I need to push the fluids hard too. Anything else I should know or be prepared for? I pray to whatever higher power this works. What a terrible disease. I hope we all can defeat this. I take comfort that she has an amazing Doc who specializes in Hep kids. I know other parents who are choosing not to treat due to Genotype vs side effects and rates of SVR. But our Doc feels we have a great chance , she's 6A kindof a rare kind only found in Vietnam, Hong Kong, and Macau. My husband and I cried yesterday when we were remembering while in Vietnam getting her the Doc who did her Visa physical saying to us , " you are good people to take a child who will most likely die of liver Cancer " " Well to him we say HA. We are going to fight this and beat it... And I will gladly take all the years with her than to have faced them never knowing her or taking the chance. Sorry pretty emotional today.. Quote Link to comment Share on other sites More sharing options...
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