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The ARPKD/CHF Alliance is solely dedicated to Autosomal Recessive
Polycystic Kidney Disease (ARPKD) and Congenital Hepatic Fibrosis (CHF)
YES WE CAN!
RAISE $100,000 FOR ARPKD/CHF RESEARCH!
The best research is
specific to the disease and should lead to improved patient care.
To Donate Now
New board member Karen Willdermood and her father
Lance
What Karen has to say about the ARPKD/CHF Alliance:
"To say the Alliance
changed my life would be an understatement; the Alliance saved my
life. Through the ARPKD/CHF Alliance, I was connected to doctors at
the National Institute of Health who knew the disease, who could
finally answer my questions. Through the Alliance, I found others
who had similar experiences to mine; I realized I was not alone.
And through the ARPKD/CHF Alliance I found, most importantly,
strength to endure the road ahead.
I am extremely grateful
and excited to be a member of the board. Hopefully, I can give back
to the Alliance what the Alliance has given to me."
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