Caregiver Corner
Soft Bones is excited to showcase the many caregivers that selflessly help others living with HPP. Because of them, individuals receive the necessary emotional, physical, and psychological support to thrive daily. Whether they are a caregiver by profession or taking care of a loved one, we want to recognize their work and dedication. Nominate a caregiver today!
National Patient Meeting 2023 in Phoenix, Arizona
Nominate a Caregiver
Information is required to contact caregiver.
Caregiver Resources
The Caregiver Action Network (CAN) is a nonprofit organization on a mission to improving the quality of life for those caring for a loved one. They provide resources for family caregivers to help their loved ones and themselves. Check out their tool box and their Rare Disease Caregivers guide.
Caregiver Corner- Darrell K.
What is your relationship to HPP? My wife, Blynda, has hypophosphatasia (HPP). She has two genes and was diagnosed in infancy....
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My connection to HPP is my husband David. I support my husband in his HPP journey. The most rewarding aspect...
Read MoreCaregiver Corner- Ellen K.
My parents and I have one HPP gene. My younger sister has two HPP mutations. With her in a wheelchair...
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