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CurePSP

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Support Overview

Another of CurePSP's main goals is to provide those in need with support and hope. We encourage and organize activities that foster face-to-face communication, exchange, and interaction of comfort and mutual benefit to those who are caregivers, family members, friends, and persons with PSP, CBD, MSA and related diseases. These resources and activities include:

  • Support Groups: Online

    Support groups that hold monthly meetings electronically through the use of phone and internet, allowing persons from all over world to participate.

  • Support Groups: In Person

    Support groups that hold monthly face-to-face meetings in locations across the United States and Canada.

  • Peer Supporters

    Volunteers that have personal experience with PSP, CBD, MSA, and related diseases that stand ready to speak with, console, and support the recently diagnosed, and their family, friends, and caregivers.

  • CurePSP Forum

    An online forum that provides an additional avenue for information gathering and dispersion, discussion, and a way for people to share their stories with others.

DISCLAIMER:
The support groups, peer supporters, forum, and support group networks of the Foundation ("Support Group Network") are provided for educational and informational purposes only. This Support Group Network is not a substitute in any way for medical treatment, advice, diagnosis or treatment. Always seek the advice of your physician or other qualified heath provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have learned from the Support Group Network.

The Foundation does not recommend or endorse any specific tests, treatments, physicians, products, procedures, opinions, or other information that may be mentioned at the Support Group Network. Reliance on any information provided by the Foundation, Foundation employees, others in the Support Group Network at the invitation of the Foundation or other visitors to the Support Group Network is solely at your own risk. You should not rely on information you receive from or through the Support Group Network for any personal, medical or health decision, but should consult with a qualified professional for specific information suited to your case.