MyCP Programs

Congratulations on your !

You are now a member of a diverse community of adults with CP, advocates, caregivers, clinicians, industry professionals, researchers and therapists who have come together to focus on the research that matters most to the CP community. MyCP has three main components:

1. MyCP Forum - people come together here to share lived experiences, seek facts about treatments for CP from professionals, influence our research agenda and to make friends.
2. Participate in research -- right now this is limited to adults and caregivers.
3. Get personalized resources and access to fitness programs.  Please consider recommending these resources to your patients or people you know with CP.

You are now a member of a diverse community of adults with CP, advocates, caregivers, clinicians, industry professionals, researchers and therapists who have come together to focus on the research that matters most to the CP community. MyCP has three main components:

1. MyCP Forum - people come together here to share lived experiences, seek facts about treatments for CP from professionals, influence our research agenda and to make friends.
2. Participate in research -- right now this is limited to adults and caregivers.
3. Get personalized resources and access to fitness programs

Make a difference by taking a survey today.  Start with our informed consent here.

You expressed interest in MENTOR. Please make sure you have reviewed the MENTOR Program page. If you are ready to sign up, please go to the MENTOR Sign Up form.

The Wellbeing Guide is available on MyCP. We hope that the information and quotes in the Wellbeing Guide will give you peace of mind and help you take care of yourself while caring for a loved one with special needs. We have a lot of additional information available on our website including expert videos, web content, book recommendations, external resources and other key programs described below. You can always reach us directly at info@cprn.org.

The Dystonia in CP Toolkit is viewable on MyCP.  You can also explore related information on our dystonia CP pages. We hope the Dystonia in CP Toolkit will provide you valuable information about the diagnosis, treatments, research and experience of living with dystonia in cerebral palsy. We have a lot of additional information available on our website including videos from experts and people with lived experience, web content, book recommendations, external resources and other key programs described below. You can always reach us directly at info@cprn.org.

Webinar Series

We hope you are enjoying our MyCP Webinar Series. Each month we offer a new webinar on our research or interviewing an author from a book on cerebral palsy. You can see and access all of our webinars on the MyCP Webinar Series page or you can subscribe to our YouTube channel.

The CP Toolkit is viewable on MyCP. We hope that the information and quotes in the Toolkit will give you peace of mind and answers many questions about your family's journey with cerebral palsy. We have a lot of additional information available on our website including expert videos, web content, book recommendations, external resources and other key programs described below. You can always reach us directly at info@cprn.org.

The Adult CP Toolkit is viewable on MyCP. If you are not a member or requested the Toolkit to be sent to you, you will receive an email shortly with your access to the toolkit. We hope that the information and quotes in the Toolkit will give you peace of mind and answers many questions about you and/or your family's journey with cerebral palsy. We have a lot of additional information available on our website including expert videos, web content, book recommendations, external resources and other key programs described below. You can always reach us directly at info@cprn.org.

We want to make sure you are aware of our other opportunities get access to expert information, personalized resources and peer support.