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MY OTHER MIND

Fundraising, research, treatment and a community for anyone living with a rare stomach disorder or chronic illness. Become a member or donate today!

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MISSION

It isn't easy for someone with a rare stomach disorder or chronic pain to navigate the healthcare system, the school system, the justice system and more. These systems can get especially hard, and at times dangerous, for low income families of color also navigating systemic racism.

 

We want you to know you are not alone. Don't feel limited by your condition (or your loved one’s condition)– you/ they can still live an amazing life as we work to find cures!​

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We welcome anyone living with or researching Rumination Syndrome, Cyclic Vomiting Syndrome, Gastroparesis and other rare stomach disorders to join the network!​

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MEMBERSHIP

Are you living with a chronic illness or a rare stomach disorder ?

 

Are you the parent/ guardian/loved one of someone with chronic illness or a rare stomach disorder?

 

A Gastroenterologist or health expert studying the gut microbiome & brain connection?

 

An ally or advocate interested in supporting the cause?​

 

Membership includes:

  • My Other Mind Discussion board

  • Online Support group (meetings held virtually)

Join the network

Donate to the cause.

Follow on Instagram.

INITIATIVES

Fundraising + Awareness

Raise awareness in order to fund the treatment and research of the microbiome and gut/brain connection. 

Resources + Care

Build a research and care facility to ensure access to treatment and resources.

Community

Create a platform, build a network and host annual events for teens and adults with rare gut disorders and their families.

CONTACT US

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