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1. Do you have (or know someone) with a diagnosis of hypermobile EDS or a comorbidity?

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2. Are you interested in joining an online Zebra community with access to articles, documents, resources, and products recommended for hEDS?

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3. What form would be most effective for you?

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4. If so, are you willing to invest in development of the benefit?

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5. If so, what amount per month is it worth to you?

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6. Ideas on organizations who can support fundraising efforts?

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7. Other suggestions on raising awareness, sharing resources within the zebra community?

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