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The Raynaud's Association is considering expanding our organization to local groups serving people with Raynaud’s and would appreciate your input and feedback on the concept.

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* Do you or someone in your family suffer from Raynaud’s phenomenon – an exaggerated response to cold temperatures or stress?

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* Does the idea of a local Raynaud’s group appeal to you?

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* If we did introduce a Raynaud’s group, what would be your primary reason for joining? (please select only one response)

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* If you joined such a group, how would you prefer to meet? (please select only one response)

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* What type of activities would make you more likely to want to attend meetings of such a group? (please check all that apply)

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* What do you like most about the concept of a local Raynaud’s group?

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* What do you like least about the idea of a local Raynaud’s group?

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* Anything else you’d like to share with us or ask us about the concept?

Just a few more questions to help us better understand the opportunity for the concept of local Raynaud’s groups.

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* Is your Raynaud’s the primary or secondary form?

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* Where do you live? Please list City/State or Province/Country

Thanks so much for your input!
If you have experience in working with or managing local self-help groups and would be interested in helping us get new groups started, please share your contact information and previous experience - thank you!

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* Name

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* Where do you live?

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* Previous Experience:

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