The #National Scoliosis Foundation is building a new website to mark our 40th year of service to the #scoliosis community. And, we’d love to have your input!

For four decades we have generated scoliosis awareness, provided patient education/support/communication, trained screeners, facilitated/funded research (cause, prevention & cure), and advocated for early detection and treatment to minimize the physical, emotional and financial burdens affecting patients, and families, living with abnormal curvatures of the #spine.

Your input to our site design effort is important and appreciated. What do you suggest we include on our new website? What information or resources would you like to see to better help you, your family, the greater scoliosis community and/or our mission? What should we add to ease the scoliosis patient journey and improve the quality of life for all?

We are planning some exciting new features, but we value your thoughts and are eager to listen to your needs. No idea is too big or too small. Please email your input to nsf@scoliosis.org.

Thank you in advance for your help!

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