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Fibromyalgia Advocacy for Research Funding Continues

Fibromyalgia Advocacy continues as Fibromyalgia Team Leaders head to Washington, D.C.!  Our dedicated group of fibromyalgia advocates set out on new adventures to meet with Congressional leaders in Washington, D.C., to secure increased funding and support for fibromyalgia research, treatment,…

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Fibromyalgia Advocacy in 2024

Join Us in Amplifying Fibromyalgia Advocacy in 2024!  As we step into a new year, our commitment to fibromyalgia advocacy has never been stronger. We are poised to launch the largest grassroots effort yet, working closely with our national Fibromyalgia…

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Fibromyalgia Senator Rally

On May 11th, 2022, Fibromyalgia Delegates successfully met with Congressional leaders on the Hill to share the impact that fibromyalgia had on their everyday lives. Our ask, an appropriations request to open up funding at the National Institute of Neurological…

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Rally for Fibromyalgia Advocacy Day 2022!

  Starting Monday, May 9th through Thursday, May 12th we are asking that you Support Fibromyalgia at Capitol Hill by calling, emailing, and using social media to reach your senators and representatives. On May 11th advocates from around the country…

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Advocacy Day May 11th 2021 – Rally Your State!

Starting Monday, May 10th through Wednesday May 12th we are asking that you Support Fibromyalgia by calling, emailing, and using social media to reach your senators and representatives. On May 11th advocates from around the country will be joining together…

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Candace Lerman, Esq. Interview | Advocacy In Action

Today's special guest is Candace Lerman, Esq.! Candace is an attorney, consultant, and author of the rare disease blog, RareCandace.com We can't wait to learn from all her wisdom! Candace researched and repurposed a drug to put her rare blood…

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Brian Tally Interview | Advocacy In Action

Brian Tally joins us for a special Fibromyalgia Advocacy In Action presentation! He closed a 74-year-old VA legal loophole and changed the law to protect all Veterans. His passion and determination for change is unmatched. Get ready to be inspired!…

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How to submit proclamations | Fibromyalgia & Lupus

We were joined this week with Juana and Estela Mata from Looms For Lupus. They have spent over 10 years advocating for the Lupus and chronic illness community. Part of their advocacy has including proclamations in their local areas. They…

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Rally Your State 2020!

Starting Monday, March 9th through Friday, March 13th we are asking that you Support Fibromyalgia by calling, emailing, and using social media to reach your senators and representatives. We can't allow federal funding for Fibromyalgia to be decreased even more…

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