We've built a vibrant community for patients diagnosed with warm Autoimmune Hemolytic Anemia (wAIHA) and their caregivers.
This short webinar will answer all your questions about the wAIHA Warriors Annual Meeting, March 1 - 3 in Nashville. Thank you to our sponsors for making both the meeting and this webinar possible.
wAIHA Warriors produces quarterly webinars and publishes a bi-monthly newsletter. We are also planning our first wAIHA patient conference. Watch for more information.
Through relationships with our industry partners and other rare disease organizations, we share information about the latest clinical trials, advances in research and treatments.
Educating both our state and national lawmakers and engaging federal agencies such as the Dept. of Health and Human Services, CDC and FDA are priorities.
If you would like to work with the Warriors to share your story in the community and in smaller setings, go to our website and sign up to become a wAIHA Champion. This group of volunteers is working on the frontlines to educate and activate friends, neighbors and community leaders in the fight.
The wAIHA Warriors are a 501(c)3 charitable organization, as determined by the IRS, and your contributions are tax-deductible to the fullest extent of the law. Please take this opportunity to make wAIHA Warriors programs and resources available to more patients and care partners.
wAIHA Warriors is a 501(c)3 charitable organization as determined by the IRS. A copy of our determination letter is available on request.
wAIHA Warriors does not provide medical advice or endorse any medication, vitamins or herbs. The information contained herein is not intended nor implied to be a substitute for professional medical advice and is provided for educational purposes only. Always seek the advice of your physician or other qualified healthcare provider before starting any new treatment, discontinuing an existing treatment and to discuss any questions you may have regarding your unique medical condition.
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