Calling all caregivers! Join us TONIGHT at 8:00 PM ET for our FREE virtual support group with Eugenie Hsu! Date: 10/14/2025 Time:8pm ET Location: Zoom Register here before 2pm EST zurl.co/QwJli Email [email protected] for questions or additional info.

We're 1 month away from our Pituitary Brain Tumor Family Conference and it is almost sold out! Register now before it’s too late. Join us this year and be part of a growing, empowered community zurl.co/U6rgm

Thank you Lindsay @If You Had Wings, Inc. for the beautiful birdhouse! If You Had Wings, Inc builds custom birdhouses, with all proceeds going to support non-profit groups. Since its launch in 2020, they have donated over $40K to other non profits! zurl.co/CZpFh

Getting to know Mike Brown, one of our dancers for next week's @DCs Dancing Stars Gala ! Mike is dancing in honor of his great-niece Maddie, who has bravely faced a rare brain tumor at just three years old. 👉 Vote with your donation now! zurl.co/hh4oo

Join us for our monthly gathering of strength, support, and shared experiences. This Saturday, our Survivor Support Group is coming together to connect and support one another. 🗓 When: Today ⏰ Time: 3:00pm ET 📍 Where: Zoom Register here: zurl.co/67rPJ

Getting to know Mike Brown before this week's @dcsdancingstarsgala Mike is supporting us in honor of his great-niece Maddie. In this episode, he shares what he is most excited and nervous about for the upcoming event Vote with your donation! zurl.co/AK3DZ

Our Teen Support Group Meets Tonight! We’re thrilled to continue building a safe and welcoming space for preteen and teen hypothalamic-pituitary brain tumor survivors! 📅 When: Tonight! ⏰ Time: 7:00 PM ET 📍 Where: Zoom Register here for free: zurl.co/2w7Ac

Sponsor Spotlight: Silver Sponsor Eton Pharmaceuticals and Bronze Sponsor Everyday Life Foundation! We’re honored to have Eton Pharmaceuticals as our Silver Sponsor and Everyday Life Foundation as our Bronze Sponsor for the 2025 Pituitary Brain Tumor Family Conference!

The next episode of getting to know Mike Brown, one of our dancers for next week's @dcsdancingstarsgala In this episode, he shares what he wants everyone to know about our mission 👉 Vote with your donation zurl.co/jKde4 #DCsDancingStars #DonateToVote #BrainTumor

Congratulations to our dancers @Michaelbrown5921 and @adrifonses for their incredible performances in the DC'sDS Gala! To date, the DCs Dancing Stars Gala has raised over $2.1M to support local charities! Until next year 💃🕺 #dcsdancingstars #fundraising

We’re honored to present another one of our distinguished experts! Fran Castellow, MSEd is the President of Operations for the Patient Advocate Foundation. Don’t miss your chance to join our Pituitary Brain Tumor Family Conference! zurl.co/ZF2up

🎃 Halloween can be a tricky time for families managing hypothalamic obesity, but with a little planning, it’s possible to enjoy the festivities! Here are some tips you can try to make the holiday a bit healthier and less stressful!

November at RAWF! We're all hands on deck for our upcoming Pituitary Brain Tumor Family Conference. If you missed the chance to register, stay tuned to our social media profiles for live updates. And please note this month's support groups are cancelled!

The new National Organization for Rare Disorders (NORD) IAMRARE app gives you a more convenient way to stay involved with our Hypothalamic-Pituitary Brain Tumors Patient Registry! Download the app today from the Apple App Store and Google Play!

Our FY2025 Annual Report is available! These reports share the stories, impact numbers, & financial stewardship that make our work possible. Explore our annual report to see how your generosity & collective efforts drive change and improve lives. zurl.co/oCi7R

November is National Caregiver’s Month! 💙 Caregivers show up with compassion, resilience, and love every single day. Let’s take a moment to recognize their impact, share gratitude, and remind them that they deserve care, too.

Caregivers do so much —from managing appointments & medications to juggling travel, work, & family needs. In the process, they often put their own emotions & well-being last. Thank you, caregivers, for all that you do. Learn more about caregiver resources zurl.co/wY9VN

Today is World Diabetes Day! On this day of awareness, let’s continue to educate, advocate, and push for better care and solutions for all. Share your story or tag someone who inspires you in the fight against diabetes. 💪💙 #rawfcommunity #worlddiabetesday

Thank you to everyone who attended our 2025 Pituitary Brain Tumor Family Conference! It was an incredible weekend of community, teamwork, and in-depth discussions from our amazing speakers. Until next time!

The Credit for Caring Act could change the game for caregivers and families by granting up to $5,000 in annual tax credits to family members providing unpaid care. If you want to show your support for this bill, contact your local representative! zurl.co/GkXaA