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Fundraise and Promote on Social Media

Fundraise and Promote on Social Media

Fundraise During #VAM26

Peer-2-Peer fundraising is an easy way to raise awareness and make an impact during Vasculitis Awareness Month (#VAM26) and to celebrate our 40th anniversary.

You can easily share your fundraiser with your friends, who can then donate and share with their friends.

Fundraise on Facebook
Fundraise on Givesmart
Graphic from the Vasculitis Foundation promoting Vasculitis Awareness Month in May, featuring the text “Vasculitis Awareness Month” and the message “You Are Not Alone.”

Make Your Own VAM Posts

Check out our downloadable graphics!

Social Media Profile Picture

Vasculitis Awareness Month graphic featuring a red and white patterned awareness ribbon on a purple background with the message “You Are Not Alone.”
Download Profile Picture

Sample Facebook Graphics

Vasculitis Awareness Month graphic with bold text “Your Support Changes Lives” and a link to vasculitisfoundation.com/vam.
Group of Vasculitis Foundation supporters wearing “Victory Over Vasculitis” shirts posing together outdoors, with text reading “Rare does not mean invisible” and a link to VasculitisFoundation.org/VAM.
Illustrated group of diverse people standing together under text reading “We support Vasculitis Awareness Month” and “You Are Not Alone.”
Download Facebook Graphics

Sample Instagram Graphics

Vasculitis Awareness Month graphic defining vasculitis as inflammation of blood vessels that can restrict blood flow and cause organ damage, with pronunciation and link to VasculitisFoundation.org/VAM.
Collage of community members, supporters, and speakers surrounding text reading “May 2026 Vasculitis Awareness Month” and “You Are Not Alone,” with the Vasculitis Foundation logo.
Vasculitis Awareness Month graphic reading “Take Action. Make a Difference.” with four options: make a gift, shop anniversary gear, celebrate community heroes, and start a fundraiser, plus a link to VasculitisFoundation.org/VAM.
Download Instagram Graphics

Help raise awareness. Share our posts. Make an impact.

vasculitisfoundation

2,255

40 years supporting the vasculitis community
Free Resources • Support Groups • Education
⬇️ Show your support + learn more

vasculitisfoundation

View Instagram post by vasculitisfoundation

Nov 1

Open post by vasculitisfoundation with ID 18190519441409372
40 years ago, a vasculitis diagnosis meant facing uncertainty with few answers and limited support. Look how far we’ve come together.Thanks to supporters like YOU, we’ve:🔬 Funded 80+ research studies advancing better treatments🩺 Trained the next generation of vasculitis specialists📚 Helped develop the American College of Rheumatology/VF Treatment Guidelines💙 Built a global community connecting patients and families with trusted education and supportWe’ve accomplished so much in 40 years. But there’s still more to do.Help us shape the next 40 years. See how your gift can make a difference at the link in bio.Special thank you to our annual appeal & awareness sponsor, @amgenbiotech!

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 31

Open post by vasculitisfoundation with ID 17961708297266704
We're wishing everyone a Happy Halloween!Whether you’re dressing up, handing out candy, or enjoying a cozy night in, we hope your day is filled with light-hearted fun and moments of joy.Stay safe and take good care of yourself! You deserve all the treats! 🍬🎃

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 30

Open post by vasculitisfoundation with ID 18130838692856236
Your voice can help shape the future of vasculitis care. Join us for the Vasculitis Community Forum: Patient Perspectives, a national virtual listening session where patients, caregivers, and clinicians share lived experiences with those who make treatment decisions, including regulators at the FDA.📅 Friday, November 20, 2026🕛 12:00 to 2:00 PM ET💻 VirtualThe focus: the urgent need for safer, more effective alternatives to steroids, and the real-world impact of current therapies.Register at the link in our bio.

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 29

Open post by vasculitisfoundation with ID 18114636071613047
Vasculitis can feel isolating, especially when you’re the only person you know who has it. 💜Our support groups are a place to connect with people who truly understand, from the first-diagnosis questions to the tired days and the small wins.Register for free at the link in bio

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 26

Open post by vasculitisfoundation with ID 17927906268426173
And the Dundie Award for “Not Understanding Chronic Illness” goes to… everyone who said it was just stress.It can be frustrating, isolating, and invalidating when symptoms are dismissed instead of investigated. Many people living with vasculitis go through this kind of delayed recognition before finally getting answers.If this resonates with you, you’re not alone and you deserve to be heard.Learn more at the link in bio

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 25

Open post by vasculitisfoundation with ID 18128969576297043
Movement doesn't have to mean a full workout. 💛Parking a little farther from the door. Taking the stairs when you're able. Stretching while you watch TV. These small moments of mindful movement can add up, and for many in our vasculitis community, gentle movement can help support joint mobility, energy levels, and even mood. Of course, always listen to your body and move at your own pace. Every step counts, even the small ones.A huge thank you to Jim Walters for joining us at this year's symposium!

36 1

vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 22

Open post by vasculitisfoundation with ID 18117325483801374
Living with vasculitis often means living with medications, and with the side effects that can come along with them.Some days it’s a routine you’ve mastered. Other days it’s a new challenge you didn’t see coming. Either way, the people who understand it best are the ones walking this road too.Our online Vasculitis Voices chat community on Inspire is the perfect place to ask questions and dive deep into the conversations that matter to you with people who get it. Plus, it’s free to join!Join the conversation at the link in bio

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 20

Open post by vasculitisfoundation with ID 18149878075556832
Your kidneys don't always announce when something's wrongA few things that can point to kidney involvement: blood in your urine, foamy or bubbly urine, swelling in the legs or around the eyes, high blood pressure, fatigue, and a noticeable decrease in urine output.This isn't a diagnosis tool, just something to keep on your radar. If any of these sound familiar, bring them up with your care team.

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 19

Open post by vasculitisfoundation with ID 18384803827225611
Living with vasculitis is a journey, and some days are harder than others. Your strength and energy may come and go, but every day holds victories... big or small.Share you story at the link in bio

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vasculitisfoundation

View Instagram post by vasculitisfoundation

Oct 12

Open post by vasculitisfoundation with ID 18118209547978777
Think vasculitis only happens later in life? Think again. This disease can impact anyone, at any age. Awareness and early recognition are key to getting the right care when it’s needed most. 💙

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Thank you to our 2026 Vasculitis Awareness Month Sponsor:

amgen logo

YOUR GIFT GOES TWICE AS FAR TODAY!

Double Match Day is here—help us celebrate 40 years by raising $40,000.

People living with vasculitis rely on support, research, and connection every day.

Today only, your donation will be matched dollar-for-dollar, helping us reach more patients, fund critical research, and ensure no one faces vasculitis alone.

  • Available Wednesday, May 13, 2026 only.
Double my impact