Changing Patients Lives Every Day
Changing Patients Lives Every Day
BensFriends.org is an international, mission-driven non profit with a network of free, supportive online communities for people affected by rare diseases* and chronic illnesses, as well as their caregivers, family and friends.
Founded by Ben Munoz after a 2006 stroke at age 29, BensFriends.org manages a network of patient-to-patient communities helping tens of thousands of people worldwide through emotional support and connection.
Ben’s Friends is the only organization run by patients, for patients.
*There is no single definition of rare diseases that is accepted worldwide. The United States’ Orphan Drug Act, for instance, defines rare disease as a disease or condition that affects less than one in 200,000 people in the US. For the European Union, a disease is considered rare when it impacts less than 1 in 2,000 individuals.
There are about 7,000 known rare diseases and collectively, about 1 in 10 people (or 30 million people) in the U.S. have a rare disease. Everyone can be affected by a rare disease, directly or indirectly.
|For more information, visit www.bensfriends.org.
Please email us at firstname.lastname@example.org with media inquiries.
512 West MLK #350, Austin, TX 78701
|Download our free, informational brochure here.|
Ben created our first patient community so that he could find someone to connect with while recovering from a stroke.
He and his friend Scott Orn realized what an impact a compassionate community could make in the life of a patient and began creating more patient communities for people with other rare diseases.
Ben was formerly a software developer at eToys and IVT and is a graduate of Stanford University and Kellogg School of Management.
Email Ben at email@example.com.
|50 Ben’s Friends Support Communities|
80,000+ Ben’s Friends Community Members
17,000+ Ben’s Friends Unique Monthly Visitors
7,000+ Rare Diseases
400M+ Rare Disease Patients Around the World
To ensure that everyone in the world with a rare disease has a safe place to go and connect with others like them.
Positively impact our members’ lives everyday.
BensFriends.org is fully supported by donors and corporate partners.. An army of volunteers help out, no one profits, and all donations go directly to funding the networks.
Ben Munoz suffers a serious stroke caused by a rare condition called an AVM.
During recovery he’s alone & unable to find a support group of AVM stroke survivors.
So Ben creates avmsurvivors.org to ensure others don’t suffer alone.
Dozens of people join to find support and friends.
Hundreds more join and express gratitude.
Ben’s classmate and friend Scott Orn helps create the 2nd and 3rd communities and BensFriends.org is formed.
AVMSurvivors.org has 1,000 members.
Ben and Scott launch #4: www.aldsupport.org
New friends join the team to help Ben achieve his mission, launch new communities, raise $.
Blog.bensfriends.org launched with amazing thank you’s, stories, and updates.
BensFriends.org featured in or partnered with Seth Godin’s book Tales of the Revolution, NPR, Extole, Pay It Forward, Brown Alumni Mag, Disability Digest, and more.
BensFriends.org reaches 25 communities & passes 14,000 members.
Partnered with Advocacy for Patients with Chronic Illness (free legal), Friends of Treasure (patient financial assistance), RareDiseaseDay.org (global awareness), 2nd.MD (2nd opinions), Rare Disease UK , Rare Genomics, Patient Power.
Launched mobile app & e-book; featured in TechCrunch, Houston Chron, Harvard BR.
Ben is featured in Forbes Magazine
Receives “LinkedIn for Good and Nonprofit Innovation Grant”
Ben’s Friends was awarded with Yahoo Employee Foundation grant for Project Platform
Ben’s Friends is fully migrated off of Ning and the communities are humming on Discourse
Ben’s Friends launched seven more communities and reached more than 68,000 members and more than 300,000 page views.
Six more patient support communities were launched for people affected by – Raynaud’s Disease, Sarcoidosis, Chronic Pelvic Pain, Epidermolysis Bullosa, Dysautonomia, and Idiopathic Pulmonary Fibrosis.
Ben’s Friends launched an online training facility Ben’s Friends U.
The communities are revamped with a cleaner and simpler look.
Ben is featured in Global Genes
Ben’s Friends is featured in Baylor College of Medicine
|Race car – AVMSurvivors.org member, Michael Hunt, painted his racecar with our logo!||Tattoos – We’ve had at least 2 members get tattoos with one of our logos! How’s that for loving a brand and what we do!?||Fundraising – John Stamler, moderator of ASDSurvivors.org and LivingWithVWD.org, raised over $7,000 for BensFriends.org while running the NYC marathon 6 months after open heart surgery.|
Ben Munoz, President & Co-Founder (firstname.lastname@example.org)
Ben created our first patient community, AVMSurvivors.org, so that he could find someone to connect with while recovering from an AVM-related stroke. Ben and his friend Scott Orn realized what an impact a compassionate community could make in patients’ lives and began creating more patient communities for people with other rare or chronic conditions. Ben was formerly a software developer at eToys and IVT. Ben is a graduate of Stanford University and Kellogg School of Management and was formerly a student of Baylor Medical School. He is also an e-commerce entrepreneur and lives in sunny Austin, TX.
Tom James Lambdin, Co-Executive Director (email@example.com)
Tom James, after a wide and varied career connected to research, medicine and business, looks after the technical and business side of Ben’s Friends. With his background in many aspects of medicine, and his long list of friends and contacts, he is also the Ben’s Friends medical fact checker. He has also long been an active member and moderator of one of Ben’s Friends community. Tom, a rare disease patient himself, lives in the western USA and if he ever had any spare time, he’d be fly fishing.
Clasina Field, Co-Executive Director (firstname.lastname@example.org)
Clasina is a retired Canadian teacher and school counselor who lives near Ottawa, ON. She puts her teaching and counseling skills to good use in managing the Member Experience side of Ben’s Friends. She guides community moderators, deals with members who are having difficulties on the sites, and takes responsibility for the overall experience of Ben’s Friends members. Even prior to becoming a co-ED, Clasina has long been a member, and then also a moderator, of Ben’s Friends. Having a rare disease herself, when she’s not working on Ben’s Friends, Clasina enjoys being home, but she also loves going away and indulging in international travel.
The butterfly is a fitting symbol for our support communities, as it denotes rebirth, transformation and gentleness. Our members often write of having experienced a personal transformation that is truly life-altering, which can reveal new insights about the world and about themselves. Our communities offer a way of helping each other move forward with positivity during the difficult transformation that illness can bring.