Board of Directors
Mission Statement
Founded in 1997, the Meningitis Foundation of America is the first national non-profit in the United States of America dedicated to the education, vaccination and eradication of meningitis. Our mission is to support sufferers of meningitis and their families through support groups, advocate for advanced research for the prevention and the long term effects of various meningitis strains as well as facilitating programs to educate the public about the causes and symptoms of meningitis.
Daisi Pollard SepĂșlveda
National President
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Crowned for a cause, international Beauty Queen, model, businesswoman and philanthropist, Daisi Pollard Sepulveda-Low has applied her career of experiences to advocate on behalf of a range of causes. Daisi has embraced the role of an ambassador, spokesperson and mentor for organizations such as Dress for Success, APLA, Minority AIDS Project LA, Salvation Army, Los Angeles Red Cross, and LA’s Prom Closet, among others. She has also worked with professional organizations such as the National Ladies Professional Group and the Asian Professional Exchange influencing and leading numerous of young professionals on ways to pursue their passions and achieve their goals. Daisi P.S. Low has a vast range of studies including leadership, management, international business & marketing, media entertainment, performing arts, along with certifications in fitness, nutrition, etiquette, public speaking and communications.
As the National President of the Meningitis Foundation of America, Daisi takes a personable approach to communicating a message. From fundraisers to community awareness, Daisi’s goal is to personify the organization’s cause by verbally and visually representing the people that the organization supports.
A survivor, Daisi was diagnosed with meningitis during the summer of 2006. Unaware of the severity or long term effects of meningitis, Daisi spent several years overcoming various health and emotional trauma as a result of her struggle with meningitis. “I have learned to embrace my meningitis. I learned how to use it as a tool for self-improvement to make my life better in as many aspects as I can”.
Courtney Martin
National Vice-President
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Courtney has been an instrumental leader when joining the Foundation Board in September 2011. She took the opportunity to represent the Foundation at the annual CoMO meeting in Paris 2011. Courtney has spent the last 4 years as a fundraiser for Meningitis. Her story is as follows:
On October 27th 2007, we were at my middle son’s last soccer game. Ryan was running around playing with soccer balls, eating snacks, drinking his juice, riding on his daddy’s neck, smiling and laughing it was a great day. October 28th it was about 4:30 am Ryan was a little crabby. Ryan was so tired. Ryan pretty much slept throughout the day. I thought he was tired from the big day we had before. I took his temp throughout the day; he had a little bit of one, (he was also teething). On October 29th he was still really tired. I called the doctor, and they said to check for wet diapers and plenty of fluids is what he needs. OK, He didn’t have a wet diaper. He wouldn’t drink anything; I was giving him fluids through a straw. I couldn’t wait the 4 hrs, 6 hrs or whatever, so I went to the ER. We waited for 3 ½ hours before we got to go in. We were probably back in the room for about 2 hrs. They gave him Fluids and got a blood culture, he still wasn’t perking up. On Tuesday, October 30th we got a phone call from the Dr. telling us we need to get him to the hospital. I drove as fast as I could. When we got there they gave him a spinal tap and told us we would be here for about 7-10 days. I was ok with that. We had to wear gloves, mask, and gowns. Poor little guy has got tubes and wires all over him. Around 11:30 p.m. they had put some IV in his leg, it was a blood platelet transfusion I think. That’s when it all happened, nurses started running, and machines were going off, all this beeping, ringing. IT WAS DRIVING ME CRAZY. I was yelling, telling them to help him and screaming. I was going crazy. It felt like a nightmare a very bad dream. On October 31st 12:20 am he was gone. Pneumococcal/streptococcal meningitis just took our son! The ride home was lonely, quiet, and sad. Still in shock. How was I supposed to tell his brothers that he just died? Ryan was such a sweet baby; He is loved and missed every day.
Caroline L. Petrie
National Secretary
Caroline came to the Meningitis Foundation with years administrative and customer service experience. Initially, Caroline undertook the duties of our Web Liaison - this position coordinates all of the various aspects of our website WWW.MUSA.ORG and manages the relationship with our dedicated Web Team in Arizona. In October 2006, she accepted the post of Secretary to the Board of Directors. "Caroline has what it takes to get things organized and get things done." "We couldn't be luckier to have her as part of the team." Caroline makes her home in El Mirage with her husband Doug, a pomarian named Dutchess and Harry her feline companion
Brian Huey
National Treasurer
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Brian was born in Fresno, California in 1972 and lived there until August, 2004. After living in Jacksonville, Florida for just under two years, Brian and family now live in the Houston, Texas area. He and his wife, Susan, have been happily married since 1993 and both very much enjoy their two children. Brian's story is part of this website. Brian became involved with the Meningitis Foundation of America while working on a research project at California State University, Fresno. He picked the topic of Meningitis after having contracted his second incident of the illness a few months earlier. Having attained his Bachelor of Science degree in Information Technology and moved across the country and half-way back, Brian still enjoys the contact with others needing a better understanding of what's going on with the body when Meningitis strikes.
Casey Stewart
National Board Member
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In 1998 at Le Cordon Blue culinary School in Pasadena, CA I was diagnosed with Spinal Meningitis at U.C.L.A., I lost the ability to use my lower extremities and my ability to walk on my own. Michelle and I were married in 2004 and we now live in Palm Desert Ca. I have been working for the last four years at The Silver Rock Resort which is the home of the Bob Hope Classic. I returned to my love of golf with the assistance of a handicapped golf cart called the Solo Rider. Michelle and I wanted to give back so we selected the Meningitis Foundation of America and we now hold an annual tournament at Silver Rock. This will be our third annual tournament and with that try to bring awareness and knowledge to this disease. Michelle and I are truly blessed to have found this foundation and we are very excited about the future of making this Foundation grow. Going all over the country to see different doctors (the Mayo Clinic in Scottsdale, Az. and Mayo Rochester Minnesota) My wish would be to be able to shed some light on how to deal with this illness on an everyday basis and be able to grow from it.
Michelle Stewart
National Board Member
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Michelle Stewart was introduced to the disease of meningitis through her husband, Casey Stewart. Casey is a survivor, and throughout the endless journey of specialists, doctors’ appointments, and living for eighteen months at the Mayo Clinic in Rochester, Minnesota, Michelle discovered the importance of being educated about this disease called meningitis. In order to help understand Casey's symptoms needs, as well as his caretaker, Michelle and Casey took a negative and turned Casey's challenge into a positive by creating 'STEWS SHOOTOUT AT SILVER ROCK.' This is a golf tournament benefiting the Meningitis Foundation of America. Michelle is currently attending Chapman University, studying criminal justice and sociology. Michelle and Casey reside in Palm Desert, California and look forward to many more blessed years raising awareness about meningitis.
Previous Support Staff
- David Spilker, MFA Founder
- Lynn Bozof
- Adam Busuttil
- Jamie Callahan
- James Conway, M.D. - Medical Advisor
- Denise Evans
- Kyle Hendrix
- Sharon Johnson
- Scott Lawson
- Kelly L. Madison
- Tim Milazzo
- Frankie Milley
- Brian Newby
- Carla Newby
- Dayna O'Canna
- Eric O'Canna
- Ryan Pike
- David Powell
- Denise Sanzo
- Kelly Thomas
- Carolyn Waghorn
- Ed Wiginton






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