BOARD of Directors

My name is Dean Houle and I am the Board President and Chairperson of the Executive and Communications Committees. As President and executive chairperson, I am responsible for the day to day operations of the foundation. As communications chairperson, I am also responsible for all correspondence, social media, website, e-newsletter, public relations and promotional functions of the foundation. 

Throughout my adult life, I've tried to give back to my community. Although I am brand new to the non-profit charitable foundation community, I am not new to volunteering.  I was a volunteer fireman for over twenty years in my local community.  During that time, I was also a medical response technician (MRT) and emergency medical technician (EMT) with the volunteer ambulance for several years. I am also not new to being a board member. I was elected three times to my local town Board of Education and served for a total of twelve years.  This included two years as vice-chairman and two additional years as the board chairman. At the time, our board was responsible for a fifty-million-dollar budget. During my tenure on the board, I chaired or participated on many committees where I devoted many hours outside of regular board meetings. I enjoyed being able to make a difference and giving back to the local community. 

Rare Leader: Dean Houle, President of the Board, Moyamoya Foundation

I was first introduced to the rare disease community in 2014 when my daughter Samantha (the inspiration for the foundation) was diagnosed with moyamoya disease. She was off at college in her sophomore year studying for her final exams when out of the blue she had a stroke. We didn't realize what was occurring initially, but, after a period of several days, we learned that she was experiencing a stroke and would eventually be diagnosed with moyamoya. We were fortunate that the major medical center working with the small rural hospital in her college town knew about moyamoya and she was quickly diagnosed. At the time, there was very little information available about this rare disease. She had to have brain surgery after fully recovering from her stroke. Samantha, my wife Roxanne and I began advocating for young stroke survivor awareness and moyamoya disease with Samantha’s neurologist. We attended Double-A baseball, AHL hockey and stroke awareness events to advocate for awareness.

Then a couple years later it came back even more prevalent. She again experienced strokes and TIA’s and required additional surgeries. Samantha was able to quickly obtain a surgery slot, because another patient’s insurance declined to let them travel for surgery. While she was in the hospital, her cousin Victoria Warren (an event planner) wanted to do something to help us promote awareness of this rare disease that very few had ever heard of.  We originally began discussing creating a large fund-raising event.  By 2018, Victoria had begun creating the Moyamoya Foundation Co. and it was approved 501(c)(3) in Dec 2018.

In January 2020, I joined the Moyamoya Foundation Co. board and was voted in as president. Naturally, giving back to the moyamoya rare disease community which I find myself connected to through my daughter feels right. 

My name is Jill Kennedy and I am the Board Secretary and Co-Head of the Advocacy, Events & Volunteer Committee.  As Secretary, I am responsible for keeping accurate documentation of the board meetings and minutes. As Co-Head of the Advocacy, Events & Volunteer Committee, I handle a great deal of the Foundation’s exposure to the MoyaMoya community and medical professionals.  I have been at the Connecticut Department of Public Health for 26 years.  Currently, I work as a Health Program Associate within the Healthcare Quality and Safety Branch.  This Branch is responsible for the employees that license, investigate healthcare facilities, healthcare practitioners, and the Office of Emergency Medical Services.  My job duties include revising the outdated regulations that govern both healthcare facilities and practitioners and emergency medical services along with special projects for the Branch Chief.

From 2008 to 2019, I was the legislative liaison for the Department.  This consisted of working with the Legislators, Governor’s Office, Office of Policy and Management and sister state agencies to move the Department’s legislative agenda forward during the legislative session.  This position gave me extensive experience on writing a legislative proposal and moving it through the process to change an existing law or enact a new law.  I also sat on and acted as Chair, Co-Chair and Secretary for several different Boards and Committees over years as a representative of the Commissioner, Governor’s Office, and Office of Policy and Management. Lastly, on a part-time basis, I was the recording secretary for the Town of Vernon’s Town Council for 8 years. 

In my personal life, I have extensive experience in being a healthcare advocate for family members.  This includes my parents, sister and late husband.  My dad has been diagnosed with Alzheimer’s and with my mom is getting older, I’ve been working to ensure both of their healthcare needs are being met.  I also have a developmentally disabled sister who is in a group living arrangement.  I participate in all her doctor’s appointments, ensure the entity that handles her finances are doing so appropriately, ensure her needs are being met on a day to day basis and attend meetings with the entity running her program.  I had to advocate for my husband as he went through treatment for cancer twice cancer and a bone marrow transplant.  Ultimately, he passed away in 2011 from complications with the bone marrow transplant.  

I was honored when asked to be a Board Director of the MoyaMoya Foundation and gladly said yes.  My interest had to do with the inspiration of the Board’s creation, Samantha Houle who is like a daughter to me.  I was with her mom the first time she received the phone call where Sam was mistakenly diagnosed with Bell’s palsy.  The next thing I knew I was receiving a phone call that Sam had a stroke.  When Sam was diagnosed with moyamoya, while conducting research about moyamoya, there wasn’t a lot of information on the internet.   I also tried to reach out to hospitals in Connecticut so that her parents could bring her closer, they said that she was in the best place for her recovery.  It was at that time; I knew that advocacy and awareness of this disease needed to begin right away.  I’m hoping that the Foundation can make a small difference in supporting families and patients who must be far away from home and their support systems so the patients can get the best treatment for their disease.  I’m also hoping that the Foundation grow to include members of the medical and patient advocacy community that can help us make a bigger difference in patient’s lives. 

Hello! My name is Lisa Deck, and I am a member of the Board of Directors and co-chair of the Moyamoya Foundation Advocacy, Event and Volunteers Committee.
My purpose is to support, lead and advise the Moyamoya Foundation in its’ mission, programs and goals.  As a member of the MFC Advocacy, Event and Volunteers Committee Co-chair, I share responsibility for all advocacy, event planning and volunteer retention functions of the foundation. 

Outside the Foundation, I am a Founder & Director of Sisters@Heart foundation, a former Go Red for Women National Spokeswomen for the American Heart Association, host and producer of The World of Rare Disease cable show, and an Advocacy Board Member for the American Heart Association in Boston and Southern New England.   I also serve as a Global Ambassador, sharing my personal health experience and patient expertise internationally. Personally, I am a wife and mom of two children and an active volunteer in my children’s schools and activities. 

I am a four time stroke survivor who was diagnosed with Moyamoya Disease after an eighteen year diagnostic odyssey.  It wasn’t until 2015 that I was correctly diagnosed with this rare disease.  I underwent two brain bypass surgery to restore blood flow to my brain.  After the challenging road to recovery, I wanted to help other patients battling this disease.  Personally, I think awareness, advocacy and contributing to research are the best ways to achieve this goal.   When I learned of the Moyamoya Foundation, I knew this was a perfect avenue to help achieve these goals for the Moyamoya Community.  I’m proud to be a part of this organization that selflessly and professionally aims to help others.

My name is Lauren Lindsey I am a Member of the Board of Directors of the Moyamoya Foundation. I have been a nurse for over 14 years and proudly served my community as an ER Nurse in Texas, New York and California. I currently live in Austin, TX and I am a Nurse Clinical Value Analyst for surgery centers in Central and West Texas. I am a mother to an active young boy and we love hiking, nature and wildlife. 

I met my best friend, Beth Mathis, working together as nurses in the ER in Fort Worth, TX. We were always fascinated to find rare diseases and even kept a little notebook to document facts we observed. In 2021 she was diagnosed with Moyamoya Disease, which we never heard of before. One week later we lost Beth due to complications, but her legacy lives on. I believe spreading awareness of this disease is a crucial part of the battle against it. Every year on her birthday we hand out gifts and flyers to spread awareness about Moyamoya through her story. She was beautiful, smart, kind, funny, creative and a loving mother. Her daughter, Mila, was later diagnosed with Moyamoya Disease as well. She has overcome two surgeries at Boston Children’s and is a true Moyamoya warrior. I am honored to represent Beth and Mila through the Moyamoya Foundation to increase research, spread awareness and assist families in need against the battle.