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Board of Directors 

For more information about each Board Member and the project(s) they are involved in please, click on the Board Member's name.


Officers Founders

President
Judy Hunt
Judy_Hunt@ASAP.org 

Vice President
Theo Kotjarapoglus
Theo@ASAP.org 

Secretary
Sara Patterson
Sara_Patterson@ASAP.org

Don and Barbara White

 

Directors at Large

Patrice Schaublin 
Patrice_Schaublin@ASAP.org

Karen Spiroff, R.N.
Karen_Spiroff@ASAP.org

Ellie McCallum
Ellie_McCallum@ASAP.org

Matt Turmelle
Matt_Turmelle@ASAP.org

William Hagelgans
Bill_Hagelgans@ASAP.org

Arnold Menezes, MD

John D. Heiss, MD


Board of Directors - Individual Biographies 
Judy Hunt 
President 

Judy lives in the Minneapolis/St. Paul metro area of Minnesota. She was first diagnosed with syringomyelia in April 1997. 

Judy began serving on the ASAP Board of Directors in 1998. During her seven years of service, she held a variety of positions on the Governance, Development, Marketing, Programs and Conference Committees. She also helped to launch two very successful member programs: Circle of Friends in February 1999, and the bi-monthly publication, ASAP Faces, in June 2002. In September 2002, she was elected Secretary. Judy became President-Elect in November 2003, and President in October 2004. 

With two Bachelor of Science degrees (she graduated magna cum laude), Judy brings her expertise in organization and structure to ASAP. As President, she remains involved with the networking, peer support programs, and various committees. Judys sense of community is strong, and she is deeply committed to ASAP's mission; to improve the lives of persons affected by syringomyelia, Chiari malformation and related disorders while we find the cure. 

Judy has also served for seven years as a Board Member of her local para-transit agency, which works toward achieving better transportation for people with disabilities. She serves on the Board of Directors of her townhouse association, and also manages an online writing community. She enjoys reading, writing, and electronic media. 

Judy relates, I have firsthand experience with the many problems associated with the disorder, ranging from difficulties dealing with doctors to the grieving of our lives as they used to be. Members need to feel connected with ASAP. Only then will they become involved. Then we, as a group, can better confront the challenges that face us." 

 



Theo Kotjarapoglus
Vice President

Theo Kotjarapoglus lives in Boiling Springs, PA, where he is recently retired. He has been active with ASAP during the last year serving on the finance committee and working with development. He has extensive expertise and experience in the non profit community.

Theo said, "A family history of neurological disorders brought me to ASAP. I am very committed to the work of ASAP."

 


Sara Patterson
Secretary

Sara Patterson resides in Palm Bay, Florida with her husband and three children. She learned about ASAP when her daughter, Holly, was diagnosed with syringomyelia in 1996. Since that time Holly has undergone numerous brain and spinal surgeries. Holly was the second member of the family to be diagnosed. Years earlier, Sara's mother had learned the cause of her disabling headaches, neck pain and muscle weakness were due to SM.

For the Patterson's, volunteering is a family affair. Sara and her husband, Stuart, a software engineer, created, designed and managed ASAP's first website in 1997. Periodically over the years, Sara, Stuart and their son, Ryan, have served on ASAP's IT committee.  Not to be left out, Sara's daughters, Hope and Holly, are well-seasoned fundraisers and ASAP ambassadors. They are both members of the ASAP Kids For A Cure Club and have organized many fundraisers to benefit ASAP.

Sara's educational background is Public Administration. She currently works part-time at an inclusive preschool for children with and without special needs. She is actively involved in the nonprofit sector, and is happy to share her knowledge and expertise to help advance ASAP's mission.

This is Sara's second time serving on the ASAP Board of Directors. She completed a three-year term in 2000, and is now serving as ASAP's Secretary.


Karen Spiroff, R.N.
Director-At-Large


Karen Spiroff lives in Richmond, Virginia and is the mother of two girls, Stephanie and Kimberly. She learned about ASAP in 1999 when her youngest daughter was diagnosed with SM and CM. Karen has been an active volunteer for ASAP for many years and both of her daughters are members of ASAP's Kids For A Cure Club.

A registered nurse in the states of Virginia and New York, Karen brings to the board fifteen years experience in home health care, medical-surgical, and peritoneal dialysis. She is currently employed as a telephone triage nurse.

Karen exemplifies the spirit of caring by offering support to newly diagnosed families and those struggling with issues relating to SM/CM. Caring for her daughter has provided on the job training in the areas of adaptive equipment, coping strategies, and alternative methods of pain relief such as acupuncture and massage therapy. She has learned to deal successfully with the school system in order to provide her daughter with necessary modifications and is always willing to share her knowledge with others.

Karen is also a volunteer and strong supporter of Canine Companions for Independence. Her family is the proud caregiver of Lace, a Labrador retriever who provides assistance and companionship for Kimberly.

Karen is excited to be a part of the ASAP Board of Directors and is looking forward to seeing ASAP grow and expand.


Ellie McCallum
Director-At-Large


Ellie McCallum lives in Camas, Washington.  Her husband Jim was diagnosed with syringomyelia in 1949.  At that time the doctors could only give it a name.
 
Jim and Ellie were introduced to ASAP in 1995.  Even after Jim's death, Ellie has remained active in the organization because she feels it is important to give support to those with the disease and to fight for a cure so others will not suffer as Jim did.
 
Ellie has a B.A. in Education and an M.S. in Library Science.  A former school teacher and school librarian for 26 years, Ellie loves to research.  She is an active member of St. John's Presbyterian Church in Camas and volunteers with Friends of the Carpenter, a faith-based organization that works with the homeless, building relationships and assisting those in need. She has four grown children and five grandkids.
 
By sharing her compassion, understanding and support to members, Ellie hopes to encourage others to become more involved with the work of ASAP and the quest to find a cure.  She is strongly committed to ASAP and has a deep sense of urgency to fulfill our mission statement.
 
Ellie's can-do attitude shines through each project she undertakes. "I will try very hard to complete whatever task I am called upon to perform." 

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