Our Board & Staff
Akesha Allen was introduced to the hemophilia community when her son was diagnosed with Von Williebrand Disease. This diagnosis is what propelled her to become more involved in research and treatment options not just for her son, but for ALL people who have been and will be impacted with this disease. Akesha has extreme passion for full and complete inclusion for all communities to be represented within Louisiana Hemophilia Foundation. While holding Board of Director positions with other organizations as well as a participant of the Von Williebrand Therapeutic Policy & Advocacy Advisory Board, Akesha is able to bring an aspect to our community which will allow for greater relationships to be built with underserved communities.
My Name is Subodh Pethe. Most of you probably know me as Ben's dad. I became involved with the bleeding disorders community the day Ben was born with severe Hemophilia. Over the years I have seen the LHF go through some good times and bad. Throughout it all they have always done what they can to help the bleeding disorders community.
I make my living as an IT Pro, what that means is people hire me to fix their problems with technology and related workflows. Now that Ben is in high school, I decided to get actively involved with the LHF. I want to put my experience guided by intelligence to help make LHF the best chapter in the world.
My name is David Reynaud and I would like to take this opportunity to introduce myself as one of your new LA Hemophilia Foundation Board members. I have recently been elected the Board’s secretary.
I am 42-years old and have severe Hemophilia A, which I feel truly qualifies me to serve you as I share a common bond with those with bleeding disorders. Also, by being raised in a “Hemophilia” family, I can relate to family members and I understand the unique challenges that arise while living and caring for someone with a bleeding disorder. Also, I have access to a wealth of knowledge and experience from my Uncle (fellow sever hemophiliac), as well as from my parents, who in the past have been very active in the LHF.
I am married to Nicole Fassbender Reynaud, who many of you already know as she is the nursing coordinator at the Tulane Hemophilia Treatment Center for Bleeding and Clotting Disorders. Nicole and I have been married for nearly 18-years and we have a 7-year old daughter named Watson, a Scottish Terrier named Stewie, 13 chickens, one rabbit and a newly adopted kitten named Gracie.
I enjoy cooking, reading, traveling and I am very passionate about the game of golf. Even with a total knee replacement, a fused ankle and a severely arthritic elbow, I can hold my own on the course. Never hesitate to ask me to play should you need to fill a foursome.
I would like each and every one of you to know I am available anytime should you need to speak or meet with me. We, the Board of Directors, are here to serve you and we welcome your ideas and visions to make LHF the wonderful organization we all know it should be.
Thank you for letting me serve you and please call me is you need anything. I can be reached anytime at 225-623-9287.
Ashley Castello is a mom of two boys, nine-year-old Leo and 3-year-old Max. Max has Severe Hemophilia A with inhibitors. From the moment he was diagnosed, Ashley and her husband Casey knew that they would want to be involved in the community. Ashley joined the board with the hopes of making a positive difference for families affected by bleeding disorders. Ashley is an educator with sixteen years of experience in the East Baton Rouge Parish School System. In her current position as ICARE Specialist, Ashley provides prevention services to five schools in EBR and the adjudicated youth program as a Licensed Prevention Professional. In addition to her job in EBR, and her role as treasurer of the LHF Board of Directors, Ashley has also served on the Advocacy Leadership Council of the Hemophilia Federation of America for the last year and a half. She is dedicated to continuously improving LHF and ensuring that the bleeding disorders community has a reliable chapter for many years to come.
HTC Board Representative
Jennifer Borrillo, MSW, LCSW, MBA has been a clinical social worker for almost 30 years. She has been with the Louisiana Center for Bleeding & Clotting Disorders at Tulane University for the past 17 years. She initially started at the Center as a part-time hemophilia social worker. After Hurricane Katrina devastated New Orleans in 2005, destroying Louisiana’s State Factor Program located within the city, Jennifer helped launch the Center’s 340B factor program which began serving patients in January 2007. Jennifer is currently in her thirteenth year as the Director of 340B pharmacy program and her fifth year as the Administrative Director of the Center. She earned her MBA from the Tulane University Freeman School of Business in 2010, while working full-time, and received an appointment to the clinical faculty of the Tulane School of Medicine, Department of Hematology/Oncology. Jennifer is passionate about working with her Center’s patients and is dedicated to helping them secure the care and resources that they require. In 2013 Jennifer was awarded the Tulane Department of Medicine Chair’s Award for Excellence in Departmental Service and in 2016 the Louisiana Hemophilia Foundation’s Annual Advocacy Award. Previously, Jennifer served as the Great Plains Region NHF Social Work Working Group Representative. Jennifer is the current Board Chair of the Hemophilia Alliance and is on the NHF CCSC Advisory Board. Jennifer and her husband, Dr. Christopher Borrillo, have four children together, and live in New Orleans, Louisiana.
HTC Board Representative