Today is a very exciting day. I will be on my journey to help so many! I will be meeting with the Epilepsy Foundation of CT., there will so many upcoming and exciting events that I will share with you tomorrow. “The Epilepsy Foundation of Connecticut is a leading source of information, education, recreation and ADVOCACY and support for approximately 60,000 people in Connecticut who have epilepsy. The organization meets all of the standards set by the National Epilepsy Foundation and is Connecticut’s only state affiliate. They maintain a diversified funding base with revenue derived from individual and corporate contributions, private foundations and a variety of fundraising events.” So, Please stay tuned for wonderful upcoming information just for you!
Remember, You are not defined by your diagnosis. So don’t be unhappy with yourself. You are perfect in your own way, love your quirks, your personality, your face and body and learn to embrace your diagnosis. Be confident with who you are. Smile, it will draw people in, do not make your happiness about how you THINK others perceive you anymore. I am happy because I love who I am and what I do. I love my flaws ( and I have them) I love my imperfections because they make me, me and “me” is filled with goodness, love, kindness and caring for many. This is why I am devoted to being an advocate, the voice of many.
Have a terrific day… Thank you all for hoping on board of this amazing journey! I promise it will be worth it..
Remember… Epilepsy, Let’s talk about it.
Thank you to my son, family, my boyfriend and very dear friends for your love and support without it I wouldn’t be able to help so many.