Guest Blog by Mary Lawrence
Mary Lawrence relates her own journey with Epilepsy and her will to the live her fullest no matter where the road takes her:
“During my childhood and throughout adulthood, I’ve had trouble with my parents, mentors, and acquaintances understanding my epilepsy. Some called my seizures fits/tantrums or even disrespect. This program (EFOF) has given clarity and realization of details on this issue. I first became involved with EFOF after it was recommended by associates, family, and medical professionals after having a stroke and brain surgery in 2007.
I attend the support group meetings regularly and attend as many of the extra events that are hosted and sponsored by EFOF as possible. The support groups have made a difference in my life because I now have a place to go to learn more about my seizures, a place where I can learn more every month about epilepsy, speak to others who have been through what I’ve been through, and support others, as well. EFOF has provided resources in the area available to me, and it’s also helped me learn how to talk to others about epilepsy. The support group has especially been a great tool and resource for me and others.
These programs have changed my life by helping create new relationships and understanding while on my epilepsy journey.
In 2017, it will be the 10-year anniversary of my brain issues. In 1973, at three-years-old and after an intense seizure experience, it was discovered that I have a birth defect: a gap in my skull, indicating the bone tissue did not develop properly. At seven years of age, surgery was performed attempting to repair it. Every 10 years since then, I’ve had a problem from the surgery: at seven-years-old, uncontrollable temperatures; at 17, a seizure; at 27, a stroke; and at 37, a discovery of bleeding on the brain.
I will be 47-years-old this year. Who knows what will come next in my epilepsy journey – a mystery solved, hopefully. Although the year is still young, I may have discovered where the next chapter to this story will lead me. On March 4, I woke up with what felt like a sinus headache. By the following day I began having issues with double vision, but not the kind that can be treated with glasses. It is where I see things one on top of the other. I went to the ER at the insistence of my family and was admitted overnight for a CAT scan and MRI. No evidence of a stroke was found. Eye exams show that I have a clear vision in each eye, they just aren’t working together. But this will not stop me from living my life to the fullest and participating in as many EFOF events as I can.” — From the EFOF July Newsletter.
You can help ensure a better world for people living with epilepsy by including a charitable bequest to the Epilepsy Foundation of Florida in your will. A bequest is a simple way to help protect the future of our Foundation, and can be any dollar amount, a specific asset, or a percentage of your estate. For more information, please contact:
Vice President of Business Services
(954) 779-1509 | firstname.lastname@example.org