Seizure Disorder: After the Diagnosis

Much of the time questions arise immediately after the diagnosis of seizure disorder.                                                                              doc_pat

Is there a cure?
What does this mean for my life/future?
Where do I go for support?
Will I be able to live a normal life?
Do I need surgery?
Will this impair my overall brain function?

…and the list goes on.

We at National Seizure Disorders Foundation understand the emotion and we understand the need for answers. We live with seizures and we care for others that live with seizures. We are connected with you on this level after the diagnosis. On an important level, you are no longer alone.
Answers to many of your questions will be specific to your diagnosis. NSDF steps in where many doctors fear to tread. We become involved on a personal level in your journey with seizure disorder, whether epileptic or non-epileptic. After your diagnosis, overcome the fear by connecting with us:


Beacon of Hope for seizure suvivors and caregiversNSDF Home Office: 615-326-0449 (in Tennessee)
Postal Mail:  NSDF 228 College Street Burns TN 37029

Why is it so important you contact us, or someone you trust, after your diagnosis?
The following fact is perhaps one of the most important reasons for gaining positive support, powerful resources, and knowing there is Hope for a higher quality of daily living:
The University of Maryland Medical Center enlightened readers of their website with this fact concerning the effects of Epilepsy and other seizure disorders on Adults:
*Psychological Health. People with epilepsy have a higher risk for suicide, particularly in the first 6 months following diagnosis. The risk for suicide is highest among people who have epilepsy and an accompanying psychiatric condition, such as depression, anxiety disorder, schizophrenia, or chronic alcohol use. All antiepileptic drugs can increase the risk of suicidal thoughts and behavior.
What can be done to  prevent this risk? Immediately after the diagnosis, seek help from positive and supportive seizures survivor groups, family and friends, and medical professionals including therapists. National Seizure Disorders Foundation, although we are not medical professionals, provide extensive online and offline support in order to help you understand your diagnosis, your treatment, your prognosis, the risks involved, and the possibility to improve your daily quality of life.
The staff of National Seizure Disorders Foundation  appreciates you stopping inTY today to take time to learn what you can do after the diagnosis of seizure disorder. Please take a moment to visit other areas of our website. With your help we are growing daily in order to become a quality clearinghouse of information, a beacon of Hope in turbulent sea of seizure disorder, and a reliable hub of resources and support bringing millions to discover positive seizure management.



*Source: Epilepsy | University of Maryland Medical Center

Author: Terrific Tonya Heathco

There's only one Terrific Tonya you are looking for when you are looking for empowerment over seizure disorders and stigma. I am the one to come to when you need help bridging the gap of fear and entering Peace in your seizure journey. I have the personal experience of 30 year(+) as seizure survivor, 27 years as caregiver, and experience as empowered advocate since 2008.