Epilepsy,  Personal

Don’t Feel Sorry For Me Because I Have Epilepsy

It’s never easy when someone that you know or someone that you love has just been diagnosed with a chronic illness. What can you say to show that you care about them and the challenges they must face? Oftentimes, it seems as though the only words to offer are, “I’m sorry.” As if the sun will no longer shine and tears of heartache will flow endlessly like a waterfall.

Yet I say to those who genuinely or without thought offer sympathy, don’t feel sorry for me because I have epilepsy.

Don’t feel sorry for me because:

  • I’m glad I was given a second chance in life.
  • I learned the true meaning of gratitude.
  • Fractured relationships with family have repaired themselves and grown so strong.
  • I’ve fallen in love with taking the truest care of my health.
  • The littlest of things capture my attention and heart.
  • It is apparent how fleeting time is so I do best to set fear and worry on the sidelines and live.
  • I make sure to try and never go a day without telling those that I love, “I love you.” Three words, three magnificant, meaningful words.
  • I’ve been given an opportunity to offer solace, hope and motivation to those who are on the same journey as I. Within this circumstance I feel honored and I smile.
  • Rather than hide behind my condition in shame, I stand on high, shouting and proclaim. Yes I have epilepsy. No it is not ideal, but I refuse to let it keep me down. This is my life and it doesn’t have me.
  • My relationship with my Lord and Savior has strengthened hard as rock. My rock in whom I take refuge in troublesome times.

Would you rather people not feel sorry for you because of your epilepsy? What reasons would you give? Share in the comment section!

I am a happily-ever-after wife, an Epilepsy Diagnosee, Advocate for Epilepsy Awareness (The Epilepsy Network), life lover & Christ inspired! Life is a journey and I'm loving every moment of it. Even the bumps in the road!

2 Comments

    • Christopher Rand

      I had epilepsy since I was born and at 3 months My parents were told I was not suspose to live beyond 3 months.

      I had taken so many anti seizure medicine and yet no help.

      Here are the medications I was on….

      Attivan
      Lamictal
      Tegertol
      Mogadon
      Depakane
      Depakote
      Dilantin

      I was in every Hospital you can think of and that is……

      Canada: London
      USA: ACH
      Akron General Hospital
      Cleveland Clinc
      Boston Children’s Hospital

      In 1998:

      I had testing done to see where my seizures were coming from and I had a 24 hour eeg around the clock.
      The doctors found out After I had 3 temproal
      Lobes in my right side of my brain.(
      That’s when I got a miracle from god in the neuro surgery in Cleveland clinc.

Leave a Reply

Your email address will not be published. Required fields are marked *

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

This site uses Akismet to reduce spam. Learn how your comment data is processed.