Why this Healthcare Fight is Important to Me

Why does it have to be a matter of either/or? You can either pay outrageous premiums, get a doctor who may not understand your condition, or go uninsured all together? Something has got to give in this broken system.

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7 Questions to Ask Your Doctor When Diagnosed with Epilepsy

I encourage you to be your own best advocate. Don’t be afraid to ask questions. Don’t wait until the appointment is over and wish you would have said something or got that burning question in.

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How Television Portrays Epilepsy

This post is part of the Epilepsy Blog Relay™ which will run from June 1 through June 30. Follow along and add comments to posts that inspire you! Every time I hear the word “seizure” during a television show I automatically start to cringe. How will it be displayed this time? Will it be a Read More

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Improve Your Life with Epilepsy by Practicing Self-Care

This blog post is part of the Self-Care Movement hosted by Self Care Catalysts. Learn more at www.selfcaremvmt.com. Use hashtag #selfcaremvmt on all social media outlets. What if I told you that you can change your life with Epilepsy by simply putting yourself first? If I also told you that practicing Self-Care would be the key Read More

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How My Fitness Wearable Helped Me Take Control of Nocturnal Seizures

This post is part of the Epilepsy Blog Relay™ which will run from March 1 through March 31. Follow along and add comments to posts that inspire you! Yes, my lovies I am back gracing the net again. If this is your first trip to my little corner then welcome. I’ve been away for a Read More

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Women, Hormones..Seizures?!

Cramps, seizures, fatigue, cravings for Twix, a root beer (ok maybe that’s just me) and pimples are sure signs my not so friendly friend is coming. Yes, I said seizures! If you didn’t know, a change in your hormones can definitely be a major trigger for seizures in women. These types of seizures are known Read More

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Technology for the Epilepsy World

This post is part of the Epilepsy Blog Relay™ which will run from November 1 through November 30. Follow along and add comments to posts that inspire you! We have reached the half way mark of Epilepsy Awareness Month 2015! Crazy how fast time flies! Let me start off by stating, this post is no Read More

The Journey Continues…

I can quote Forrest Gump all day long and that statement explains the last few months of my life perfectly. It has been filled with so many twist and turns. Some unimaginable events, some things I tried to prepare myself for but still was not ready for. Life has just been crazy. In the midst Read More

Beyond the Epilepsy Stigmas

This post is part of the Epilepsy Stigma Blog Relay which will run from June 1 through June 30. Follow along and add comments to posts that inspire you! Since seizures had a name and epilepsy was a known diagnosis, stigmas were attached. Epilepsy Stigmas are one of the toughest barriers to breakthrough. Society often Read More

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Do They Really Understand My Epilepsy?

  In life, we often go through things and look to others that shared similar situations, for support. We want someone who can say “hey, that happened to me too, or I understand because I’ve been there” and really mean it. We look for empathy not just sympathy in a sense. When it comes to seeing Read More