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All Donations, Funds raised will benefit not only our foundation but our warrior ambassador families. These families are chosen by us and will be supported over the course of a year to help alleviate some of the financial struggles they face in the daily living and management of epilepsy. The Epilepsy Warriors Foundation is a federally recognized 501c3 non-profit. All donations are 100% tax-deductible, and we thank you for supporting our children and families.
Wonderful Website! A million thank yous to you!
We are so PROUD of you! This is the best ever! YOU ROCK and we LOVE YOU SO MUCH! You have made a BIG Difference already!
Susan, this is a fantastic website. I love the layout and the information provided. You have done a fabulous job, keep up the great work in promoting Epilepsy awareness.
Susan, Keep up the amazing work! Thanks to people like you together we will find a cure! Lots of hugs for all the hard work you put into Epilepsy every day! Love, Gia and Wendy
Susan: What you have done here is nothing short of remarkable! Keep blazing that trail – you are a true inspiration!
What a great website and a FANTASTIC resource. Keep fighting the good fight; you are doing amazing work!!! Hugs to you and your team!
A great website Susan with a ton of information! Thank you for including my book in your library. We’re both working toward a similar goal of bringing more awareness to epilepsy so if I can be of any help, please don’t hesitate to ask. As I would say in my mantra “With a positive attitude anything is possible!!”
This is a beautiful site, very informative. I love this page so much
Thank God there are people like you Susan who take action where it is so greatly needed. God bless you as you move forward on this new journey!
Susan, I love the website. It is very informative and resourceful!! Thank you so much! The only way to find a cure for Epilepsy is through awareness and education and you are doing so much. Riley and Camryn’s epilepsy is so different and these resources have helped so much!!
Hey Susan,
Looks great! Thanks for all the work you do. This is what we need to bring attention to epilepsy to one day find a cure.
The website looks just incredible – I know it was quite a bit of work, but well worth it! It will be so helpful for so many.
Your Comments
This is a Fantastic Website. You are doing so much for our Children and everyone with this…You and your team are making doing Great things. …Thank you so much…..
Your Comments
The site is great. Such a great resource for families affected by epilepsy!
Congratulations! I really like the new design and layout of the website. You have done a great job and poured your heart and soul into the foundation Susan. I’m proud to call you my friend and fellow advocate, you are a wonderful person 🙂
What a fantastic site! It will be a great resource and blessing to many families to come! My best to you in this.
Glad you found your calling Susan! I’m sure many will benefit.
Thank you for sharing Gia’s story !
Keep up the great work!!!
Your making a big impact and difference for all our kids and family members with Epilepsy and I am so very proud of you. You never give up and you fight all the time for what’s right and to rid what is wrong. Your a great role model for my Kids and I love you…
Your AMAZING! I appreciate every thing you are doing to raise awareness about epilepsy! Truly amazing! Thank you so much, your website looks awesome. Your awesome Susan!
Wonderful website Susan. Thank you for doing so much to raise awareness of epilepsy and it’s affects on those who suffer from it.
Thanks for the insight, words, education. The site looks absolutely awe inspiring. Your reply and post to the view Celeb, was both thought provoking and synopsis of seizures. Even thou every American knows about it from Ceaser of Rome. I believe he suffered from fits, which was read about in a play …. the ides of march. I trust this will be a longtime reference that will not only be of help for my family members but others in our military. Nick Retired CWO3 USArmy 70-92.
I’m so proud of you Susan!!! It’s seems like just yesterday we were two facebook buddies who hated epilepsy and did everything we could to spread awareness & concern and now I’m with the EFGC and you have Epilepsy Warriors!!!! We are both in the right places! 🙂 The site is just great! You are truly making a HUGE difference in the world of epilepsy! xoxoxo!
Thank you so very much everyone for the kind words and comments. I am so truly blessed to be surrounded by such loving and supportive family and friends. We WILL WIN THIS FIGHT! 🙂
The website looks great Sue! I am honored and excited to work with The Epilepsy Warriors Foundation! We will plan a great launch party for this great cause!!
Thank you Candace, I am honored and excited to have you be a part of us and am so looking forward to your planning many great things for our Foundation.
This Website Is So Uplifting. I Enjoy Seeing the Updates and Reading Passages. Thanks For All You Do.
Erica, Thank you so much for those kind words. I would love and be honored to share your website link to mine, I just took a look its amazing and your Cousin Jazlyn is one beautiful and special little girl to have such a beautiful and loving Cousin. If your on Facebook would love to have you join our foundations facebook group page and feel free to request me as a friend!
Susan, thanks to you, my goal is somewhat easier to reach, getting people aware of this disease is what builds a foundation to a cure. I believe your website is definitely user-friendly and details the problem and shows a solution. As for my website, I appreciate your gratitude and comments as well to my effort, for my thanks, I will show more existance of your site onto mine, and I would love to join on Facebook! Thank you for the offers and thank you for helping to save a life.
Thanks so much Erica, we would love to Welcome you on our facebook group page so go directly to Facebook and look for our name and logo. Thank you again! Praying for your Cousin Jazlyn!
I Appreciate That So Much, You are a wonderful person, I hope you know that. You’ve Impacted so many lives. Again, Thank you. I Found your group. 🙂
Susan, thank you for having such a useful website and being a great resource for so many patients and families!
I have deeply enjoyed the ability to gain and hopefully to give encouragement to others who endure Epilepsy. I also have Spastic Cerebral Palsy which I don’t address very often.
I really enjoy being able to share the “Wallpaper” I share with the desire to be of some kind of visual encouragement or joy with others.
Thank you Susan and the others here for the encouragement which is shared.
Wonderful website for the research paper I’m doing! As an epileptic myself, this opened up many new doors of information! Thank you greatly!
This is awesome what you are doing. I am a help with Epilepsy Nebraska I am also a teen this is really cool to see what your doing. Hope all is going good in FL.
I have two sons with epilepsy. My oldest, 27, was diagnosed 10 years ago and my youngest, 21, was just diagnosed three weeks ago. I live on the central west coast of Florida. I’m having difficulty finding support for parents of adult children with epilepsy in the Tampa/St. Petersburg area. It’s a whole different game when your child with epilepsy becomes an adult with epilepsy. When they want to live on their own, issues with not being allowed to drive, getting their first job, social settings, dating, side effects of meds, etc…. The list goes on and on. While I feel I’m educated on some issues related to epilepsy, there’s so much more to learn and to share with other parents. Also, the public in general needs educated. I’ve been told so many times, ” So he has epilepsy. There’s medication for that. If he just takes the meds, then he’s ok, right?” Some even believe it’s a mental health issue or leads to mental illness. Is there any support in my area from the Epilepsy Warriors? If not, can we establish some?
Hi Lisa,
I don’t have a support group in your area but their is one for adults out of Tampa General they meet on a Wednesday evening once a month! Here is the information for you!
Epilepsy Support Group
This group provides a forum for people who have epilepsy and their families while also providing an opportunity to learn more about epilepsy, the challenges of living with epilepsy and available treatment options.
Dates: Meets the 3rd Wednesday of each month
Time: 6:00 p.m. – 7:30 p.m.
Location: For room location, please contact (813) 844-4675
Contact: Valerie Kelley, (813) 844-4675;
Hello i live in Alberta Canada . I live with epilepsy.. I don’t let it get me down ..
i hold a job that get’s me threw the year. i don’t have many friends, that is o.k
rock”en” roll live your life GOOD
Hello! Just saw your wonderful video and epilepsy month message. Congratulations on getting the word out!
Best…Ann Marie
This website is a wealth of information. I am a parent of a child just diagnosed in July
Hi Nicole, Connect with us on Facebook and let us know if we can help in anyway!
On May 30, 2015 I became the mother of an angel taken by SUDEP. I am looking for a place to turn my grief into something positive, and came across your website. I live in Southwest Florida, and am more than willing to help spread the word. I was not even aware of SUDEP until AFTER my son passed. A special thanks to all the warriors out there, and my heart goes out to all who are living with epilepsy.
My Warrior was taken home in July of 2014. He was my son, 25 years old and had Epilepsy for more than a decade due to head trauma in a car accident. I just wanted to thank you for the work that you are doing. I live in California and know that even in the most populated of cities there is not enough information, awareness and support for our Warriors. May Gods’ Grace be with you as you continue this very important work.