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All Donations and Funds Raised will go towards Research for Epilepsy, Pharmaceutical Seizure Medications, Technology Devices for Seizure Management and Educational materials and the building of an Epilepsy Monitoring Unit and Resource Center in our local Childrens Hospital.
Mission Statement
To Empower, To Thrive, To Prevent, Control and Cure!
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41 Responses
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.
Thanks Erica I think you found the old page here is a link to the new one I am trying to get that fixed on the website!
http://www.facebook.com/groups/epilepsywarriorsfoundation/?ref=ts
Fantastic site keep up the good work, is it possible to place a link on my epilepsy site to yours?
Thank you Andy and yes by all means please do!!!!
Susan,
This is a wonderfful site and an amazing foundation!
Jen R.
Thank you so very much Jen I appreciate that!
fantastic site very inspirational lets just find a cure for dravet syndrome xx
Please contact us to see how we can help you with what you do.
(800) 556-0669
Thanks for inclusion and insight. 2 most important qualities of this site. Fills like family with a friendly atmosphere. Reassurance thru sharing ones concerns and tribulations. Very understanding and helpful encouraged by self participation without force or judgements. Going on 5 months. Time flys. Hopes for a cure.
Thank you for your formative information. It has answered a lot of questions. It has also raised a few questions that I now have for my neurologist.
Do you have a shortcut to your website page?
Thank you. Greg
Hi Gregory and thank you for the kind comment and visiting our website! I do not have a shortcut for the website I should look into that though! You can connect with us through our website to both facebook and pinterest!