Susan Noble
Susan and her family reside in Fort Myers, Florida otherwise known as her little slice of paradise. She enjoys spending time with family, friends, and helping those in need. You can reach out to Susan for information about the Foundation or about Epilepsy at susan@epilepsywarriors.org. You can also visit the Foundations Fan Page on Facebook.
Susan Noble
Susan Noble

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Susan Noble

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Sudden Death Due To Epilepsy

Sudden Death Due To Epilepsy

November is Epilepsy Awareness Month. We will be hosting a month long campaign that will provide valuable information, facts, resources about Epilepsy, and what you can do to not only manage the day to day living with epilepsy but also become a voice to be heard. A crucial important fact regarding epilepsy that needs to…Continue Reading

Purple Day is a Day to Support Those Living with Epilepsy

Purple Day is a Day to Support Those Living with Epilepsy

Purple day is a day that is celebrated around the world to help focus and bring awareness for those who suffer from epilepsy and seizures. This day is celebrated every year on March 26th. It is an international grassroots effort dedicated to increasing awareness about epilepsy worldwide. We celebrate this day in the hopes that people…Continue Reading

How to Avoid Over Committing Yourself

How to Avoid Over Committing Yourself

One of the things I constantly seem to do is over commit and spread myself too thin. Why? Because I find it hard to say “ NO”. I want to do everything and be able to help everyone that asks, but in reality I cannot. I found that out during this last year so I…Continue Reading

Setting Goals For The New Year

Setting Goals For The New Year

2014 it is the start of a New Year, new opportunities, new blessings to look forward to. A clean slate or fresh start as some like to say. I am a very goal oriented person, very goal-oriented person, and very detail-oriented. I like lists and having things in order so when I set goals if…Continue Reading

Spreading Epilepsy Awareness

Spreading Epilepsy Awareness

Another year has just flown by and it’s that time again time to Rock the world Purple! Epilepsy is not just an American disease it’s a global disease. This is the time to spread awareness so that we can help our children / family members with epilepsy realize their hopes and dreams of living a…Continue Reading

Special Mom’s on Mother’s Day

Special Mom’s on Mother’s Day

They love unconditionally, they encourage, support and guide us through life and are always there to pick us up when we fall, or to wipe away tears when that boy or girl breaks our hearts for the first time.  Mothers of children with special needs and all moms are inspirational; they are fighters, they are…Continue Reading

Doctor Patient Relationships

Doctor Patient Relationships

Since becoming an advocate for Epilepsy another topic that seems to be continually brought up is that of Doctor Patient Relationships. It seems to be a topic that gets a lot of, well for lack of a better word, criticism. I hear things such as:  They never listen to me They think I am the…Continue Reading

Spread the Word to End the Word

Spread the Word to End the Word

Retard a word in the English language and one that this past week I have heard used not only by some children but by grown adults, our sports athletes, our celebrity’s and family members all in reference to other children some with special needs, to adults, to our President and other government officials. It is…Continue Reading