Friday, December 19, 2014

The Chelesa Foundation for Epilepsy in Winchester, Virginia



THE VILLAGE AND THE EPILEPSY LEADERS IN WINCHESTER

On Nov. 12, 2014 I was invited to come to the Chelsea Hutchinson Epilepsy Event to help raise epilepsy awareness. It was a very successful evening.




The event was coordinated by the leaders of the Chelsea Hutchinson Foundation for Epilepsy Awareness from Winchester, Va.  This couple is Steven and Carol Shafran who invited me to the event. I was selected to help MC the event and also share my book "The Village" and the power of the Village Concept to help educate society about epilepsy. The event was held at the George Washington Hotel in the area and the turnout was great! This included a Boy Scouts Group, individuals, and generations families which showed the support that was formed by the leaders. The information about epilepsy that was shared and how it inspired others attending to speak about epilepsy was incredible. My good friend and strong supporter, Art Yannucciello of Va. Beach attended and he was very impressed!

There was an official proclamation from the City of Winchester presented to the Shafrans proclaiming the month of November for Epilepsy Awareness. Also in the proclamation it recognized the outstanding work accomplished by the Winchester Friends of the Chelsa Hutchinson Foundation (Steven and Carol Shafran) for increasing epilepsy awareness and hosting various events including the annual walks held in Winchester. They received a standing ovation as this was presented to by the Mayor of Winchester.

I also shared with everyone my reason for writing my novel and the main character I had created to represent epilepsy, "Mr. Kevin Bolden." This all went over great as people were looking for individuals willing talk about epilepsy. Well they now have "Mr. Kevin Bolden." Our goal is to use my novel as an educational tool for society! I myself along with others want to see a movie done to help open the hearts and minds of people about epilepsy. I feel "It takes a village" of people to make a difference in the world of epilepsy and I feel I have found a village in Winchester, Va. I am "Thankful!"

Sincerely.
Lowell G. Evans
Author of: "The Village"- Representing society
Creator of: "Mr. Kevin Bolden"- Representing epilepsy
Email- thevillageiscoming@gmail.com

Thursday, December 18, 2014

The Mother and Son from Alabama Made My Day


Mollie Campbell <mc.molliecampbell@gmail.com>
12:49 AM (10 hours ago)
https://mail.google.com/mail/u/0/images/cleardot.gif
https://mail.google.com/mail/u/0/images/cleardot.gif
https://mail.google.com/mail/u/0/images/cleardot.gif

Why families need a "Village of Support" for Epilepsy
                                                                                                                                                                                                                                                                                                                       
                                                        

Mr. Evans,
My son picked up your book the other day and asked me to tell him what it was about. I had not had the chance to read it completely yet, but I spoke to you while purchasing the book at the expo in California. After telling him what I knew about the book he said, "oh mama, that's a book about me." My son is 8. His name is Keithan. He's had seizures since 1 1/2. He was finally diagnosed at age 4 after countless er drs, first responders, pediatricians, nurses etc had told me "he's fine. There's no need to call and ambulance or come to the er. He doesn't need to see a specialist." I was torn. For nearly 3 years, my mother's instinct told me one thing and the professionals told me something else. I was a young mother struggling to go to college and work as I could. You see, I couldn't afford daycare at the time and anyone in my family that was willing to keep him for little or no money was scared he'd have a seizure so they either found an excuse to keep from hurting my feelings or were just totally honest. It hurt but I did appreciate the fact that I had people that cared enough to not be over confident in their ability to care for him and just be honest with me. When he was finally sent to a neurologist, I just knew that I would get the answers I'd prayed for all that time. As I left the office, I looked back at his little self in my rearview and cried the whole 1 hour drive home. He asked me what was wrong and I couldn't say anything to him. I should have asked someone to go with me, but with what all the professionals had told me before, I guess a small part of me wanted to believe them. So, I took him by myself. When we got home, I went to my parents and told them the news. My 70yr old father broke down in tears apologizing. You see, my dad has epilepsy as well. He fought for our country and has faced many challenges that many men would crumble under...but knowing what his grandson was facing brought him to tears. My heart broke all over again. I did not blame my dad and it hurt me to know that he blamed himself. I told them how all the way home I wanted to stop at the hospital and pediatrician and beg them to tell me why they lied. Why didn't they tell the possibilities? Why did they give me false hope? These are people you should trust. I will never forget the paramedic that told me I didn't have to call them...I looked down at my child lying limp in my arms, not breathing normally. I kindly told him he could either drive my child to the er or get out of my way so I could. These are all flashbacks that went through my mind as the news sunk in years later. At that point I made up my mind that no person that came in contact with my child would not know about his condition. I also knew that the battle would be hard at times but regardless, I would promote awareness. I immediately began researching. True, I'd seen my dad have seizures for years. But it was different watching it take over my child's body. He started medication and the changes to our lives began. The preschool teacher would call, "do you care to come get Keithan? He's having a hard time staying awake." I'd get to the school and she'd be holding him like her own child. He had a seizure at a local splash pad..the lifeguard ran up to us and looked at him laying on the ground not moving.."he shouldn't have been horse playing!" His great grandmother not so kindly told the lifeguard what was happening and that he'd just stopped seizing. His entire attitude changed. My baby was less than a foot from a drain that was full of standing water. It's only by God's grace that he didn't land in the puddle. It could've been much worse. We went through a few hospitalizations, medicine changes, tests, bloodwork...everything eventually leveled out and the seizures didn't come as frequently. He started "big school" and that was a different struggle. Some of the higher ups didn't want to give him the plans he needed to succeed but I fought. Everything leveled out again.. I was just learning the roller coaster of epilepsy. I found out I was pregnant soon after my son was diagnosed. The first thing I asked the dr was about the chances of this baby having epilepsy...that's another thing I've leaned about epilepsy. There a very few "solid" answers. And as a mother, that's the one thing I wanted most other than to take the battle from my child and fight it myself. My youngest son, Carlin, was born in November. Everyday I prayed. Age 1 1/2 rolled around and Keithan and I were laying in the bed with him. Suddenly I felt the bed moving. I jumped up knowing what was happening..Keithan was having a seizure..only as I jumped up, Keithan jumped up as well. He was nearly 5, but he was smart. "Mama, bubba is having a seizure!!" He went crazy. Crying and screaming that I not let his brother die. Thankfully, Carlin has had normal tests results and hasn't had as much activity but I will always worry. I have been pretty much a single parent through all this. But I thank God for every struggle. While reading your book, I remember trying to work at a job making very low wages..and having to sign a form acknowledging that taking my kids to the er or dr would not be an excuses absence and would result in termination. I knew this would not be the job for me, but kept working until the time came that I had to take one of them to the dr. My only thought was, "how can they tell me that I will lose my job for taking care of mum kids?" But I was te one that signed the papers so I knew I couldn't argue. I just began to work as a substitute teacher and wash cars or mow lawns for money. My parents helped too. The more research I did, the more I came across terms like SUDEP. I then came in contact with the Emfit corporation. I could not afford one of their monitors, but the lady was nice enough to give me contact information for a group that may be able to help me. The Danny Did Foundation in Chicago. I left a message and made other plans. I called my local banker and explained lmy situation. We were to meet the next day. Thirty minutes before my scheduled meeting with the banker, Tom Stanton from DDF called my phone. They were going to pay the full cost for a monitor! God is good! I immediately asked what I could do in return. His only request was that I raise awareness for epilepsy. His 5yr old nephew died from SUDEP. I eventually did a bake sale raising $900 to go back to them. That would cover the cost of one monitor and half of another! So yes, you get what you give. Only they were gracious enough to give to me before I had the chance to return the favor. Seeing the support from my tiny town motivated me to organize the first ever epilepsy walk in our county. Somewhere around 50 people came. I think I cried the entire time. Especially when I introduced myself and honored the people with seizures/epilepsy. Three of which were my dad and two boys. My boys have faced more in their short lives than I have my entire 28 years. I gave birth to my heroes. They never stop. Even with all the issues that come with epilepsy besides the seizures. My oldest son has a best friend in school. He had leukemia. They stick to each other like glue and have since kindergarten. I did a little class for his classmates and explained about epilepsy. This was spurred on by the fact my child would come home from school crying because he'd felt funny during the day and was afraid to have a seizure in front of his friends. There have been times when I've talked to people about what my kids face and cry or have a lump in my throat. But when my sons best friend asks me to give him a "team keithan" purple epilepsy shirt...I know that we have a village too! This is the same friend that had leukemia. His name is Trevor and my son has a team Trevor leukemia shirt...the one thing I wish the world would understand is that epilepsy doesn't just affect you for the duration of your seizure. It doesn't affect only the person having the seizure. I have finally found a job that understands my children's illness and my need to be at their side anytime I'm needed. True, I don't make much money and we struggle, but I am working and my children are healthy. Many jobs won't keep you around if you have to miss work like I've had to do at times. I'm just thankful I found one that finally works with me. Not against me. I've had mothers or friends tell me they don't know how I do it. This always puzzles me. I want to ask them just what my other options are in their opinion , but I know that they only mean the best. I know I have rambled on, but I can relate to a lot of what your book is about. Epilepsy doesn't get the limelight it needs to get funding and research. The stigmas that go with epilepsy and the fear of the uneducated do so much harm. People in general don't even have the first idea as to what seizure first aid is. My children are my world. I know they're only loaned to me from The Lord. And I also thank him for givig them to me and trusting that I can take care of them even with this illness...at times I do feel overwhelmed but I look at them and see that they don't give up. So why can I be selfish and give up?! I can't. And I wont. From Stevenson, Alabama, you have a mother and two little boys who know what epilepsy can do to your world! Financially, emotionally, physically, and mentally. We are here, but please know we are now a part of your village. Please don't stop! If you ever come this way, please let me know. May God bless you. May He help us fight this and promote awareness until there is a cure! On the inside cover of the book we purchased, you wrote, "Keithan you are a winner! Remember you have epilepsy but epilepsy does not have you!" Yes! You're correct. And I plan to keep your book forever. I will give it to him when he is a little older and remind him of how far he's come.  Thanks to people like you, he will go far.
Sincerely,
Mollie Campbell

Sent from my iPhone

Thursday, December 11, 2014

The Letter About Epilepsy


LETTER TO ME AND MY CHURCH MEMBERS ABOUT "THE VILLAGE"

Lowell Evans:

I am taking this opportunity to bring awareness of how significant the impact of knowing you and your sharing of yourself has helped not only me, but my brother (Kirk Hawkins) as well.

It is indeed ironic that we have been neighbors for some time, yet never did our paths cross.  Rather, (as is always God’s way) at the right time, for the right reasons, (God’s time is a good time) we met and it has been an event (then and now) filled with ministering, testifying, and supporting one another. 

I thought attending and sharing in the joy of your book signing was a momentous occasions, and I could not have been prouder or happier for you.  Yet, the events that took place at my home on April 16th, solidified for me that which I had been telling you, “this book, your trials and tribulations, the lives you touch via your book” are a part of something greater to come. This book, your testimony and all that come with it, is your ministry.

As I shared with you, my brother (Kirk) is an epileptic. He had gran-mal seizures from early childhood until adulthood.  Eventually, (as an adult) he was told he was seizure free. Yet it was not the seizures that scarred him for life mentally and emotionally, it was reactions from our parents, (most especially my dad) extended family members, school administration staff, and friends that has forever (then and now) marked him. 

As a result of ignorance, my father (who was a man’s man and detested weakness in a male) screamed, beat, threatened, berated, belittled, anointed, laid hands on, and ridiculed my brother in an attempt to “exorcise the demons” that was bringing on the “fits”.  He (my father) was convinced there was nothing of a medical nature wrong with Kirk, but more of a “Spiritual” nature.  In Kentucky, the Bible was the key to all things known and unknown.  As such, if “laying on of hands” didn’t work in most instances, “laying on of the belt” (switches, drop cords, etc.) would. 

 

As word of Kirk’s abnormality spread through our small community, so did the whispers, giggles, exclusion from play with his peers (in case it was contagious), rumors spread labeling him as “retarded”, and viciousness from children and adults ran rampant.

Eventually, Kirk was taken to the doctors and massive amounts of Phenobarbital and Dilantin was prescribed.  Yet the damage was done. Nothing could be done (diagnosis or no) to sway people from their Bible thumping, demonic spirits, beliefs. The effects of the drug treatment plan in fact exacerbated their beliefs as he exhibited signs of drowsiness, being extremely lethargic, sometimes confused, and at times, drooling.   

When my brother graduated, he entered the United States Army. Shortly after joining, he had another seizure. For the first time he was given an effective treatment plan and reassurance that he was not a “retard”.

For the next 15-20 years (from about 1977-1999), our family never saw Kirk, and rarely did we hear from him.  In 2003, Kirk reappeared.  However, he revealed (to me alone) that he was not well.  Additionally, with much bitterness, he shared with me how his previous years of treatment with respect to epilepsy had destroyed his faith in people, almost caused him to kill himself, had led him to drinking to forget and caused him to separate himself from “family”.

When I met you (Lowell) and you shared your book and your life as an epileptic with me, I was impacted in ways you could ever know the full scope of.  The memories of Kirk being beaten were so very overwhelming.  I think for the first time in my life I understood just what he had gone through and I began to thank God for sustaining him in spite of it all. Sadly, my father (deceased since 2004) although enlightened about epilepsy, never truly accepted my brother had a true medical disorder.  As such their relationship (dad and Kirk) remained strained until his passing. 

On April 16th, I shared with you that I had not heard from Kirk in 2 years.  I knew of your desire to minister to him that “he had epilepsy, but epilepsy did not have to have him”.  Lowell, when my home phone rang and I saw Cell phone, Ind. on the caller I.D., I knew God had heard our pleas. What would be the odds of Kirk calling me on that day at that time after a 2 year silence?  Before I answered that phone, I knew it was my brother.

As you know, he shared with me he was calling to let me know the nature of his illness had prompted his doctors to inform him of a need to finally share and invite a relative into his affairs. Before I could wrap my thoughts around that however, his next words stopped me cold.  He said, “Sis, I can take anything except the possibility of those seizures reoccurring. I would rather die than have another seizure. But the Holy Spirit told me to call you because you have something or someone for my seizures”.  Lowell, I could do nothing except hand you the phone.  I could give no introduction, I could say nothing. But I knew in my spirit without a doubt you were meant to be in my home at that time on that day for my brother.  I handed you the phone that day knowing something bigger than epilepsy was going to take place.

Lowell, on that day, the over whelming presence of the Holy Spirit was in this house. Thank you for that day and the days that have followed since then. Thank you for being obedient to the will of God in your life.  Thank you for taking the time to speak with my brother on not only that day, but other days.  Thanks for your words of encouragement to him.

Finally, thank you and your church congregation for the last act of kindness you have shown my brother.  You took my brother’s name and depth of despair before the body of your church. Many, many members signed your book with in depth words of encouragement and promise to continue to Pray for him. I did not know of this act of kindness. Truly I did not know that you and my brother’s relationship had evolved to the point of you knowing his address.  My brother is a very private, reclusive type person.  Lowell, I don’t have his address then or now.

My brother called me to report he had received the book from you.  Lowell, I was in awe of my brother’s awe in knowing someone cared enough to send the book, that people took the time to write to him personally in the book, that an African American man (you) would reveal to the world he has epilepsy.  I listened as my brother quoted scriptures, praised God, and talked about his past and his anger at having epilepsy.  Most of all, I listened as my brother began to heal a little.

Lowell, my brother asked me to  tell you on that day that if you did not hear from him in awhile, not to worry, but the overwhelming feelings that book and the words of encouragement from the congregation was new and a little too much for him.  Yet, he shocked me by saying “sis, tells my story to Lowell or anyone. But make sure you tell it all”.

Lowell, Kirk Hawkins had epileptic seizures. But he finished school, mastered a trade (as taught to him by our father) as an electrician, served our country honorably in the United States Army for many years, became a husband, father and now a grandfather. He (like you) is the face of epilepsy.

My brother said he Prays no one ever has to have seizures, yet he thank God for avenues of education such as your book to put not just a medical term to the illness, but an instrument such as yours that will actually give a face to the illness.

 

Thanks again!

We (Kirk and I) wish you the very best in your endeavors now and in the future.    

6/15/11

Tuesday, October 21, 2014

Ms Deborah Parker Smith

A Lady from Alabama is Delighted in Reading "The Village"

Ms Deborah Parker Smith is a lady I met on the Internet and I share with her my desire to increase epilepsy awareness around the country. I also informed her of my novel, "The Village."

After reading my novel, Ms Deborah posted a picture of herself reading the book for me to see. The statement made by this reader and her picture posted 25x within a few hours and I was contacted by Ms Susan Noble of Epilepsy Warriors Foundation! She was so excited and share the news with me.

Truly, all that needs to happen is for us to "Speak Up" about epilepsy for the safety of everyone that is involved. Ms Deborah is just one of the many people I have reached with my novel, "The Village!'

Sincerely,
Lowell G. Evans
Author of: "The Village"
Creator of: "Mr. Kevin Bolden"
Email- thevillageiscoming@gmail.com

Wednesday, September 10, 2014

The Village Support Group

           PEOPLE WORKING TO MAKE A DIFFERENCE
 
 
Here are a few of the people who are working hard to help increase "Epilepsy Awareness" in the community. These individuals are making a difference in the world of "Epilepsy!"
 
We are asking for your support to help us reach the churches, schools, businesses, etc to help eliminate epilepsy discrimination and especially the bullying by sharing our stories with others!
 
 
 

Sunday, August 24, 2014

The Middlesex Epilepsy Seminar


I have been fortunate to have this family attend the "Middlesex Epilepsy Seminar" we had on Saturday, Aug. 23, 2014 in Saluda, VA. We all had a "Great Time" and a few surprise guests showed up as well.

The event gave everyone a chance to speak about epilepsy and how the condition is not always the biggest challenge but "society" also plays a huge part in this.

We will continue to press on to having a movie made to help educate everyone on this condition and to help eliminate the discrimination and bullying that we have heard others have faced!

Thank you!
The Village for Epilepsy Awareness

A New Reader!

This Lady has received the a copy of "The Village" and is sharing it with you! I am pushing for a "movie" to be made so that society can be educated about this condition known as Epilepsy!

I am "Thankful" for everyone who believes in The Village!

Thank you.
Lowell G.Evans
Author of: "The Village"
Creator of: "Mr. Kevin Bolden"
email: thevillageiscoming@coming@gmail.com

Monday, August 11, 2014

The Village

 
This is a book that will help "Bring Back" what we have been missing!
 
One Another!
The Village by: Lowell G. Evans

Tuesday, July 1, 2014

Massachuetts Recognizes, "The Village" by Lowell G.Evans

                                           Mr. Poncho Thompson of Massachusetts Says:

 
My classmate, my teammate, my friend, thank you Lowell G Evans for opening my eyes and the eyes of many, God Bless you my brother. I would like to challenge my friends and family, especially Gloucester High School Alums to match or better my purchase of $20 for The Village, show your support by contacting Lowell and order your copy, thank you.

       Thanks Poncho! My email is - thevillageiscoming@gmail.com

Tuesday, June 24, 2014

The Epilepsy Ten Network

                                        Tiffany Kairos of the Epilepsy Ten Network
                                                        Supports "The Village"

Tiffany is determined to help make the lives of individuals who have epilepsy much easier. She is has received a copy of "The Village" written by Lowell G. Evans and is helping to promote the novel to increase epilepsy awareness.

Lowell, the author and Tiffany met online sometime ago and they both realized they had the same desire to help others with epilepsy overcome the challenges in life. They both attended the National Epilepsy Walk this year in DC and have stayed in touch since.



Friday, May 23, 2014

I AM HAMPTON ROADS


"THE VILLAGE IS COMING"
 
 

Please see the link below for the show "I AM HAMPTON ROADS"

My novel "The Village" and the character I created, "Mr. Kevin Bolden" is changing lives all across the country.

My goal is to "Increase Epilepsy Awareness and Eliminate Epilepsy Discrimination."

Thank you for your support!

May God Bless,
Lowell G.Evans
Author of: "The Village"- Representing Society
Creator of: "Mr. Kevin Bolden"- Representing Epilepsy
Email- thevillageiscoming@gmail.com

Available online at:
www.barnesandnoble.com
www.amazon.com
www.lyrical4cast.com


http://wavy.com/2014/05/15/i-am-hampton-roads-lowell-evans/ I am Hampton Roads: Lowell Evans wavy.com

Wednesday, May 7, 2014

The Book Signing At MacArthur Mall




ONE OF THE BOOK SIGNINGS FOR
 
 "THE VILLAGE"

 
 
 
 
Just A Few
 
A Thank You from the "Kevin Boldens in Society"
 
 
Here is a picture of "Just A Few"
A number of people who support "My Call"
This photograph was taken at my "book-signing"
This was done in Norfolk, VA at the Macarthur Mall
 
These are just a few people who has seen God's Work
I am referring to the "Miracles" God has performed for me
But truly "None" of these Miracles came too easy
Why? I had not put my full "Faith and Trust" in thee!
 
It was brought to my attention after I had written my book
A novel based on "Epilepsy Education", which is a sleeper
A Man read my work and agreed the knowledge needed for epilepsy
He then said, "This is also focused on being, Our Brother's Keeper"
 
I thought for a second or two because of what he said
It written in a way so that anyone could enjoy the story
Yes, "Mr. Kevin Bolden" and many others have epilepsy
But because of "Just A Few" like you, they do not have to worry.
 
"Words from the Heart"
 
Lowell G. Evans
May 7, 2014
 
 
 
 

Sunday, March 23, 2014

"MY EPILEPSY MAY BE PRESENT, BUT I AM STILL A GIFT FROM GOD!"


HOW CAN YOU BE A DONOR? YOU HAVE EPILEPSY!

On Oct.23, 2013, Lowell G. Evans did a "Bone Marrow Transplant" for his sister, Rosalee Irvin (Ms Rose) who had "Leukemia." Many people questioned the idea of Lowell even being "tested" to be a candidate all because of his epilepsy. The fact is that the ones questioning this ''testing" knew nothing about epilepsy. There is a "Lack of Knowledge" of epilepsy in society and these individuals proved it.

 After the testing of all of the siblings in the family and Ms Rose's son, Lowell, the youngest child in the family was selected to be the donor. Lowell G. Evans, author of “The Village.” This again surprised many people as they wondered how that could be. The fact of the matter is that there is no way that "Epilepsy" can be transferred to the other person.

 The entire operation was a “success” and this was due to the "Excellent Health Condition" Ms Rose had always kept herself in. In 2010 she successfully completed the 3 Day Walk for Breast Cancer.  She always took pride in taking care of herself. She had no idea that she was going to be diagnosed with "Leukemia." Her "Positive Attitude" also made a huge difference in her recovery at Johns Hopkins Hospital in the state of Maryland.

 After eight (8) weeks of aftercare following the Bone Marrow Transplant, on Dec. 20, 2013 Ms Rose called her brother the, "Author with Epilepsy" to inform him that she was now Cancer-Free!

 Ms Rose and her brother Lowell with the help of God showed everyone “The Love that they have for one another.” Lowell then shared with society his new slogan, “My Epilepsy may be Present, but I am still a Gift from God!"

Look at what God has done!

Sunday, March 16, 2014

IMMANUEL BAPTIST CHURCH INVITES AUTHOR TO SPEAK


Article on March 6, 2014 from South Sentinel Newspaper, Urbanna,Va.

 




Lowell G. Evans

 

Author to Present Program on

Epilepsy Sunday at Immanuel

 

Lowell G. Evans will present a program on his new book, "The Village," and his experiences with epilepsy on Sunday, March 9, at 11 a.m. at Immanuel Baptist Church in Saluda. The public is invited to attend.
"I have written this novel and created a character named 'Mr. Kevin Bolden' to represent epilepsy," said Evans. "This idea has been very successful as I have been asked to speak at schools, churches, and organizations all around the area. I was also a guest on the Trinity Broadcasting Network (TBN) show ‘Joy In Our Town.’ This was a 30-minute talk show in which I was asked questions about my book and the epilepsy.
"Bolden was a man sure of many things but when his corporate job found out that he was diagnosed with epilepsy, the fate of his career and family became questionable," continued Evans. "Once 'The Village,' Kevin’s neighborhood, got a whiff of the inequality and unsatisfactory response of his job, it felt an obligation to rally together in efforts to help save his lifestyle and others that could be affected by the unfairness. For him, dealing with epilepsy was one thing, but getting people to understand the effects that it has on the person and their environment was a battle in itself. It would take 'a village' to win his life back.
"Kevin Bolden has epilepsy, but epilepsy does not have him; especially with the help of The Village!" he said.
He was born and raised in Gloucester. He is a member of the Middle Peninsula Epilepsy Support Group that meets once a month in Gloucester.
Evans has a passion for poetry as he refers to his works as “words from the heart” because God places the words on his heart, making it easy for him to put them on paper. He always believed in the old African American proverb, “It takes a village to raise a child.” With that in mind he was fortunate to have been raised in society where others believed the same.
After developing epilepsy during his college years at Virginia Wesleyan College in Norfolk from a fall while playing basketball, Evans was faced with some very “negative” thoughts about his future by his classmates and others who learned about his epilepsy. He was questioned about how he was going to complete school, how he was going to continue to play basketball, and how he was going to work and go to school at the same time.
Evans said what bothered him the most was "the fact that all of the questions and statements that were being made were made by people who had no knowledge of epilepsy.”
After years of dealing with the “lack of knowledge” of epilepsy, Evans decided he "would make a difference in the lives of others." His goal, starting with this novel, is to educate on an international level about epilepsy and to make life better for not only those with the condition but those who may one day come in contact with someone who is experiencing it.
With “The Village,” Evans plans to start a scholarship for high school seniors, using the theme of the book to help raise epilepsy awareness. “For decades, society has made life challenging for individuals who have epilepsy. Now it is time for an individual with epilepsy to take on that challenge for the lives of others!” he said.
"The Village" is available online at www.barnesandnoble.com and www.lyrical4cast.com. The book was published by Lyrical4cast Publishing of Newport News.
 

Saturday, March 1, 2014

Lowell G.Evans Author of The Village and Creator of Mr. Kevin Bolden

Author: Lowell G. Evans
 
 
 
 
The author of the novel, "The Village" and creator of character, "Mr. Kevin Bolden" Mr. Lowell G. Evans of Virginia Beach, Va, has been invited to speak at Immanuel Baptist Church on March 9, 2014 at the 11:00am service.
 
Lowell is a person who developed the neurological condition known as "epilepsy" from a fall he had in 1980 while playing basketball in college. After developing the condition he noticed the "lack of knowledge of epilepsy" in society. Lowell was advised to stopped playing basketball, reduce his semester hours, and consider twice before working a second job while in college. All of this came about because of the fact that he was now diagnosed with "epilepsy."
 
Again with the "lack of knowledge" of the condition he found there to be in society, he actually did just the opposite of what people thought he should not do. All of this was to prove that individuals with "Epilepsy" can still live a normal and successful life.
 
Year later Lowell, who is known for his poetry, decided to write a book to help "eradicate epilepsy ignorance" in society. This was done also because of the fact that he noticed that "people were not willing to admit to having the condition."
 
After joining Epilepsy Support Groups, meeting people on the Internet, researching epilepsy, the idea of creating an individual to represent epilepsy was decided. This is when Lowell created "Mr. Kevin Bolden." This character is a very successful, educated, corporate family men who happened to have "epilepsy." Mr. Bolden moves his family into a neighborhood called, "The Village." The youth in The Village come to know Mr. Bolden through his children but the adults of The Village never really take the time to meet their "new neighbor."
 
When Mr. Bolden has a seizure one day in the backyard while playing with the youth, they become scared! It is at this time when Mr. Bolden and his children "educate" the youth about epilepsy. Education is the "key" to understanding epilepsy as many people have been discriminated against because of the "lack of knowledge" of this neurological condition. Lowell's goal is to "eradicate epilepsy ignorance in society."  
 
Please come out to hear him speak at 11:00am March 9, 2014.The address of the church is:
 
Immanuel Baptist Church
PO Box 1139
317 Townbridge Road
Saluda, VA 23149

Thursday, January 30, 2014

THE EXAMPLE OF ONE "MR.KEVIN BOLDEN"

        Arkansas Man States: "Finally Someone Puts Epilepsy Into a Story!" ...

             Mr. Tim Parsons Sr. shares what "The Village and Kevin Bolden" has done for  him."

Hello,

My name is Tim. I recently came across Lowell Evans book, "The Village". I sent Mr. Evans the following message located at the bottom of this message...

I was amazed that someone had finally put in a story some of what I had experienced as a person with epilepsy myself. Although I have not read the book, I knew when I read about what the plot was what the book was about. This happens all too often in society today. It happened to me. I worked for the USPS from 1984 until late 1992 or early 1993, it was just before the Family Medical Leave Act was signed into law. I had begged my place of employment to let me do exactly what the FMLA gave workers the right to finally do. My meds needed adjustment after approximately 9 years of working, but my supervisors didn't like me missing work, even though I brought them explanations from my doctors about why I was having to miss work. Eventually, due to the stress and being made fun of by co workers, and with no help from EEOC I had a nervous breakdown because I could not get out of the hostile environment which was only making my situation worse.

I am sure myself nor "Kevin Bolden" are the only ones that epilepsy affects in this way, and the stigma that is attached to it by society is morally reprehensible. No one there saw anything wrong with what was going on.... I could not get any help from anyone, believe me, I tried. I was in the fight of my life, I had a family to feed and care for. If I failed in doing that, what kind of a man was I???

The reason I am telling you this, is that the story of Kevin Bolden, needs to be told, and told loudly. I have spoken with Mr. Evans, and it is like we have lived the same life, only a thousand miles apart. And I feel that there are a million other "Kevin Boldens" out there, who struggle everyday just to get up and go to work, knowing they too will have to face the harassment, and humiliation of being mocked, talked about behind their back and ridiculed afterward, all because they have, shhh, "epilepsy".
I was living the American Dream, and it turned into a nightmare for my family and myself...

Please help spread the word, and educate an ignorant population about epilepsy, and rid our society of the stigma associated with it.

Thank you for helping Mr. Evans, and thank you for allowing a small light to shine and reach me in what seems like a very dark and cruel world.

Sincerely,

Tim Parsons, Sr.
        

Saturday, January 18, 2014

THE VILLAGE TO THE RESCUE!


It was said, meet Lowell. He says,"I have epilepsy, but epilepsy does not have me!"

 A FAMILY IN NEED!
 
(THE VILLAGE IS THE ANSWER)

This letter is from a Parent that I was introduced to! Please read and understand why it was written!

Thank you,
Lowell G. Evans
Author of: "The Village"
Creator off: Mr. Kevin Bolden"


TO: Theresa Bowick, Conkey Cruisers


FROM: Tonya McKinney

DATE: December 17, 2013

RE: Lowell Evans and Epilepsy

Not sure where to begin except to say that our lives changed in 2010 when epilepsy entered our world. At the time, our 13 year old daughter had her second grand mal seizure within an 8 month period. After five days and many tests from her wonderful new doctor and neurologist (Dr. Toor) from the Children’s Hospital of the King’s Daughter in Norfolk, VA the diagnosis was given and a prescription shared. That was the easy part.

The difficulty began with Lauren being withdrawn. Because the seizure happened at a church lock-in, many teens witnessed the episode and were frightened. Many didn’t understand and became distancing themselves. Lauren had no recollection of the event and decided to retreat to the safe harbor of home. All extra activities and interests outside the home disappeared, as did most of the friends to come swim in the pool, hang out and ride bikes. Life as a "normal" teenager didn’t seem anything close to "normal" anymore.

Lauren began online friendships and felt safe there. She didn’t have to tell anyone about epilepsy, they didn’t know her and weren’t there that day. We also moved into a new house and new school, hoping that would help. Unfortunately only the location changed…epilepsy was still there at 8pm when we would take the daily dose of medicines to keep the seizures from returning.

One day at a community luncheon prior to a doctor’s visit to celebrate 2 years seizure free, we were told of Mr. Lowell Evans. A few days later Mr. Evans came to our home to share his story. This was the first time Lauren opened up to talk to someone about epilepsy, her lack of motivation in school or desire to leave her safe harbor of home. He gave her a copy of his book but more importantly shared with her that he has epilepsy, but it doesn’t have him. She smiled and opened up a bit. They became friends and he a source of support for her.

Mr. Evans has called many times on Lauren to encourage her to share her story, which ultimately is a story of God’s love and compassion through all. We like to say we are a work in progress kind of like a caterpillar morphing into a butterfly. As a faithful family, this strength is supported daily and encouraged to be what God desires, despite an epilepsy diagnosis and what others may think. We now look at epilepsy as an opportunity for perhaps a totally different plan in helping educate others in the future…coincidentally the very same idea Mr. Evans has! (At our house we don’t believe in coincidences, but rather the hand of God.)

I could go on and on about our gratitude for Mr. Evans. For the first time I see Lauren opening up, reading on epilepsy and actually talking about what has changed our lives. We try not to look at the negatives or fear the unknown, but rather try to bring good from this diagnosis. I hope you will find this helpful. We feel very blessed to have met Mr. Evans and look forward to spreading the word of epilepsy.

Thursday, January 16, 2014

"The Creation of Mr. Kevin Bolden"







The Creation of Mr. Kevin Bolden

A name and a face was needed for “Epilepsy”
              A health condition people are not always willing to discuss
          Still I felt that this was something people needed to understand
       So the creation of “The Village and Mr. Kevin Bolden” was a must!
 
Kevin Bolden was a hard-working, corporate, family man
Here was a happy husband and a loving father of two
All he wanted to do in life was to be very successful
So whatever price he had to pay, he was willing to do!
 
The people in his neighborhood, “The Village”
Truly admired him for the life he was trying to live
Unfortunately his Employer would not do the same
They saw his condition and put “Epilepsy” before his name!
 
Because of a “seizure” his Employer now saw him as a Liability
Instead of the “True Asset” he had proven himself to be
Mr. Bolden realized why they began to think like this
It was the “Epilepsy Education” that they seemed to have missed!
 
So he said, “Father forgive them, for they know not what they do”
But how could Kevin Bolden be the “Man” that God made him to be?
It was all because of the people in “The Village”
They saw a successful, educated man who just happened to have Epilepsy!
 
 The Village supported him during his trials and tribulations
For a “Good Husband, Father, and Friend was all they were able to see
Now Kevin Bolden is able to say to anyone, “Yes, I have Epilepsy”
But because of “The Village”, Epilepsy does not have me!”
 
“Words from the Heart”
Lowell G. Evans
Author of: “The Village”