Sign our guestbook to show your support and interests for a cure for MS.  Thank you for your continued support!

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Ronnetta 'Roni' Waiters & Tammie Montgomery on August 19, 2010 at 11:24 AM said: hello cousin, well you asked me to stock by and check the website out so i have and im aware of how important it is for people to know. so my girlfriend and I are on aboard to support because we also we be starting a foundation for something. IN THE NEAR FURTURE I WOULD LIKE FOR US TO PLAN AN EVENT TOGETHER AS U SUGGESTED. LOVE YA

Lenny Harris on August 12, 2010 at 12:39 PM said: Ms Myers I want to thank you for your effort to get the word out on MS.

Kimberly Waiters-Williams on July 8, 2010 at 04:00 AM said: Hay Cousin, I am very proud of all your profound efforts to educate me and others who are unaware of the syptoms of MS. Now, that I have read up on the website, I am with you for the long hall of finding a cure and well as helping others. I love you and you can count me in for Stomping MS. Love you much, your cousin Kimberly. I will however, solicit some support here in Fayetteville, Lumberton, Rowland, Maxton, and Lauringburg, North Carolina.

Shamill Tucker on January 4, 2010 at 07:13 AM said: Happy New Year Cousin, I want you to know that I'm here for you and keep up the good work. I have a friend who would love to donate to the foundation so I will be giving them the link. Will talk to you soon... Love You!! Millie

Jayne Withers-Short on December 15, 2009 at 08:33 PM said: Hey Tamika, Wow, you are amazing, but I didn't expect anything less from one of the Myer girls. I'm very proud of you. Continue to fight the good fight. If there is anything I can do to support you in this effort, please let me know. Love, Aunt Jayne

The Maryland Pro Basketball Team Supports on December 13, 2009 at 03:37 PM said: Hello Ms. Mimi, As owner of the new Maryland Pro basketball team, The Maryland Marvels, I can't express enough thanks for performing and lending your talents at our next game. We are glad to support your cause. Take care, James Agbai

Tiffany on December 11, 2009 at 06:59 PM said: Love you Miko....Keep up the great everything!!!

Mr. Wylie J. Myers on September 22, 2009 at 06:45 PM said: Hi MECO! Keep on pushing because you know I am with you all the way. The few,proud and Amry Strong. I love you, DAD"

Ramona L Archie (Mona) on August 8, 2009 at 08:54 AM said: I think it is wonderful that you are fighting this. I help with children that have MS and I see some parents that won't do anything to help there children. They either think there is no use or just fully don't understand about MS. I will pass this site on to all of my friends and customers. I will also be praying that God will help get the word out and find a cure. I will make sure you are prayed for daily! Keep up the fight. Many Blessings, Mona

Corey Barnes on May 8, 2009 at 03:16 PM said: Tamika, The time has come to shine and hopefully on August 22, 2009 in Pageland, SC the torch will be ignited to bigger and better things concerning your foundation. I've watched you dedidicate yourself to this battle religiously and to be honest, I haven't been there fully as I should, but you know I've had my own set of circumstances. Now that my mothers situation seems to be headed in the right direction, why no change the face of the game. Obama's Presidency just reminded me that you can persevere any obstacle as long as you are focused. I know that I need my favorite cousin and my mother well, so this is my official dedication to helping out. Hope you accept my invitation to Stomp a cure into MS. Fortunately Lymphoma can be cured, but theres still ways to support those who battle it. Not all are placed in a position as my mother to have some of the worlds best doctors on her team, and we not even a famous family in the eyes of the public, but in Jesus's eyes all life is precious. All families are famous and we know that you and my mother both love God so that's why favor is granted. Enough said! Corey 1st Class Promotions

LAURIE HERBERT on April 18, 2009 at 10:32 AM said: IGIVE THANKS FOR YOU. YESTERDAY YOU PERFORMED AT THE MS LUNCHEON. IT S MY THEME SONG WHEN I START MY CAR - NO ONE IN MY HOUSE WANTS ME TO DRIVE! MY TYPING IS IMPERFECT BUT FOR IMPORTANT THINGS I DO TRY. AGAIN - THANK OU.

Raiya on February 8, 2009 at 01:46 PM said: Hi Auntie!! I am soooo proud of you. I would love it sooo much if you came to talk to my school about it. I know they probably don't know about it and i think they should. I know there are kids with parents who have it and i think you're the best for pushing forward and living life to the fullest! your foundation for ms is great and i think they should recgonize it as well just like they do for breast cancer and aids. ms is deathly as well. you probably didn't know but my mom's friend had it and she died. it was horrible, i think someone should stand up and say i will find a cure because this disease needs one. sooo thank you for standing up fist and god bless you!! love, rayray

Billie Brewer on January 14, 2009 at 12:30 PM said: I too was dignosed with ms on May 4, 2000. I too thought my life was over....my aunt passed away with ms. I later found out that it wasn't ms she died of....It was the medication side affects. Actually there was no treatment for ms when she was dignosed (in the 1950's). My symptoms were alot less exptreme than yours. I went blind in one eye....two weeks later I got my sight back. My twin also has ms. She was dignosed in 1994. Her sight was also effected. She now has to use glasses. The only thing wrong with me is my left leg....I have drop foot, a knee that buckles, and I can't lift my leg every high....I use a walker to get arround. I still can drive a car....thank God for automatic transmissions. I work fulltime and very active in my church. My attitude is: I have ms, ms doesn't have me!!! I know God has blessed my through my struggles.

Sharon Peeples on January 9, 2009 at 03:45 PM said: My daughter Tammy was diagnosed with MS in 2008 but from all of the things she has thus far undergone, we know she has had it for a long time. She has had 3 surgeries recently and has not had a chance to continue with the MS testing to see what ty0pe she has, but we believe she most probably has the relapsing/remitting type. I am so frightened for her and would really appreciate some one-on-one support from someone but don't know where to turn. Please pray....God is our only hope. ~Sharon~

Ebonie on January 9, 2009 at 11:59 AM said: I have a cousin who is experiencing MS right now. I do not understand what she is going through but I would like to help in some way. Like many, I only have a small understanding of what it is and how it affects the body. So,thank you so much for creating this site in order that people may become more aware of MS.

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