Welcome

Welcome to The Matt White CureALS Foundation website.  

 This website is designed to educate, entertain, and even inspire.  By sharing the events of my life and my daily struggle to live with ALS you will learn how I do it, see the fun and interesting things someone in a wheelchair and on life support can do, and maybe you’ll find a way to try or do something you’ve never thought possible. 

ALS is a horrible disease.  It robs its victims of all of their voluntary muscles including the diaphragm which causes those afflicted to suffocate and die.  I have lost the ability to use my arms or legs.  I can’t speak, or chew food or swallow.  I cannot breathe.  I get my food through a tube and my air from a machine.  I move around with a wheelchair and I communicate through a computer.  I also love every minute I’m alive! 

With the help of a loving wife and family and generous support from friends I’m able to do many of the things they can do.  I go to the beach, theatre, and restaurants.  I read and write and follow my favorite teams.  I entertain friends, and relax by the pool with the sun on my face.  I enjoy the smell of fresh oranges, the feel of the wind whipping across the water, and seeing the sky turn pink every night at sunset.  I laugh at good jokes, cry during sad movies, and wonder about whom our next president will be.  I spend more time fishing than I ever did golfing.  I constantly think of ways to do things and ways to do them better.  I’m one of the fortunate few who live with ALS, and I’ve chosen to make the most of it.

 Making the most of it includes raising money to find a cure or treatment for this insidious disease.  Since creating The Matt White CureALS Foundation dozens of fundraisers and generous donors have contributed hundreds of thousands of charity dollars to this cause.  I take the responsibility of distributing this money very seriously.  Only the most progressive, active, successful, and promising researchers get disbursements from The Foundation.  100% of the money donated to The Matt White CureALS Foundation goes to ALS research.  All administrative, fundraising, and operating costs are paid by The Foundations Board of Directors, so your tax deductible donation will be used for the purpose you intended.  There is little that I do that gives me greater satisfaction than raising money for The Foundation.  Feel free to use this website to make a tax deductible donation to finding a cure for ALS. Please enjoy the website, and thanks again for visiting.

Matt White

Chairman

Matt White CureALS Foundation

210 Capstan Drive

Cape Haze, FL 33946

IRS 501-c3

Tax ID 71-0941815

19 Responses to “Welcome”

  1. Marv Eastlund Says:

    Great website, Matt and Shartrina! I am really proud of you.
    Marv

  2. gary+max Says:

    we hope your efforts lead to a cure for als quick! we love your website. england isnt bad, but we cant wait till we visit florida again.

    your friends,
    gary+max

  3. Kevin Davis (Rick's bro) Says:

    Hello, Matt!! Great website…it is educational for sure. Keep up the extra effort. Hope to get down with Rick this spring to hang out and do a little (or alot) of fishing!! Thanks, for the 2007 Superbowl Pick ‘em. I was able to get some co-workers involved as well. Take care, Go COLTS!!!!!!!!!!!!!

  4. Meredith (former Q101 sales) Says:

    Matt-
    Just found your website. Oliver and I are thinking of you and feeling so inspired by your courageous story.
    Thanks for sharing your heart!

  5. CONNIE WILFONG Says:

    my brother 37 yrs old was just diagnosed with als. i just wondered if you tried any of the natural healing remedies, clay baths, detox, etc… if you did, did they help you any or is my brother throwing away money he doesnt have?

  6. Myles & DeAndre Says:

    Hey Matt! We’ll make sure Mom has lots of memories while she’s down here for the week so she can tell you about them. We’ll be coming down soon though! Can’t wait!

    Love you

  7. Pat Harrison Says:

    Matt, you are a true inspiration! I lossed a friend to the same thing you are suffering from years ago and I will never forget him. You give people hope and courage. God bless you! I admire you more than words can say.

    tight lines..

    Pat H.

  8. Billie Says:

    Hi there Matt.
    My Husband Bryan died of this terrible disease at the age of 44 in 2002. He too had chosen to live with the disease instead of die from it. And….he did live with it for 10 yrs, diagnosed when he was 34, he had a zest for life and a great love for his friends and family.

    I am happy that you are able to live comfortably with this Awful disease and am sure that your wife has to be an amazing person. I know you must think about others that have this disease and are not as financially secure as you are. These people that do not have a support system are those that sadly are not able to “live” with the disease, and are forced to die from it. Thank you for all that you are doing to help. May God bless you and yours and know that I will be praying for you .
    Billie

  9. Marsha Lucas Says:

    My father, Al, died from ALS almost 7 years ago. He was 79 years old. Since then I have been connected with the ALS Recovery Foundation in Miami, Florida. We have a Run/Walk every year during Mother’s Day weekend and raise a decent-sized amount of money to help end this disease. Hang in there and good luck. Life can be wonderful no matter what.

  10. Chuck Hummer Says:

    You guys have a powerful site here. I got here because of the excellent video for the head restraint. The question on appropriate head restraints is raised consistently on the Yahoo Living with ALS group, and the reference to your site and video is one of the most useful I have seen.
    I am also on the same journey and doing my little part to raise awareness and advocate for us PALS. Sites like yours do much to carry our message. Thanks.

  11. Gwen Brower Says:

    Matt& Shatrina,
    Your interview on WBCL was awesome! I’m sure that the message that went out over the radio waves will serve to be a huge blessing and encouragement to many, many people. Thank you for taking the time and making the effort to share your lives with all of the lives that you have touched and effected this day.
    Much love to both of you, Gwen

  12. Michael Says:

    Truly inspirational Matt! Kudos to the both of you. May you both win the greatest football pool of all time. Hail zookeeper!

  13. Andy and Brenda Says:

    We had a wonderful stay in FL this past week, and I can’t tell you enough how incredible it was to meet both you and Shartrina. Thank you for welcoming us into your home and allowing us to be there during your interview with WBCL. After the interview, you both just continued on about your day and Shartrina brought you outside in the sun. How remarkable it was to see love so clear. The strength and kindness of your family brought us overwhelming joy. More than ever did we see that each day is what we make of it.

  14. Rob Says:

    Matt,

    Your courage is an inspiration! I came to your web site via Steve Rickel. I am proud of him for his recent accomplishment of completeing the Philadelphia Marathon. I now know where much of his motivation and strength was derived. I hope your happiness continues for many years!

    Rob

  15. Ed Frierson Says:

    Hello Matt & Shartrina,
    My daughter, Julie Patterson, from WISH TV in Indianapolis hooked me up with this website. When she visits in the spring, we will have a “celebration of connectedness.”
    Ed

  16. sandra k morgan Says:

    great site! Bobby on plm directed me to here. thank you for all you do.

  17. Max Dziabis Says:

    Hey Matt and Shartrina! We’re moving to the States in April! Expect to hear from us soon. Anyway, I’m doing my medical project on ALS.
    Bye!
    PS: Shartrina, next time we come, I’m bringing Back to the Future! :-)

  18. Adrienne Apple Says:

    Hi, it’s Adrienne, Julie Dimond Apple’s daughter. I hope you’re doing well right now, and wish you the best of luck. Maybe the money you donate will help fund the cure’s breakthrough. =D

  19. Mitchell Brower Says:

    Hello Matt & Shartrina , I had found this site via of your aunt Phyllis , now you may have figures out by may name I am your 2nd cousin of which we haven’t see each other for probably 35 years or more. I am very sorry that you’ve had to endure this disease, but I have heard you have been a fighter & have found that special person , “YOUR WIFE” to assist you in helping with your needs . You have proven that there are some tough cookies in this family , & we will always pray for your needs to be met & that includes a cure.
    With Love from Michigan
    Mitch, Kelly, Ashley, Megan, Aryn, Andrew,
    & from Indiana Adam & Julie ,
    see there is alot of “we’s” to help


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