MW Foundation

MW Foundation

Mats and Erik

Join UsThank you to everyone for being a part of WOW and the MW foundation. If you would like to donate at any time please call WOW at 787-438-4263 or email us at mwfoundation@wilanderonwheels.com.

Save It, Send It, Share It

Wilander On Wheels is happy to announce the launch of the MW Foundation.

Title Inaugural MW foundation Event as featured on Tennis Channel Aug 27, 2013. To attend next year’s event please contact WOW for details.

SAVE IT SEND IT SHARE IT are the ideals that the MW foundation stands for….not only while on a tennis court….but for every day life. Email the MW Foundation.

The MW Foundation’s main purpose is to help raise awareness for the genetic disease Epidermal Bulluyosa, commonly referred to as EB. EB is a rare genetic connective tissue disorder. There are many genetic and symptomatic variations of EB, but all share the prominent symptom of extremely fragile skin that blisters and tears from minor friction or trauma. Internal organs and bodily systems can also be seriously affected by the disease. EB is always painful, is often pervasive and debilitating, and is in some cases lethal before the age of 30. EB affects 1 out of every 20,000 live births and those born with it are often called ‘Butterfly Children’ because as the analogy goes, their skin is as fragile as the wings of a butterfly. There is no treatment or cure. Daily wound care, pain management and protective bandaging are the only options available. Learn more at debra.org

Mats’ 15 year old son Erik inherited a mild form of this genetic disease at birth. The Wilander’s moved to Sun Valley nearly 12 years ago to help Erik cope with his disorder. Because of Sun Valley’s elevation and lack of humidity, Erik’s skin does not drastically blister. This allows Erik the opportunity to participate in sports and lead a relatively normal life. However, those who have the most severe cases of EB cannot treat their condition with a change of environment.

Currently DEBRA of America is the one and only organization helping to raise awareness for this disease and spearheading the fight to find a cure. Because the majority of treatment is preventative, the organization receives very little funding from the government.The Dystrophic Epidermolysis Bullosa Research Association of America was founded in 1980 and is the only national nonprofit dedicated to funding research for treatments and a cure, while providing supportive services and programs for those who suffer from the rare and painful genetic disorder, “Epidermolysis Bullosa (EB) – The Worst Disease You’ve Never Heard Of.™”

Mats has served as the face of DEBRA for the last 15 years. In an effort to help raise awareness for this organization, WOW is happy to announce the conception of the MW foundation working under the umbrella of DEBRA. The MW foundation hosted its first event at WestSide Tennis Club in Flushing NY last August 27th 2013 during the US Open. More than 100 attendees played with past and current pros such as Mats himself, Jonas Bjorkman, Thomas Johansson, Karel Novacek, David Graham and Cameron Lickle. This will be an annual event and if interested in attending next years event please contact us at mwfoundation@wilanderonwheels.com.

MOTTO
SAVE IT WOW’s motto while on a court practicing. We at WOW believe that you must save every ball hit in your direction. Learn from unorthodox shots and positions. Don’t ever let a moment pass on a court where your greatest effort has not been given. Do not stop play merely because your opponent has hit an out shot. Push yourself as far as your body will allow . . . and then push some more.

SEND IT WOW’s motto while on a tennis court. We at WOW believe you must always take risks but only those that are calculated and with a purpose. When you do this, you send it! By sending it you show confidence in yourself while taking control of your own destiny. If you never send it, you haven’t taken your shot.

SHARE IT Never should you not share your unique gifts with the world. If you are able to contribute and be a giver rather than a taker your life serves a beautiful purpose. By sharing and contributing to the happiness of others you fuel your own soul.

These mottos are not only for the tennis court but can be parlayed to everyday life. Tennis, through fair play, competition, respect for the game and ones opponent, can help give a person the tools to become a better person, and in the end, that is what life is all about . . . being a good person and contributing to the world.

Join Us and Support The MW Foundation

If you would like to make a direct donation please make donation to MW Foundation and send to

Direct Donations
MW Foundation
ATTN: Debra of America
75 Broad Street Suite 300
New York, NY 10004

Wire Transfer Information
Domestic Wires
Receiving Bank: JP Morgan Chase
Lincoln Building-621
60 East 42nd Street
Routing Number: 021000021
Account Number: 2975692372
Beneficiary – MW Foundation
Tax ID: 11-2519726 (debra’s tax id)

INTERNATIONAL SWIFT CODE: CHASUS33

Packages in support of the MW foundation:

Come hit with us prior to the commencement of matches at the Australian Open, French Open, and US Open, sit in WOW’s box seats and be our guest for the day/days/week . . . whatever you would like. Find Out More

Mats currently serves as a tv commentator for EUROSPORT at all four Majors where he hosts a daily highlight show of the tournament days activities entitled Game Set Mats. Addiitonally, he hosts his own show entitled Mats Point where Mats provides insights and a behind-the-scenes look at many of the tournaments outside of the Four Majors. He and WOW would like to invite you as our guests.


Shop to Support DEBRA