Saturday, February 17, 2018
9th Annual Dinner/Silent Auction In Memory of Brittany Wilkinson

March 15th, 6-10pm

Break the Barriers 8555 N. Cedar Ave Fresno CA

Tickets: $25

We would like to dedicate this dinner to the beautiful Michelle Mohan who went to be with Brit this past August.

If you would like to donate any silent auction items, products, or services please contact Linda Wilkinson.

Tickets can be purchased and picked up beforehand with Linda or reserved beforehand and purchased and received at the door on the night of the dinner. We do need to know if you plan on purchasing tickets the day of the dinner so to have a proper head count for food.

Thank you so much for your help with our efforts towards a cure!

Published in Slideshow
Dinner Tickets Tickets: $25.00 Location: Break the Barriers 8555 N. Cedar Ave Fresno, CA Event: Saturday March 15 Time: 6:00PM
Published in Blog
Friday, 22 April 2011 16:12

2nd Anuual Softball Tournament

When:  May 22, 2011

Where: Bicentennial Park (Clovis) on Sunnyside

Cost: $200 per team (Co-ed) minimum 9 players

Registration due by: May 21, 2011

Contact: Linda Wilkinson ~  559-299-1767   or   559-779-1785              

for a team roster and registration

Registration Form


Please join Kim Stephens  (KMPH Great Day) & Cooper Pendergast as they host the 2nd Annual Co-ed Softball Tournament in memoriam of our  

Beloved Brittany Wilkinson.

Published in Blog
Sunday, 27 February 2011 20:37

Senator Boxer names bill after Brittany

Senator Boxer Introduces "The Brittany Wilkinson Mitochondrial Disease Research and Treatment Enhancement Act"

On Thursday, December 10, 2009, Senator Barbara Boxer (D-CA), introduced “The Brittany Wilkinson Mitochondrial Disease Research and Treatment Enhancement Act of 2009”.   Boxer’s senate bill is also known as S. 2858. Three additional U.S. Senators signed on as original co-sponsors for the legislation. They are Richard Durbin (D-IL), John Kerry (D-MA) and Robert P. Casey (D-PA).

Read More @ UMDF

Published in Blog
Tuesday, 15 February 2011 01:07

Happy Valentine's Day

Happy Valentines Day from your new Mito Community wishing you all of the support and hope you like our new website.

Published in Blog
Wednesday, 09 February 2011 01:13

Brittany Wilkinson

A beautiful teenage girl flips her long, chestnut, ringlet-curled ponytail as she lies her head back on fushia-colored pillows propped up on a hospital bed in her living room. Though young in years, her piercing blue eyes reveal an old soul. She begins to tell her story, with the hope of making even one more person aware, but soon dozes off. The five-hour daily Carnitine drip has begun.

Britttany Wilkinson, a freshman at Clovis East High School, has seen and lived through more than most adults in her 14 years of life. She lives every day with a life-threatening illness called mitochondrial disease.

Mitochondria are responsible for producing energy in almost every cell in our bodies. If the mitochodria are defective, the body will not function properly. More than one in 4,000 children in the U.S. will be diagnosed with mitochondrial disease by age 10 annually, and the mortality rate can be up to 50 percent each year.

Symptoms of the mitochondrial disease include, but are not limited to: loss of motor control, muscle weakness and pain, cardiac and liver disease, diabetes, breathing problems, seizures, visual/hearing problems, and developmental delays.

Though she has had medical problems her entire life due to the illness, Brittany was finally diagnosed at age seven with mitochondrial disease.

Because mitochondrial disease is genetic and passed solely through the maternal side, her mother, brother and sister had their DNA tested as well. A shock radiated through the family when they all tested positive. Brittany’s mother, Linda, had no idea she was a carrier.

The pieces of the puzzle meshed, and the family finally had a name to explain all the aches and pains they had felt for years. Among other indicators, they all get easily winded and have joint pain. Her sister, Ashley, recently started on a bi-weekly Carnitine drip. Brittany has a mutation in her DNA, which manifests itself in ways more complicated and severe.

Published in Blog

Help us find a cure.....