Joe & Rami's Home on the Web - Ilsa's Fund    


Links of Interest

Muscular Dystrophy Canada

Families of Spinal Muscular Atrophy (FSMA)

Ilsa's Previous Website
(some links are not active)

Global TV Profile on Ilsa
(Quicktime Requred)

Request for Support Letter

Ilsa Photos


Walk for MDC
June 22nd
Edmonton

Support our Team


Ilsa Mae Research Fund

Total Raised to Date

school fundraisers
Free fund raiser thermometer
to track your fund raising progress




To donate to the fund, click the MDC Logo above, and fill in the appropriate info. Under Fund, choose Research and in the comments box make reference to the Ilsa Mae Research Fund.

Thank-you!

 

 

 



Ilsa Mae
, was an angel. She had an angelic personality, laugh and smile. In her short span of time on this earth, she had earned her wings by bringing a bit of joy to everyone she met. This angel was with us for a limited engagement due to a rare neuromuscular killer, Spinal Muscular Atrophy (SMA).

On May 18, 1998, this little angel arrived. After a few hectic weeks with a new baby, thoughts turned to all she could accomplish. Dad was hoping to watch her excel at golf, baseball and hockey. Mom planned to introduce her to running and tap dancing.

When Ilsa reached the age of four months, this angel was not yet able to lift her head, roll over, or do much more than wiggle her toes, but everyone thought she was just setting her own timetable. At six months, Ilsa was diagnosed with SMA.

Ilsa was not expected to be here for her first birthday. Her first birthday came and went along with here second Christmas. On March 28, 2000 Ilsa passed away peacefully while watching Bear in the Big Blue House, just a few months short of her second Birthday. This little angel endured much in her short life without complaint.

Ilsa, our little angel, continues to touch many people lives as she teaches them how precious life is.

Ilsa's Research Fund

In late 2005, our family and the Environmental Services Association of Alberta (ESAA), through MDC created the ILSA MAE RESEARCH FUND.

This fund has the specific goal of supporting SMA research in Canada. Money raised for Muscular Dystrophy Canada at ESAA Events are donated to this fund.

Since the inception of the fund, nearly $51,000 has been raised and since1998, ESAA Members and the environment industry have raised over $70,000 to support the initiatives of MDC.