Fall is in the Air… Kind of

.It’s hard to believe that it’s fall.  The temperatures in Atlanta are still 90+ every day and the humidity is still fairly high.  As much as I want to throw on a pair of jeans and sweater, it’s just not time yet. I cannot wait to go to a pumpkin patch this year.  The boys […]

Music for Megan & Family Fest

. Megan Grace Sheridan is our niece who is living with mitochondrial disease (complex 1). The text below has been directly copied from www.meganshope.org. Megan Grace was born on August 3, 2003. She was diagnosed with Mitochondrial Disease (complex 1) on December 2, 2004, at the age of 16 months. This disease affects those diagnosed […]

Support Music for Megan with Stella & Dot Jewelry

.Have you ever heard of mitochondrial disease?  Can you even say those words without stumbling?  Now is your chance to learn more, support a great cause and attend a fabulous family event. I know you are all super busy with the end of summer and that you have been invited to 101 different types of […]

Awareness for Mitochondrial Disease & UMDF – A SUCCESS!

.What a great night at the Atlanta Braves Game supporting UMDF. It has been raining for a week straight now with very cloudy, grey, icky skies. Well last night was absolutely gorgeous! Around 3pm the rain stopped, the sun came out and the night was as perfect as we could ever have imagined. And now […]

I Need a Favor and You Can Help…

.Now that you know a little about Mitochondrial Disease (remember my post a few months ago?) you can show your support by attending an Atlanta Brave’s game on September 18 at 7:30pm. All you have to do is purchase tickets through UMDF and a portion of your ticket purchase is tax deductible. Why not enjoy […]

Mitochondrial Needs Your Help, Support & Awareness….

.Support Music For Megan & Mito Fest Your support brings…HOPE. ENERGY. LIFE. Saturday, September 26, 2009Wills Park Equestrian Center in Alpharetta, GeorgiaFestival begins 4pm Concert begins 7pmTickets: $25/Family or $10/IndividualLearn More on the Music For Megan website here.

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