The Hoppe ALS Awareness Group
The Hoppe ALS Awareness Group This site is run by Brea, Kassi and April. Feel free to write us with any questions you might have! One of us will be sure to get back with you asap! Thanks!

Female
32 years old
Richmond, Virginia
United States



Last Login: 11/26/2009
Mood: sad Mood Image
View My: Pics | Gifts

   Contacting The Hoppe ALS Awareness Group

 MySpace URL: 

    The Hoppe ALS Awareness Group's Interests
General
ALS LINKS TO WHERE YOU CAN DONATE AND/OR VOLUNTEER

http://www. whatkindofworlddoyouwant.com

http://www.alsa.org/

http://www.projectals.org/

http://www.alsmndalliance.org/

http://www.alshopefoundation.org/

http://www.p2w4l.org/

MusicShow your support by ordering your ALS Stamps!!! Click the picture below to check it out!

Movies

Indestructible trailer
http://www.youtube.com/watch?v=hrU0i9TW8KU

This is for my mama, Linda Hoppe. I love you!!!

Television
HeroesEveryone who is showing their support by helping us spread awareness for ALS. Anyone and everyone who is either suffering from ALS or knows someone who is. Be strong, our thoughts and prayers are with you.

     The Hoppe ALS Awareness Group's Details
Status:Single
Here for:Networking
Zodiac Sign:Leo



The Hoppe ALS Awareness Group R.I.P Linda Posted at 5:57 PM Feb 28
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The Hoppe ALS Awareness Group's Latest Blog Entry  [Subscribe to this Blog]

Indestructible trailer  (view more)

ALS AWARENESS STAMP!!  (view more)

"What kind of world do you want?"  (view more)

THE HOPPE VAN FUND....  (view more)

ALS 'Never Give Up' wristbands...  (view more)

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   The Hoppe ALS Awareness Group's Blurbs
About me:

A message from Brea:

On February 28th, 2009, my mom, Linda Hoppe, lost her battle with ALS. She was diagnosed on March 5th, 2007 and stayed incredibly strong over the past 2 years. As many of you know, and for the ones that don't, my mom had a smile that could light up a room. She was a wonderful friend, mother and wife. She always knew what to say... giving encouragement to move forward... comforting you when you were down... or saying the funniest things to make you laugh so hard your crying and nearly wetting yourself! No matter what it was, somehow, she made everything ok! Most of you already know what ALS is, but for those that do not... ALS is a neuromuscular disease that quickly deteriorates the muscles taking away every bit of independence you have. There is a 2-5 year life span after diagnosis and it is 100% fatal. While your body is completely incapable of doing things for itself, your brain is not affected. The ALS Association--DC/MD/VA Chapter has been amazing to us through this short but ever so long journey. Through the help of your donations, my mom was able to receive free patient care, including equipment from the loan closet and transportation to and from appointments. Last year, with supporters help, the Chapter was able to: donate more than $290,000 to ALS research, purchase and repair $50,000 worth of medical equipment for the loan closet, provide $35,000 in transportation grants to local families, provide $50,000 in respite care grants to local families and serve 200 PALS (patients w/ALS) through Assisted Technology/Augmentative Communication Program. I am proud to say that our team alone raised over $10,000!!! Thank you so much! If you are in the Richmond are, Come out and walk for a cause!! For more information, check out our personal Walk to DeFeat ALS page by clicking the banner below!!! In honor of my mother, we are still going strong and accepting any donations and support to keep the fight against ALS strong so we can stop families from losing their loved ones to this awful disease.

Thanks so much for your support!!!

Who I'd like to meet:
Anyone and everyone who wants to help support our cause to find a cure and defeat ALS!

If you would like to keep up with Linda's progress, please click her "Patients like me" webpage here:

PatientsLikeMe member lindagail

You can show your support by adding this banner to your page!!

ADD THIS BANNER TO YOUR PAGE BY COPYING THE CODE ABOVE!


   The Hoppe ALS Awareness Group's Friend Space (Top 34)
The Hoppe ALS Awareness Group has 1674 friends.
 Linda 


 Brea, Luca & Maris 


 april 


 ~Kas~ 


 Hawesome Hawes in the land of Hawesopolis! 


 sammysnakes 


 kristin 


 Liz Liz 


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 Ron vs. ALS 


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 NEVER GIVE UP ~ ALS *Lou Gehrig's Disease* 


 STEM CELLS = hope 


 Chef-to-the-mac 


 Tom 





The Hoppe ALS Awareness Group's Friends Comments
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Dec 19 2009 5:38 AM

Christmas Comments
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