Living With Brain Cancer / Glioblastoma Multiforme

Never Give up Hope

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Video from Portland Relay for Life, July 16, 2011. Ted is the tall guy leading the pack on the left holding the banner.  This is his fifth year with a GBM.  Two other team mates can be seen in the video.  Ben is easy to spot because he is pushing his twins and Mike is our team captain.  He is patting Ben on the back.  Both have different forms of brain cancer, but are 6 year plus survivors.  
 
 
To see our orginal site go to the link below.  We discuss surgery, chemo and radiation treatments. 

      https://sites.google.com/site/glioblastomamultiforme/

Photos below were taken on December 14, 2010, 4 years and 6 months past Ted's diagnosis, at Translational Genomics Research Institute (TGen) in Phoenix, AZ.    I want to get the word out about the great work they are doing and how GBM patients might benefit from their current research. I am standing next to Ted in the first two pictures.  The last photo in the line is of my parents, me, Ted,  Brandy and Candice. Candice and Brandy treated us like VIPs as we toured the T-GEN facility and learned what we can do for brain cancer research.   

Below are pictures of Ted's 25 year reunion at Washington University School of Physical Therapy in St. Louis.  We had a great time as usual.  These picture were taken Oct. 21-25, 2010, 4 years and 4 months past his GBM diagnosis.  He's the tall guy in the back. The second shot was taken at an urban sculpture park in St. Louis.  Ted and I are looking through a giant head.  No sign of tumors. The third picture was taken at a happy hour with former classmates. 

BELOW PHOTOS WERE FROM Ted's 4 YEAR SURVIVOR BIRTHDAY PARTY

Ted's four year anniversary party on May 30, 2010.  There was way too much good food!  We dodged raindrops.  The hearty Pacific "Northwesterners" held strong and withstood the rain, while many of the former Californians retreated inside for a brief time.  Overall, it only rained for about 20 minutes; just in time to eat of course.  We had 25 guests. There were three other brain cancer survivors at the party.  The first photo is of Ben, Jennifer, Ted and Deana.  All four are brain cancer survivors.  Ben was diagnosed in 2005, Jennifer in Sept. 2007, Ted on Memorial Day 2006 and Deana in 2004 for the second time.  She was diagnosed ten years before but has successfully beaten it both times.    

 

 Ben, Jennifer, Ted and Deana: all brain cancer survivors.  Ben enjoying a burger while his wife Ann gets in line.

 

Food line.  Caron, Ann and Ted                                  Ann, Les and me (Ann and Les teach with me)

 

 Ardie, Stanley(the hairy one), Char, and Patrick                      Caron, Ann, Char and Ted                                                       

                        

Great shot of my back!  Chris is in the back, I'm                   Gloria, her husband Les and Luanne.  The party was

talking to Randy and Gloria, and Ardie is trying to                held at Luanne's house.  She has a great yard for a party,

find the sun.                                                                                       and she's an all around great person.   Thanks Luanne.

     

Ted and I.  My what big flowers!  Very fattening cake, but my intentions were good. 

 

Jennifer, Ted, Deana, Andre, Rich, and Margaret.       Ann and Caron enjoying the refreshments. 

 

  

To see our original website with photos and information about surgery, radiation and chemo go to:

https://sites.google.com/site/glioblastomamultiforme/

 This site is to give hope to those newly diagnosed with a GBM.  My husband Ted was diagnosed in May of 2006.  After seeing only horribly depressing websites about GBMs, I decided we should create our own site to give people hope.  I update Ted's MRI results immediately upon hearing the news.  Check the Health Update for the latest.  
 
 
In July of 2009 we visited The Brain Tumor Center in San Francisco. The doctor told us that cancer should NOW be looked at as a chronic illness that can be treated instead of naturally assuming that everyone is doomed as soon as they get the diagnosis. I appreciated the attitude!      
 
 
     
 Photo number 1: Ted's 56th Birthday on Feb. 13, 2009.  Photo number 2: Our athletic trainers, Morgan and Silvi.  Photo number 3 the latest addition to our training team.  We adopted her December 24, 2009 from a shelter in Arizona.  What a great dog.  She came already trained.   Silvi, the cute little schnauzer in the middle picture, and Ted's shadow, passed away Sept. 9, 2011.  My heart still breaks for the little one.  She was 16 and a half years old.  
 
 


  
HAPPY HOUR
Photo taken Feb. 6, 2010.  Katy, Ted, Jennifer, and Chris.  Jennifer is also a GBM survivor.  She was diagnosed in Oct. 2007. 
 
 

 We have a new addition to our pack!  We adopted KC on our last trip to Arizona.  She had been found wandering around a Circle K store with her puppy.  Her pup was adopted right away, so we took the little love bug in and made her the newest member of our fitness club.

 Do you know how tough it is to get three furballs to pose in one shot?  One day, we will get it right.  Silvi is on the left, Morgan in the middle and part of KC on the lower corner.  I'll try again next week!