ALS For support and discussion of Amyotrophic lateral sclerosis (ALS), also referred to as "Lou Gehrig's Disease." In memory of BobbyB.

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 08-28-2008, 07:10 AM #11
BobbyB's Avatar
BobbyB BobbyB is offline
In Remembrance
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
BobbyB BobbyB is offline
In Remembrance
BobbyB's Avatar
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
Heart

Hackney family thanks WL community
Brian Hackney died last week after two-year battle with ALS that brought more than 60 community
By Nicole DeCosta

The West Linn Tidings, Aug 28, 2008


STAFF FILE PHOTO / Vern Uyetake / West Linn Tidings

West Linn resident Brian Hackney is shown here in his West Linn home in January. Hackney suffered from ALS and died on Aug. 15 at the age of 51.



Grace.

Love.

Laughter.

Dignity.

Those are the four words Julie Hackney wrote to describe her late husband Brian Hackney after he died from complications from ALS on Aug. 15. He was 51.

The Web site where she posted these comments – www.bhackney.com – was created so friends, family and community members could stay informed of the West Linn resident’s two-year battle with the disease.

And Brian often used voice recognition software and an adapted computer to post journal entries to the site as he lost his mobility.

About 60 people helped the Hackneys – meals, fund-raising, yard work – as Brian’s condition progressed, saying that ALS didn’t spell out a dreadful disease, but rather “Alltogether. Love. And Support.”

Hackney’s sister, Diane Diamantis of Florida, helped with public relations surrounding the many community fund-raisers for Brian.

She said that from Brian’s disease she has learned, “that not enough people really know what it is or what it is like.”

ALS – Amyotrophic lateral sclerosis – is a neurodegenerative disease that causes motor neurons to die, eliminating the ability of the brain to initiate and control muscle movement.

The condition was first brought to international attention in 1939 when baseball great Lou Gehrig retired from the sport after being diagnosed with ALS.

Brian – a father to two teen-age daughters who was born in Georgia and later moved to Oregon – told those around him that he wanted to have “no bad days.”

“Instead of having the attitude that you are dying from ALS, you are living with ALS,” he told the Tidings in a January 2008 interview.

And Diamantis said everyone Brian encountered picked up on his generosity and positive attitude.

“Everyone I came in contact with,” she said, “made a point to tell me what a wonderful person he was, always smiling – a southern gentleman.”

Diamantis said that Brian was patient to the end, even through frustrating communication efforts that made it difficult for others to understand him.

“He kept a twinkle in his eye, and while he still could communicate – a wry sense of humor,” she said.

Those close to Brian described him as a “helper” and very loyal. Earlier this year, Brian’s longtime friend Ken Keating of SW Portland described Brian’s situation as “the caregiver now (needing) care.”

Through their Web site last week, Julie and her daughters, Megan and Paige, said they’d like to thank everyone for their thoughts, prayers and support for the past two years.

They wrote, “It has made a difficult journey easier know we had a community behind us.

“Brian will continue to live in all our lives. He has touched a community that will forever be changed.”



http://www.westlinntidings.com/news/...86454686435100
__________________

.

ALS/MND Registry

.
BobbyB is offline   Reply With QuoteReply With Quote
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
In Remembrance of BobbyB Paul Wicks ALS 29 12-19-2010 11:53 AM
Remembrance Day Hockey Social Chat 0 11-11-2009 08:09 AM
In remembrance of my Grandmother Brokenfriend ALS 1 12-16-2008 09:05 AM


All times are GMT -5. The time now is 08:36 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.