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


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 12-07-2006, 10:17 PM #1
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
Default 'So much' is powerful look at ALS

'So much' is powerful look at ALS

By Jeff Vice
Deseret Morning News

SO MUCH SO FAST — *** 1/2 — Documentary feature about Lou Gehrig's disease research; not rated, probable PG-13 (drugs, profanity, vulgarity).
The documentary "So Much So Fast" quite clearly shows how much we still don't know about amyotrophic lateral sclerosis, better known as Lou Gehrig's disease.
But it's not just a film about the frustrations of medical science. "So much" is also a very compelling human story.
The film also gains some power with the realization that its main subject, Stephen Heywood, died last month after suffering for years from symptoms caused by the degenerative, neuromuscular disorder.


West City FilmsStephen Heywood holds his son, Alex, in "So Much So Fast." As a result, it's a very strong follow-up to the Oscar-nominated 1996 documentary "Troublesome Creek" for filmmakers Steven Ascher and Jeanne Jordan, who had their own personal experience with ALS when Jordan's mother, Mary Jane, died from the disease.
"So Much" profiles Heywood, a designer and builder who refused to surrender to despair after being diagnosed with ALS, a so-called "orphan disease" (one that affects fewer than a million people, and as a consequence receives less funding from pharmaceutical companies).
And neither does Stephen's older brother Jamie, who quit his job as an engineer to start his own nonprofit research facility, with a staff working tirelessly to discover a cure — or at least develop drugs that will prolong the lives of ALS sufferers.
The film is quite effective as it traces the physical toll the disease takes on Stephen. Footage shows him regress over time as he walks without aid at first — only to end up using a walker and then a wheelchair, and then, though still lively, becomes bedridden.
Almost as heartbreaking is the toll it takes on Jamie, whose marriage and career are both threatened by his efforts to aid his brother. You have to admire Ascher and Jordan's restraint in dealing with the brothers' personal lives, though that subject matter is broached here as well.
"So Much So Fast" is not rated but would probably receive a PG-13 for drug content (use and discussion of various pharmaceuticals) and some frank sexual language (including profanity and crude slang terms). Running time: 87 minutes.
http://deseretnews.com/dn/view/0,1249,650213224,00.html
__________________

.

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
Powerful Fox Ad Puts Focus on Embryonic Stem Cell Research Howardh Parkinson's Disease 6 10-28-2006 06:54 PM


All times are GMT -5. The time now is 07:54 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.