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


advertisement
Reply
 
Thread Tools Display Modes
Old 12-04-2006, 07:54 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 Dying nurse forced to wait for vital help

Dying nurse forced to wait for vital help

A nurse who has dedicated her life to caring for others is now a prisoner in her own home as she dies of a muscle wasting disease.

Lynda Forde, 60, of Howick Park Avenue, Penwortham, has been diagnosed with a rapid form of Motor Neurone Disease, a progressive fatal condition which leads to weakness and wasting of muscles.

Lynda, who has worked for the NHS for more than 40 years, is now completely wheelchair bound, her speech has become slurred and she has problems swallowing.

She is currently confined to a downstairs room in her home and is forced to use a chemical toilet near her kitchen and wash herself in a washing up bowl.

She desperately needs modifications to her home so she can have a living area downstairs, but South Ribble Council has to deal with requests in date order and cannot look at Lynda's case until April at the earliest – but this may be too late.

Lynda's daughter, Louise Craven, today blasted authorities for letting down her mother after a life spent caring for others.

Louise, 36, said: "My mum wants to have what little bit of independence she can before it is taken away from her. It is all about quality of life and dignity and she is being stripped of this.

"I think it is disgusting that she has helped people all her life and now, when she is in a position where she needs help, she is not getting it."

Coun Brenda Wilson, of South Ribble Council, said: "Mrs Ford's situation, like every case we deal with, is a tragic one.

"Unfortunately the demand for disabled facilities grants far outweighs the resources we have in place to meet that demand."

04 December 2006http://www.lep.co.uk/ViewArticle2.aspx?SectionID=73&ArticleID=1911973
__________________

.

ALS/MND Registry

.
BobbyB is offline   Reply With QuoteReply With Quote

advertisement
Reply


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
as told by a critical care nurse -part 1 of the must read lou_lou Parkinson's Disease 1 11-05-2006 12:48 AM
Someday i will be forced to quit forums altogether dyslimbic Bipolar Disorder 9 10-21-2006 06:28 PM
OT, old nurse giving her Mom a shot doydie Multiple Sclerosis 6 09-13-2006 10:52 PM
Nurse worked for ALS awareness BobbyB ALS News & Research 0 09-04-2006 06:12 PM


All times are GMT -5. The time now is 03:25 PM.

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.