Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


advertisement
Reply
 
Thread Tools Display Modes
Old 10-11-2012, 06:50 PM #1
Kevscar
Guest
 
Posts: n/a
Kevscar
Guest
 
Posts: n/a
Default The RSD Fighters Anthem

It may seem old fashioned to the younger ones of you but I have always lived by a self-imposed Code of Honour, a sense of duty that you have to help others no matter the cost to yourself. even though they will never know my name.
For 2 years now I have been fighting to get the UK Government to do something to find the un/misdiagnosed in this country and the only help despite thousands of e-mails started 6 months ago by my MP. There have been times when I have been knocked back so badly I have really wanted to give up but one tune and the thought that I want, when I die for my family to be proud that I did everything I could until my last breath.
A couple of months ago I decided I needed to do something more to really drive it home people. While I was trying t work out what I found out that my estimate of 250,000 was probably 200,000 low, that my duty did not stop at the English coastline, there could be over 5 million un/misdiagnosed Americans so around the world 10,s if not 100,s of millions and my duty was just as much to them as UK citizens. That meant a worldwide campaign.
http://www.youtube.com/watch?v=bx0ZCwlm5FY

To make this successful I need you, so if you have a sense of duty, your religion says you should help others, you don't want others to wait as long as you did or get the same bad treatments or you just need something to distract you daily from the pain join me.
If you are willing to be in the video I need before and after portrait photo’s put side by side on a landscape JPG. At the Top of the before "RSD Started DD/MM/YYYY" at the bottom "No. of Spreads" At the Top of the After "RSD Diagnosed DD/MM/YYYY. The bottom you can leave blank, put your name and Location or a short message it.s up to you.
If you can't do this yourself you can send the stuff to me and I will do it for you.
I have set up a special e-mail address just for this RSDFighter@Hotmail.co.uk
  Reply With QuoteReply With Quote

advertisement
Old 10-13-2012, 07:15 PM #2
Kevscar
Guest
 
Posts: n/a
Kevscar
Guest
 
Posts: n/a
Default

I know it sounds strange considering what we have but we are the doubly lucky ones, firstly we have been diagnosed while based on every figure out there 100, of millions across have not.
Secondly only a small proportion have found sites like this where we can give and get support so please spare 5 1/2mins to listen to this and consider helping the unlucky ones

.
http://www.youtube.com/watch?v=bx0ZCwlm5FY
  Reply With QuoteReply With Quote
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
Settlement - Anthem Blue Cross & HealthNet Victor H Multiple Sclerosis 1 02-12-2009 12:00 PM
Anthem trebla Creative Corner 0 02-29-2008 08:37 AM


All times are GMT -5. The time now is 03:38 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.