Additional Support

I am closing this site down. As of April 2010 I will no longer have this site up and running. It will be available to any who want the domain name. I don't update it and don't want to pay for it anymore. While it's not expensive, it's an expense that I don't want to pay.

Additional Support

I wanted to make this page to make you, my reader, aware of ALL the support options out there for you.

There will be some forums that you post on that you don't feel truly help you, THAT IS O.K. So many people are out there getting the word out about RSD/CRPS and you can always search for another group.

Find one that truly helps YOU. It sounds selfish, but it's your pain, it's your life - FEEL COMFORTABLE, FEEL SECURE - because you will get personal.

Here are a few Personal Stories. If you find more, or have one yourself, please email me and I will put them in here. Of course, my life since my injury is in my blog. Just click on this sentence.

http://www.news.com.au/heraldsun/story/0,21985,23370587-2862,00.html Hopes and Heroes "For months Tim has battled a condition called complex regional pain syndrome."

It is here that I am placing lawsuits won/settled which deal with Complex Regional Pain Syndrome, aka, Reflex Sympathetic Dystrophy. The reason for this is to show you that even the courts acknowledge your pains as being real. Also, if you have an Attorney, you can take from these links and give the information to your lawyer.

1. Settlement Reached

2. My case settled. I had a lawsuit due to my injury. It took a while and a lot of stress but I prevailed in the end. My RSD/CRPS was acknowledged and for that I am grateful. At times I ask myself, and I guess now I ask you, What is the price you would put on the rest of your life? I feel that I am blessed. I have been able to get treatments that people haven't yet considered for RSD/CRPS and have responded more than wonderfully to them.

3. Do you have a link that would go well here? Please share...

www.USARSD.org

www.RSDS.org

www.RSDHope.org

http://www.rsdandyou.com/

here are all the friends I have through MySpace with RSD - just in case you have a MySpace account.

http://friends.myspace.com/index.cfm?fuseaction=user.viewfriends&friendID=50424202&catID=-9223178239290021494&MyToken=926f0070-a876-4fc0-b0c2-7101c9823cd0

http://groups.yahoo.com/group/RSD-CRPSofAmerica/?yguid=336672945

http://www.painfoundation.org/

http://www.painreliefnetwork.org/

http://www.rsds-crps-news.blogspot.com/

http://www.crps-rsd-a-better-life.blogspot.com/

http://www.rsdfoundation.org/

http://capricorn-sister.blogspot.com/

http://neurotalk.psychcentral.com/

http://www.fightingrsd.co.uk/

http://melsreallifedrama.wordpress.com/

http://rsdandyou.com/

http://powerofpain.org/

http://www.ninds.nih.gov/news_and_events/news_articles/news_article_crps.htm

http://crpsrsd.myfastforum.org

http://www.hopeforelizabeth.com/index.html

http://setmattfreeofrsd.com/

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