The Brooks Family Foundation for RSD/CRPS
After 9 years of pain, Tracy has her life back!  Help us help others get their lives back too!

 

Please leave a note for us!
Showing: 11-15 of 390
Brenda said:   September 8, 2008 10:28 am PST
So glad to find your website -- I have RSD/CRPS and have wanted to do something to help raise awareness. I am still trying to balance my life with this condition and am not ready to actively pursue awareness/research programs, etc., but I so want to help raise awareness. I have had to stifle my anger several times as doctors have discounted my pain.

Tracy Jones said:   September 7, 2008 12:27 pm PST
tracy i have had rsd since 01 i live in oklahoma i am trying to start a support and awareness group here if you have any suggestions please contact me i am to trying to raise money to have the ketamine treatment please look at my webite @freewebs.comoklahomarsdcrpssupport may god bless you, tracy

Val Pepe said:   August 10, 2008 11:17 am PST
I am a single Mom with a daughter who has full body RSD.She has been thru 2 neuro stims lost to hospital infections and now has an intrathecal spinal pain pump which since March has done little to calm her pain.We have been to Mayo etc. Please connect us to Ketamine treatment and possible donations to help us. I have run out of funds and need help badly. She has been in severe pain for nine years!. Please email or call me.

Kathy Donaldson said:   August 4, 2008 7:35 am PST
My daughter has full body RSD and is on the list to go to Germany. Does your foundation give any monies for people who need financial help.

Don said:   May 9, 2008 11:22 am PST
Eric-I have always been impressed with you.Now that I read the web site,I also have utmost admiration for your entire family.Check is in the mail.

Sign My Guestbook
Name:
Email:
Message:
Enter security code:
Verify