May 2014
At age 14, Kara was diagnosed with CRPS after surgery for a dislocated kneecap. She spent the next four years undergoing painful, invasive and ultimately unsuccessful pain treatment efforts. By age 18, Kara was wheelchair-bound and living with CRPS symptoms including skin lesions, swelling, discoloration, allodynia and temperature change sensitivity. But her unrelenting father was determined to help his daughter and through his research, discovered Calmare scrambler therapy.
June 1, 2015 at 10:49 am
Dear Liz,
Thank you for reaching out and we are sorry to hear of your daughter’s battle with CRPS. We are very familiar with the situation you have presented and would like to talk with you in more detail specifically about:
*the nature of your daughter’s original injury/surgery
*medications she is using
*other CRPS therapies she has undergone
*her overall health and mobility situation as of today
Please call us her here in NJ or privately email us your phone number at calmarenj at gmail.com or via private Facebook message here: https://www.facebook.com/calmare.nj
We look forward to talking with you.
Sincerely,
Barbara
Calmare Therapy NJ
June 1, 2015 at 10:08 am
Hello, my name is Liz and my 18 year old daughter has had CRPS for 2 years. The doctors at UNC Chapel Hill want to place a spinal cord stimulator in her spine and I wanted to talk to you about your daughter’s experience and history with CRPS. Please feel free to contact me.
Thank you,
Liz Bourgeois