Hi Ladies & Gentleman, my name is Karla Torres I am 27 yrs old and I have a rare and debilitating neurological disorder called Complex Regional Pain Syndrome
for short). I myself developed CRPS after the shingles virus attacked my spinal cord. Leaving me with CRPS on exactly 50% of my body, which is my whole right side of my body. From my right ear down, splitting my body in half. Unfortanelty I am unable to walk normal anymore because my spinal nerves are so damaged from not being able to find a lasting treatment. There is no official cure for this illness. Only experiments and drugs, and I just don't want to waste my life away like this. I used to be a very active person, worked hard, surfed, I have even been skydiving. I dont want to be disabled I want to be normal and live my life without any restricitons. I have researched and found a new type of treatment called Calamare therapy. A technologically advanced solution for chronic pain management. This device has been shown to be highly effective in the treatment of chemotherapy induced peripheral neuropathy (CIPN), drug-resistant chronic neuropathic and cancer pain, having long-lasting effects.I have read stories of people who have gotten so much relief that it lasted over a YEAR!
I just want to remember what it is like to walk again, run, hug the people I love and just for once not think of pain consuming my life. I have gone from churchs to schools spreading CRPS awareness because this month is NERVEMBER
and all the awareness made maybe a cure will come from it. All I as is for help to live again, and even if you cannot donate a prayer goes a long way as well! Thank you for taking time to read and learn about an illness that millions suffer in silence with.
Thank you & God Bless
Here is also the link to see for yourself how Calamare works http://www.calmarett.com
PS feel free to follow me on instagram @kmt72
facebook page: Living With CRPSlivingwithcrps1.blogspot.com