Dear Dr. Roberts;
Here is my testimonial. When I first wrote to you I felt like a fish swimming in a fishbowl, all alone with my EDS pain and chronic illness. I was ready to try anything and at the point of giving up.
Just a few of my conditions were;
- bulging/herniated C4,C5,and C6
- Ruptured L-5 L6-S1 with tears between 5 and 6
- torn meniscus in left knee
- Right carotid dissection intra and extracranial w/psuedoanerysm under skull and in neck (still there and caused constant, excrutiating pain) 4mm at last MRA
- skins tears easily, bruising horrendous
- joints pop everytime I move – I sound like rice krispies
I was diagnosed with a variant form of EDS in ’04 as my skin cell biopsy showed it wasn’t VEDS.
The meds I was on: Plavix 75 once daily, aspirin 81mg, Toprol 100 mg, Lisinopril 10 mg, Catapres .1 twice daily, flexeril 5 mg once, zanaflex 4 mg once, Celexa 60 mg once, Lipitor 40 mg., Phenerghan 25 mg PRN, Xanax .25 PRN, Percocet 10 mg PRN (not working anymore I have developed a tolerance), Stadol shot at ER standing order for vasospam and migraine, Vit C 5 grams daily, Niacin, Fish Oil and Flax Seed oil.
I had tried Lyrica but it had terrible side effects causing vertigo and vomiting.
When I first wrote to you the worst pain was in my lower back and my left knee and horrible pain in my neck because of the psuedoanerysm.
I could not stand up straight or move without pain radiating down my left leg and spasms in my back. I had been to PT for the last year with little help as my joints are lax and I can not do many of the exercises without popping.
Despite all the meds and every therapy I remained in extreme pain. I was so tired of the extreme pain that I keep myself isolated at home much of the time. I have a reacher, a walker, and a wheelchair but refuse to get in the chair as I don’t want to lose my mobility.
I have had every kind of “-ologist” there is. I was tired of doctors and felt hopeless. Most of my doctors don’t know much about EDS and can only treat my symptoms, as surgery is not an option for me.
When I saw your site and read the testimonials I became convinced that I had severe inflammation. I wrote you on facebook and you sent me Banjo.
After using Banjo for 4 days the neck pain was GONE! I definitely had more energy. My back pain was better but not gone and my left knee with the torn meniscus would still hurt, but only if I moved it in a certain way.
I felt much better overall and the best part was that I couldn’t feel that my neck felt normal for the first time in 5 years! I had been using narcotics with no relief for almost five years and after just two days of Banjo I quit the narcotics. That is the greatest relief as I was so tired of feeling drugged.
Thanks a million! I am loving the pain free neck and am able to bend knee easier. And thank you for your dedication to pain relief with a non-addictive medication. I am very grateful to have an alternative to narcotics which I hated because of the side-effects.
I believe that God sent you to me through FB.
Respectfully and sincerely submitted,
Mary Dunn
I have ehlers Danlos Syndrome chronic fatigue severe left groin pain taking meds that the side effect are worse than the pain. spent a week in the hospital has anaphalactic reaction to morphine, hyper from steroids did not sleep for three days tortured and no better with out diagnosis of cause of pain.
Feeling helpless, hopeless and unable to tolerate pain much longer.
Karen – If you want to try Banjo (and are in the US) I will send you a two week supply at no charge. All I would ask in return is honest feedback. Within 2 weeks you’ll know if it is helping.
Let me know.
Best wishes, Steve
Dr. Steve
My girlfriend suffers from eds also. She bad pain as of lately . Shes is 25 years old ,and one knee has popped out of place 90 times , she had surgery on it and then had to stay in bed for a year to heal from it . Now coming up strong with lots of pain is the other Knee that needs the same ssurgery . So you can imagine how she feels about that one , a year in bed is no joke . Plus the Eds heal time is way longer then us regular folks have to deal with . I was looking for some kind of alternative to get her on to help stop some of this pain she has. , Right now for the first time in her life she is experiencing the worst thus far, which lead her to get these doctor pain pills and there not helping , they dont focus to the were the pain really is .