TESTIMONIALS - PAGE 3
I have had MS since 1978. It started with the loss of sight in one eye. The sight returned and the MS disappeared until 1992. My main symptoms are a very weak right leg, feet that are hard & numb with no movement and legs that are cold.
A friend saw a program about Prokarin on Pax TV. My neurologist was hesitant but my family doctor agreed to let me try it. I have been on Prokarin for two months. The first month the numbness in both feet lessened so that I could move toes and get the feeling back. The second month: legs that were cold are now warm all day and feel normal. I do one hour of exercises each day and the legs are much stronger.
If a person has MS they should try Prokarin. The drug is a cream and applied to a patch-no shots and I have experienced no side effects.
C.D.
I was diagnosed with MS in 1980 and since that time have had my ups and downs. In 1990 my doctor said "You have MS" and I asked now what? The response was "We'll keep an eye on it".
In 1993 I fell 8 feet onto my head and it took 9 months to return to work & it was then that my doctor said accidents and sickness are not good for people with MS. I was having 3 or 4 exacerbations per year. He started me on Copaxon-for 3 years I had no help & asked for another drug. He then sent me to an MS doctor in his office complex, who put me on Avonex, again no help.
I knew a man who at that time had been on Prokarin for 4 or so years & he was 68 then. After speaking with him and watching him I felt what he was doing should work for me. I started asking questions and the cost was less than my copay on the other drug plus the pills I took for spasticity and my jerking, which added up all together to over $480 per month, which all came out of my pocket. I contacted Elaine DeLack for more info & she gave me three doctors' names. To start, I spoke to Dr. David Steele, MD in Everett & for the last 20 months I haven't had any exacerbation. Yes, it does take time to get going on Prokarin, but for me it was well worth it.
As I live my life now, I can stay up until 10 PM easy. I have more energy and I'm not so tired in the afternoon. Sure I still have MS, but now it is in my control & as for cost & availability, almost no problem. I get it in one day and out of pocket cost is very manageable for me now. Yes, my insurance doesn't pay, but at least I will not go to the poor house crawling. I walk with a cane or arm crutch & use a scooter for my longer trips. This drug has given me my life back under my control.
Thanks Prokarin.
G.T.
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