Guest guest Posted March 22, 2011 Report Share Posted March 22, 2011 Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. My feet would scrape and drag on the ground, I could barely move my legs. They felt heavy and weak. I didn't have the strength to stand for very long. My balance was so bad I needed a nordic pole and my husbands arm. I couldn't turn my head and walk as I would tip over and loose my balance. My arms were getting heavy. My feet were numb which I wasn't aware of until after starting the prokarin I realized I could feel the carpet fibers scratching on my feet. My legs felt like logs that were connected to my hips. It was so hard to walk and move. The spasity was so severe when I stood it would travel from my legs up to my back and down my arms to my fingers which would curl backwards. I would shake at times from the ms making my muscles quiver. I was in lots of pain from the ms. My neck hurt from the inflammation there. Now I can walk normally without a cane. I can turn my head walking. I can get up at night without having to hold on to furniture to balance. My thoughs are clearer. My fingers can type better. I can tip toe, jog in the house, jump. I feel really good on the prokarin. It has done more for me than any other product out there including LDN. I am extremely impressed with the change. I felt like I was at the end of my rope before that my time was limited before I would be in a wheelchair or totally housebound due to the severity of the symptoms I have. Now I have my life back. I can exercise again and go for walks. My foot drop is almost gone. Its still there but its greatly improved. It takes time for the body to repair itself. My muscles still fatigue easily but each day there is improvement in the distance I can walk. Yesterday I went to the post office and two stores and did very well without assistance or a cane. I was able to turn my head and look around without falling.  ________________________________ To: " mscured " <mscured > Cc: " lowdosenaltrexone " <lowdosenaltrexone > Sent: Tue, March 22, 2011 9:35:11 AM Subject: Re: Re: [lowdosenaltrexone] New Member -need your help!  hi rachael - quite agree that is why i said that everybody is different with varying results  good for you and pleased worked so quick  stay tuned  regards peter  'they say ldn is long term fix so why does anybody expect to take this after a couple of weeks and inspect to see improvements is beyond me,' I am then the odd one out I'm afraid . I had my nightly (all-night generally) tearful, excruciating and searing left leg muscular pain struggles erased by LDN after only about a week. *shrugs* 'i have copied in an email group called 'mscured' has there been anybody cured?' That's a good one ! lol I don't believe that anyone has been 'cured' as such, but I'm pretty sure that we are doing a heck of a lot better than others who aren't open to the 'alternative' treatments discussed and used by the members here. 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2011 Report Share Posted March 22, 2011 Wow Joy. What an amazing and quick turnaround. Congratulations. Where did you get the Prokarin? ________________________________ To: mscured Sent: Tue, March 22, 2011 1:50:56 PM Subject: Re: Re Prokarin Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2011 Report Share Posted March 22, 2011 I got it from the pharmacy in washington state. They custom make it for you. I am astonished at the change in my ability to move. Today I went on a 2.5 mile walk with my husband. I did it all by myself unaided other than a nordic pole. I felt like it would be best on a long walk to keep it handy still as I feel at times as my body is still relearning how to walk right. If you know what i mean. I did call out for my husband once when I had a balance issue other than that I did great. I normally have to cling to him when I walk. Especially down hill as my leg tends to buckle. Today it was strong and did not feel the need to buckle. When I walked up a steep hill my muscles all engaged so I walked up well, better than before. The last time I did it, I had to stop and rest several times and I struggled the whole way. Today my pace was brisk maybe 3.5 mph or so through the whole walk. A week ago I could barely walk. I was able to turn my head and look around as I walk. Normally I have to hold my head still because moving it or my eyes would make me dizzy. I could walk and look around at the wildlife. It was great.  I did fine when we went out to best buy and another store walking around without the nordic pole, but I also felt kind of like I missed it. Like in a way it still gives me a bit of feed back on my walking. In a way maybe I have become kind of dependent on it in situations like that. I noticed improvement walking the first day. Each day I get better. Now when I get up during the night to pee, I my legs work well. They aren't heavy and they move easily. I don't have to hold the furniture and door frames to balance and help me sit on the toilet. I did kind of force the neuro to give me prokarin. He did not want to prescribe it. I had asked 6 months ago and he refused. I told him the definition of insanity is doing the same thing over and over again and expecting different results. That I was going downhill and loosing my ability to walk and move my arms. He did not want me to go off the regular meds. He doesn't know I did. He said prokarin wouldn't work. I said I don't care. even if it gives me a placibo effect and I benefit from it I want to try it. He said get it over the counter. I said I need a prescription. He turned red when he wrote it out and did it very reluctantly. He said there is no proof It works. I said back in the 1940 a doc from mayo clinic was giving it in IVs to pts. with MS. It worked better than steroids for decreasing inflammation and causing symptoms to go away. He was blown away that I knew that. I said Look its an amino acid its harmless so give me the prescription. If it doesn't work it doesn't work. I want to try it. Research has shown it reduced inflammation and helps with remyelination. Some companies are doing research to use it for parkinson's patients in the form of betahistamine a h3 agonist. It helps with the shaking, alertness, mood, enegry, mental clarity. My speech is not slurred anymore. It used to slur 8 or more times a day. My face would droop like a stroke patient. It doesn't anymore. People with ms are low in histamine according to research. Its a neurotransmitter that helps get the messages to the muscles. The patch is helping to replace the histamine that you are low on. There are 4 different forms of histamine. h1, h2, h3, h4. H1 is the one that causes allergies. H2 is the one in prokarin which helps with the nerves. H3 also helps with nerves and is in betahistamine. I am trying to lean this stuff as I want to see improvement. I was so fusterated. I think I would of been classified as seconday progressive with the severe symptoms I had. I was so close to being totally wheelchair dependent. I don't know if this helps. Do the research. Type in h1,h2,h3, h4 receptors MS, neurology, meylin, neuropathways, etc. to try to find links. Read pattents out there. They are using the h3 for cancer treatment. I am wondering it may be a future LDN type thing for MS. A little know treatment that helps. Oh, today I started sweating. I could barely sweat before. I think that is good right ??? ________________________________ To: mscured Sent: Tue, March 22, 2011 11:37:45 AM Subject: Re: Re Prokarin  Wow Joy. What an amazing and quick turnaround. Congratulations. Where did you get the Prokarin? ________________________________ To: mscured Sent: Tue, March 22, 2011 1:50:56 PM Subject: Re: Re Prokarin  Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 where can you source prokarin in in uk ? regards peter To: mscured Sent: Tuesday, 22 March 2011, 18:37 Subject: Re: Re Prokarin  Wow Joy. What an amazing and quick turnaround. Congratulations. Where did you get the Prokarin? ________________________________ To: mscured Sent: Tue, March 22, 2011 1:50:56 PM Subject: Re: Re Prokarin  Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 Hi all I've started my search for UK Prokarin here on Facebook with this group. I'll keep up the search but wil use the suggestions given by those that know a bit more than I do about the whole thng. It does sound worthwhile to give it a try (still being mindful of side effects for athsmatics though) that's for sure! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured CC: lowdosenaltrexone From: peter.nicholls@... Date: Wed, 23 Mar 2011 09:51:48 +0000 Subject: Re: Re Prokarin where can you source prokarin in in uk ? regards peter Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 And in Spain or can it be mail-ordered? Janet To: mscured CC: lowdosenaltrexone From: peter.nicholls@... Date: Wed, 23 Mar 2011 09:51:48 +0000 Subject: Re: Re Prokarin where can you source prokarin in in uk ? regards peter To: mscured Sent: Tuesday, 22 March 2011, 18:37 Subject: Re: Re Prokarin Wow Joy. What an amazing and quick turnaround. Congratulations. Where did you get the Prokarin? ________________________________ To: mscured Sent: Tue, March 22, 2011 1:50:56 PM Subject: Re: Re Prokarin Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 Well done Joy, that is great news! I remember people here mentioning Prokarin in the past. Is anyone else still on it and what benefits have you seen? Although I've had CCSVI treatment, my balance and mobility haven't altered a lot but everything else has just vanished so the combination could be the key. Janet To: mscured From: yourbeamofsunshine@... Date: Tue, 22 Mar 2011 17:28:03 -0700 Subject: Re: Re Prokarin I got it from the pharmacy in washington state. They custom make it for you. I am astonished at the change in my ability to move. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 They say you have to be careful if you have ashma on the inserts. ________________________________ To: MSCured <mscured > Sent: Wed, March 23, 2011 5:30:18 AM Subject: RE: Re Prokarin  Hi all I've started my search for UK Prokarin here on Facebook with this group. I'll keep up the search but wil use the suggestions given by those that know a bit more than I do about the whole thng. It does sound worthwhile to give it a try (still being mindful of side effects for athsmatics though) that's for sure! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured CC: lowdosenaltrexone From: peter.nicholls@... Date: Wed, 23 Mar 2011 09:51:48 +0000 Subject: Re: Re Prokarin where can you source prokarin in in uk ? regards peter Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 Yep - that was one of the first things I read when searching for its details. I'm an athsmatic so must be very careful of anything like this - antihistamines have the same warnings. Nothing has ever happened and they've never caused me problems, but I'm always carefully aware of the 'risks'. I'll be going ahead when I find where is best for me to get it from here in the UK. I'm so happy for your improvements Joy! It's just terriffic!! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 06:20:37 -0700 Subject: Re: Re Prokarin They say you have to be careful if you have ashma on the inserts. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 You need a doctor's perscription. The uk ms website has instructions how to make it. The problem is I don't know where to get the supplies. They said it can be made for a fraction of the price of the patch. That would be the ulitmate thing. http://edmsllc.com/ http://aeholland.com/prokarindrinfo.pdf http://allnurses.com/general-nursing-discussion/prokarin-ms-patients-49814.html http://www.msrc.co.uk/index.cfm/fuseaction/show/pageid/1872 http://www.direct-ms.org/pdf/DrugsMS/TransdermalHistamine.pdf http://www.bioportfolio.com/resources/pmarticle/102630/Histamine-In-The-Cns-Mult\ iple-Functions-And-Potential-Neurologic-Implications.html There is a website out there by a guy named goodkind who had a wife with ms who he made patches from the raw ingredients with instructions how to make it. His wife passed years ago so the site is not updated. She also had heart problems I believe which was the cause of death. There are many sites out there that have infor. But you need to put in a search for h2 or h2 receptors agonist and multiple sclerosis into the search engine. I am wondering about betahistamine as its a h3 receptor agonist and it is used for menigers disease. According to some patent sites they have tested it for parkinsons disease, weight loss, mood improvement, enegry, cognitive function, etc. The company was merk and a few other that were researching the use. However they were probably going to rename it. I am not an expert, I am reading trying to make sence of what has been researched and how it affects. They said it helps with cancer also. That is why I was wondering if it might be in the same league as LDN in the future??? Yesterday I was able to walk 2.25 miles briskly as It started raining. I did use a cane just in case as I don't want to fall. I only grabbed my husband once because of a brief loss of balance when I was looking around. I stll feel like my senses are overloaded when walking and there are a bunch of people who walk up. It has made me feel the sensation like I can't balance. But yesterday it wasn't as bad. I walked uphill without slowing down and resting. Normally I have to stop and rest. I picked something off the floor without having to worry about tipping over. It was like old times before ms. In the evening I did a barre dvd which really focuses on strengthening the quads and glutes, hips all the muscles that are weak from ms. It has helped more than any other workout due to the movements. It looks easy but is very hard due to pulses of movments while holding the muscles tight. Its very controlled yet I don't overheat while doing it. I don't know if its just my time in life to have hot flashes or its the med? I am 48. The last two nights I have woken up with hot flashes. I know I am in the time range. I have had other symptoms. I did not enjoy the hot flashes and waking up sticky and sweaty. Maybe its because since I started taking prokarin I can now sweat when I exercise where as before I hardly sweated. ________________________________ To: " mscured " <mscured > Cc: " lowdosenaltrexone " <lowdosenaltrexone > Sent: Wed, March 23, 2011 2:51:48 AM Subject: Re: Re Prokarin  where can you source prokarin in in uk ? regards peter To: mscured Sent: Tuesday, 22 March 2011, 18:37 Subject: Re: Re Prokarin  Wow Joy. What an amazing and quick turnaround. Congratulations. Where did you get the Prokarin? ________________________________ To: mscured Sent: Tue, March 22, 2011 1:50:56 PM Subject: Re: Re Prokarin  Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 http://www.sparkpeople.com/mypage_public_journal_individual.asp?blog_id=4103493 My embarrasing journal. I have been tracking symptoms of ms and me trying to loose weight. I have written about prokarin there. ________________________________ To: MS-Cured <mscured > Sent: Wed, March 23, 2011 5:38:36 AM Subject: RE: Re Prokarin  Well done Joy, that is great news! I remember people here mentioning Prokarin in the past. Is anyone else still on it and what benefits have you seen? Although I've had CCSVI treatment, my balance and mobility haven't altered a lot but everything else has just vanished so the combination could be the key. Janet To: mscured From: yourbeamofsunshine@... Date: Tue, 22 Mar 2011 17:28:03 -0700 Subject: Re: Re Prokarin I got it from the pharmacy in washington state. They custom make it for you. I am astonished at the change in my ability to move. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 Thank you I am thrilled. I just pray it lasts. I worry about the costs of it. My only income is such a small amount. Now if the creative genius of the group can figure out a way for me to afford it by making an inexpensive version I would be sooo happy. I never expected to have this kind of improvement. I can tap my fingers together fast. I havent been able to do that in years. I showed my husband. I was about 1/3 the speed of him finger movement wise. Catching a ball was hard due to slow reflexes. Two weeks ago I was about ready to give up and give in to the wheelcair in the garage. Then prokarin hit. I was shopping online for a walker. LOL. That is how bad my condition was. I am still getting the burning neuropathy in my right foot but its less intense. I hope it fixes it. I hate the burning pain. ________________________________ To: MSCured <mscured > Sent: Wed, March 23, 2011 6:26:05 AM Subject: RE: Re Prokarin  Yep - that was one of the first things I read when searching for its details. I'm an athsmatic so must be very careful of anything like this - antihistamines have the same warnings. Nothing has ever happened and they've never caused me problems, but I'm always carefully aware of the 'risks'. I'll be going ahead when I find where is best for me to get it from here in the UK. I'm so happy for your improvements Joy! It's just terriffic!! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 06:20:37 -0700 Subject: Re: Re Prokarin They say you have to be careful if you have ashma on the inserts. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 Still researching Prokarin on here. So far I've tracked down a pharmacy in Toronto (?) who will ship it to you in Europe (no mention of cost though). But you need a prescription and as I've just had a run in with my neuro over his non-belief in CCSVI I can't see how I could get one. I can't find the way to make it up yourself, anyone have the link? Janet To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 07:15:38 -0700 Subject: Re: Re Prokarin Thank you I am thrilled. I just pray it lasts. I worry about the costs of it. My only income is such a small amount. Now if the creative genius of the group can figure out a way for me to afford it by making an inexpensive version I would be sooo happy. I never expected to have this kind of improvement. I can tap my fingers together fast. I havent been able to do that in years. I showed my husband. I was about 1/3 the speed of him finger movement wise. Catching a ball was hard due to slow reflexes. Two weeks ago I was about ready to give up and give in to the wheelcair in the garage. Then prokarin hit. I was shopping online for a walker. LOL. That is how bad my condition was. I am still getting the burning neuropathy in my right foot but its less intense. I hope it fixes it. I hate the burning pain. ________________________________ To: MSCured <mscured > Sent: Wed, March 23, 2011 6:26:05 AM Subject: RE: Re Prokarin Yep - that was one of the first things I read when searching for its details. I'm an athsmatic so must be very careful of anything like this - antihistamines have the same warnings. Nothing has ever happened and they've never caused me problems, but I'm always carefully aware of the 'risks'. I'll be going ahead when I find where is best for me to get it from here in the UK. I'm so happy for your improvements Joy! It's just terriffic!! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 06:20:37 -0700 Subject: Re: Re Prokarin They say you have to be careful if you have ashma on the inserts. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 ah yes! the eternal fight against the extra bits of ourselves which gather becaue we can't walk etc! I'm fighting to lose weight at the moment too! I've started using the whole calorie-count website (http://caloriecount.about.com) which logs my weight, what I eat and my exercise too! It's quite good. The BBD has never had me losing weight, I've put it on over the time that I was immobile. I'm just hoping to be back in my favourite clothes by the end of Spring! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 06:57:15 -0700 Subject: Re: Re Prokarin http://www.sparkpeople.com/mypage_public_journal_individual.asp?blog_id=4103493 My embarrasing journal. I have been tracking symptoms of ms and me trying to loose weight. I have written about prokarin there. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 I have been using sparkpeople to monitor my calories, exercise, ms symptoms, blog about how I feel. There is a large group of people who have ms there. I believe there are three MS teams who support each other's efforts to loose weight, exercise, and deal with the ups and downs of ms. Its great. Of course there are other groups. I went there because I found support that was positive rather than dwelling on the wo is me attitude and I am never going to get better type stuff that is common to other forums. I wanted to focus on a positive attitude and healing rather than negative thoughts. That is why I am there. It also is a journey of my healing progress. I do it for me, the comments though are nice. ________________________________ To: MSCured <mscured > Sent: Wed, March 23, 2011 7:32:09 AM Subject: RE: Re Prokarin  ah yes! the eternal fight against the extra bits of ourselves which gather becaue we can't walk etc! I'm fighting to lose weight at the moment too! I've started using the whole calorie-count website (http://caloriecount.about.com) which logs my weight, what I eat and my exercise too! It's quite good. The BBD has never had me losing weight, I've put it on over the time that I was immobile. I'm just hoping to be back in my favourite clothes by the end of Spring! 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 06:57:15 -0700 Subject: Re: Re Prokarin http://www.sparkpeople.com/mypage_public_journal_individual.asp?blog_id=4103493 My embarrasing journal. I have been tracking symptoms of ms and me trying to loose weight. I have written about prokarin there. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 Here is one patent that has been filed. If you read up they are using betahistine which works on the h3 receptors to help ms symptoms. It talks about how it works in the patent. It is dry reading but you will see helpful info. http://www.wipo.int/pctdb/en/wo.jsp?wo=2007076140 & IA=US2006049321 & DISPLAY=DESC I don't know if its being tested out. Even then its fusterating to wait years to see if it gets approved. ________________________________ To: mscured Sent: Tue, March 22, 2011 10:50:56 AM Subject: Re: Re Prokarin  Hi, I am on Prokarin and I absolutely love what it is doing for me. Its only day 4 and I have gone from being almost wheelchair bound to walking normally. Before I could walk only about 500 feet with severe difficulty. It took all my strength to walk. My feet would scrape and drag on the ground, I could barely move my legs. They felt heavy and weak. I didn't have the strength to stand for very long. My balance was so bad I needed a nordic pole and my husbands arm. I couldn't turn my head and walk as I would tip over and loose my balance. My arms were getting heavy. My feet were numb which I wasn't aware of until after starting the prokarin I realized I could feel the carpet fibers scratching on my feet. My legs felt like logs that were connected to my hips. It was so hard to walk and move. The spasity was so severe when I stood it would travel from my legs up to my back and down my arms to my fingers which would curl backwards. I would shake at times from the ms making my muscles quiver. I was in lots of pain from the ms. My neck hurt from the inflammation there. Now I can walk normally without a cane. I can turn my head walking. I can get up at night without having to hold on to furniture to balance. My thoughs are clearer. My fingers can type better. I can tip toe, jog in the house, jump. I feel really good on the prokarin. It has done more for me than any other product out there including LDN. I am extremely impressed with the change. I felt like I was at the end of my rope before that my time was limited before I would be in a wheelchair or totally housebound due to the severity of the symptoms I have. Now I have my life back. I can exercise again and go for walks. My foot drop is almost gone. Its still there but its greatly improved. It takes time for the body to repair itself. My muscles still fatigue easily but each day there is improvement in the distance I can walk. Yesterday I went to the post office and two stores and did very well without assistance or a cane. I was able to turn my head and look around without falling.  ________________________________ To: " mscured " <mscured > Cc: " lowdosenaltrexone " <lowdosenaltrexone > Sent: Tue, March 22, 2011 9:35:11 AM Subject: Re: Re: [lowdosenaltrexone] New Member -need your help!  hi rachael - quite agree that is why i said that everybody is different with varying results  good for you and pleased worked so quick  stay tuned  regards peter  'they say ldn is long term fix so why does anybody expect to take this after a couple of weeks and inspect to see improvements is beyond me,' I am then the odd one out I'm afraid . I had my nightly (all-night generally) tearful, excruciating and searing left leg muscular pain struggles erased by LDN after only about a week. *shrugs* 'i have copied in an email group called 'mscured' has there been anybody cured?' That's a good one ! lol I don't believe that anyone has been 'cured' as such, but I'm pretty sure that we are doing a heck of a lot better than others who aren't open to the 'alternative' treatments discussed and used by the members here. 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2011 Report Share Posted March 23, 2011 I asked the Prokarin group on Facebook (Treat MS with Prokarin) about getting it in the UK, and got this reply: ' Yes Prokarin can by shipped to you in the UK. The newest formulation of Prokarin is available as a disc that you simply peel off of a piece of paper and stick in on your skin in the morn...ing and remove it at bedtime. The Prokarin disc doesn't have the skin irritation issues that the Prokarin cream that is applied to a patch can have. The Prokarin disc can be sent to you from the Medicine Shoppe pharmacy in Toronto Ontario Canada as they can accept a prescription from your doctor in the UK. The email contact for the Medicine Shoppe pharmacy is linda@... If you don't have a doctor to prescribe the Prokarin, you can contact Dr. Woeller via email as he will do Skype consultations. His email is info@.... , as for your question regarding athsmatics and Prokarin, we have listed every possible side effect listed by the FDA for the active ingredients in Prokarin. We have people with asthma using the Prokarin and we have not received any reports of problems.' I hope that answers some questions for people - it certainly has for me. 'What we do in life, echoes through eternity.' MARCUS AURELIUS (121 - 180 A.D.) To: mscured From: yourbeamofsunshine@... Date: Wed, 23 Mar 2011 10:42:26 -0700 Subject: Re: Re Prokarin Here is one patent that has been filed. Quote Link to comment Share on other sites More sharing options...
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