Guest guest Posted October 13, 2010 Report Share Posted October 13, 2010 I have taken Serrazimes (33 mg) twice a day for a while and think they help. They are Now bought from iHerb. I plan on still taking them, along with all BBD-recommended supplements and the BBD itself after CCSVI treatment (assuming they find CCSVI Friday week). Great to hear of Sandi's improvements. All the best, Janet To: mscured From: nagra101@... Date: Wed, 13 Oct 2010 21:47:57 +0000 Subject: Serrapeptase.... Hello all, I know some of you have taken Serrapeptase over the years. Can you please give me your thoughts on it and the type/dosage you took. My wife Sandi has had the return of her main symptom (spasms in arms) 2 months post-CCSVI. The spasms do not effect her like before, they come and are painful but once they are over she gets on with it. No pins and needles, no fatigue and no cognitive issues, no balance issues - so we are still optimistic ;-) Now thinking of using proteolytic enzymes so need your thoughts and experiences. Cheers, Pinda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 14, 2010 Report Share Posted October 14, 2010 I've taken serrapeptase off and on for many years. They help my swelling feet. The latest brand that I use is high potency, enteric coated 120,000 SRP by Doctor's Best, also purchased at Iherb. I just ordered from GoodHealthUSA.com, where I originally bought it, buy three get one free. I got SerraEzyme 80,000 iu, enteric coated. Because of the CCSVI video I decided to take it regularly again. I also take serrapeptase twice a day on an empty stomach. I bought some nattokinase as well but it has not yet arrived. > > > I have taken Serrazimes (33 mg) twice a day for a while and think they help. They are Now bought from iHerb. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 15, 2010 Report Share Posted October 15, 2010 Folks, this may be a lose-lose situation. Serrepeptase is enteric coated with HPMCP. The last P stands for phthlates--a known plasticizer and endocrine disrupter. Whilst there are brands of Serrepaptase that are non-enteric coating (i.e., without phthlates), these have less proof of dissolving fibrin and may just be a waste of money. Pick your poisons carefully. These companies want to make $$$$. http://www.metolose.jp/e/pharmaceutical/hpmcp.shtml Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2010 Report Share Posted October 18, 2010 Great. Thanks for the heads up. > > Folks, this may be a lose-lose situation. Serrepeptase is enteric coated with HPMCP. The last P stands for phthlates--a known plasticizer and endocrine disrupter. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 28, 2010 Report Share Posted October 28, 2010 Hi Pinda, That enzyme Serrapeptase is the very enzyme I'm looking at that i believe disolves scar tissue. I'm thinking we need to have a more than one approach. Once the scar tissue is disolving, we need to replace it with new Mylean Shield. We also need to balance the t1 & t2 cells to stop them from munching on the Mylean shield. I believe Colostrum and Epicore can achieve that. Of course every will say....No colostrum....that is dairy...I've seen colostrum work in my husband, and began taking it 4 weeks prior to my first MRI. The MS plaque on my spine was not " active " in late August. The funny thing was....that my only MS symptom originated from that plaque on my spine. I have since been taking a more pure form 4x a day, and the " symptom " continues to decline. I've also started taking Epicore on the advice from a friend to reduce my chance of cold or flu and when I researched it WOW...I was amazed with what I found and began taking it 2x a day instead of 1 and put my hubby on it too. I'm really wanting to find some entity that would be willing to scientifically look at my theory. It excites me that you've been using Serrapeptase....have they found any changes in her MRI's they are willing to share? where in the nation are you located? I am near where Epicore was discovered! I've talked to them once...want to talk again! Let's keep in touch! ette > > Hello all, > > I know some of you have taken Serrapeptase over the years. Can you please give me your thoughts on it and the type/dosage you took. > > My wife Sandi has had the return of her main symptom (spasms in arms) 2 months post-CCSVI. The spasms do not effect her like before, they come and are painful but once they are over she gets on with it. No pins and needles, no fatigue and no cognitive issues, no balance issues - so we are still optimistic ;-) > > Now thinking of using proteolytic enzymes so need your thoughts and experiences. > > Cheers, > > Pinda > Quote Link to comment Share on other sites More sharing options...
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