Guest guest Posted September 1, 2009 Report Share Posted September 1, 2009 I would like to unsubscribe to this link. It does not apply to me. I joined thinking it might help me but I will not benefit from this information. God bless you and I will pray for you all. Re: [low dose naltrexone] an update on what's been happening with me: Art, I'm sorry you're having a hard time lately. Hang in there! God bless. Patty .. In a message dated 8/30/2009 11:23:18 P.M. Eastern Daylight Time, rtee54 writes: an update on what's been happening with me:walking very poor. had two IV steroid (solumedrol) treatments about two weeks ago due to a long term exacerbation i've been going through. so far i don't see any improvement. tried the high dose antioxidant course as prescribed by Dr. Lawrence but it didn't have the desired effect.also restarted Copaxone even though i am not a big fan of the stuff.supposedly Copaxone is okay to use along with LDN.still continue LDN and in fact have increased my dosage varying it between 5 - 7 mgs every night at 10pm. take a 4.5mg capsule and the rest is liquid LDN. this is MY experiment and do NOT recommend it for anyone. i am basing this increase on what Elaine and Dr. Zagon have written as they have said up to 10mgs is safe and effective. i will find out on my own figuring i am an extra large person and maybe need more LDN in my system.i have reduced drastically the intake of vitamins and supplements i was taking. easier on the wallet and maybe less is better. wasn't reaping any obvious benefit swallowing tons of pills and capsules.have added dairy products back into my diet and use 2% milk in a protein shake i consume in the afternoon as a 'pick me up'. i get this protein powder at the Vitamin Shoppe. very tasty and would like to add a few pounds to my frame. have also added red meat back into my diet and so far there is no adverse effects noted. may gradually add wheat back in but so far continue with a gluten free diet. sugar and soy will stay on my forbidden list.i am going to physical therapy for the herniated discs in my back. consists mostly of stretching and i am not optimistic about the results. really need some sort of pain management program.i am still a big supporter of LDN but realizing it is not a cure for my problem. i am thinking because i am a male MS hits us a bit harder than it does females and i am falling into this category. i am a fighter and will continue doing so. ArtMy MS/LDN Story 1988 -2009http://preview.tinyurl.com/cv2gbu Quote Link to comment Share on other sites More sharing options...
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