Re: HAPPY DAYS WITH HOPE COULD SOON BE HERE!!!!!CONSIDERING TAKING LDN

[Guest guest]

Your story touched my heart and I pray for you and your family. Your words show a person with tremendous courage and strength. Don't ever envision yourself as being a cripple ever again! You can never be a cripple. Noone with strength of mind and spirit can ever dwindle down to that state of being. Forget the physical because it is a temporary condition. You carry your spirit through eternity and that part of you seems to be functioning on a high plane. I wish for you the best with the LDN and attitude plays so much in the success of any treatment. You have a good one so keep being positive. Kathy

[low dose naltrexone] HAPPY DAYS WITH HOPE COULD SOON BE HERE!!!!!CONSIDERING TAKING LDN

I am using this email more as a post!!! I setup what I thought was an appt with my GP today. I got into the examining room to give my presentation on LDN and ask some question about the vaccine.

They tell me he isnt in!!! They tell me Ihave to see his colleague!! My Dr knows me, we r friends, I've never met this guy!!

I EDUCATED THE HELL OUT OF HIM!!!!!! He was amazingly nice and very receptive. He is going to do some rearch tonight just to make sure there is something we are overlooking. When he is impressed(his words), tommorow he will come in first thing in the morning and talk to my DR about it.

He even said that me coming in there with handouts and being so educated and upfront helped. He said" If u asked me to shoot avacado juice in your arm I'd be like -no-. This seems absolutly harmless. Worse case scenario it doesnt work." He asked alot of questions and I answered them all!!

Moral of the story...Dont just rely on your neuro. Go for your other dr's as well. They seem to remember a little easier sometimes people are more than complex nerve bundles and have a soul too.

I should have the RX by this time tomorrow. With there permission I will let you know there names, but I will tell them as well since they are giving me the opporotunity, I am putty in there hands. If they want me to take it for 6 mnths first b4 giving out there names. He did say if it worked on me he wouldnt think twice of doing it again.

Please pray for me people. I'm not a cripple yet but I am heading there and I believe all of you believing in me will help to!!

Chris

mboylebradley <mboylebradley@...> wrote: Hi Pete .. I just read your email from a few days ago. Glad you enjoyed the book.First, this is the right place to talk to people with MS on LDN.Endorphin testing is difficult because they fluctuate daily and fluctuate differently for each person. More research is needed in that whole area. I hope your insurance covers the $500.To persuade your Neuro .. I think the best way is to bring all of the information but he won't believe it, so ask him if he thinks it would do you any harm. Most agree it won't so ask him to humor you for a couple of months. He will think you are crazy but remember you are ahead of the game until he sits you down and recommends intensive psychiatric help. If that happens, agree to counseling after a couple of months on LDN .. To be serious what I would do now without question and hindsight and all that .. I would import from medsmex.com and home brew. It is very simple and will always be right. gave great instructions a day or so ago .. very, very, easy with no aggravation. Tell your Neuro that is what you are going to do if he won't help.Noel just had a full physical after 3 years on LDN .. everything is fine .. liver included. He is very healthy apart from his MS he was told. I never realized male physicals were so intrusive but confess after 3 children my sympathy was lacking.Noel has no side efects. The people I know with RRMS on LDN are all doing great with no side effects bar the first week or so when they had vivid dreams and difficulty sleeping.There are links to the LDN conference .. you can back track this board or maybe Larry will point you in an easier direction because I know he has kept them all somewhere. Larry is very organized. Thanks Larry.All the Best > I was diagnosed with MS in March of 2001. Thankfully symptoms have> been mild and stable and limited to varying degrees of numbness in my> hands. I had no new symptoms until January 2005.> > Since January, the numbness in my hands has increased and I've > experienced slight numbness in my feet. About five weeks ago I had> an episode of optic neuritis in my right eye. I had a steroid> treatment> and the vision is better, but not 100%. I started Copaxone a few> weeks ago. > > I read Bradley's book about LDN book and am amazed and hopeful> as well as a bit skeptical. I would like to present information on> LDN> to my neurologist and suggest this as a treatment option, but I need> to be> prepared with lots of solid information. My neurologist is very> traditional> and without clinical trial evidence, he might be hard to convince.> > I have all the info from low dose naltrexone.org. > > I am interested in e-mailing or speaking directly to people with MS> who are currently taking LDN to find out their experience.> > Is anyone with mild RRMS symptoms currently taking LDN? What is your > experience?> > I would like to know how people have gotten scripts for LDN. From> Dr. Bihari? From your neurologist?> > Has anyone had endorphin level tests before or during their time on> LDN?> > Has anyone on LDN been tested to monitor their liver function?> > Is anyone experiencing side effects major or minor?> > Unfortunately I found out about the LDN conference last week, so I> missed it. I was wondering if there is documentation available from> any of the> speakers.> > If you couid contact me directly, that would be great.> > -Pete

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