Guest guest Posted February 1, 2008 Report Share Posted February 1, 2008 I am about to go to my neurologist,after a recent MRI that shows new lesions and having what are being referred to as ms hugs and having various other problems including slurring and balance problems and more most of which started after I started taking the copaxone which I want to stop so badly It depresses me to think I will have to have a shot every day for the rest of my life and its not even going that good I take it last thing before I go to bed and then it takes 1-2 hours of laying in pain until I can finally fall asleep, so I am going to beg and plead with him to ok me to start taking LDN and even tho we are living unemployed right now, (my hubby just got laid off from his job great timing right) I will pay for it if my ins wont, so my reason for telling you all this is if you are taking LDN and it has changed you life please write about it and send it to me via email to mommyangel96@... ,knowing that I'm askng your permission to print and share your story. I want as much compelling info as I can get and what better place than not only professional opinions, but most important other users, Thank you to anyone who can do this and please now how much I truely appreciate it. I'll keep you all updated as to what happens I don't actually have the appt yet but it will be no more than two weeks so I have a lot of work to do before than concerning this any help to research or anything you may think will be helpful would be much appreciated also. Thank you, Quote Link to comment Share on other sites More sharing options...
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