Guest guest Posted July 5, 2004 Report Share Posted July 5, 2004 Janet, I have not had an MRI since starting LDN. As a matter of fact, other than the initial diagnosis process 15 years ago, and one other one 4 years ago, I'ts never been my focus as I am too busy thinking about how to manage my illness, my job, my home, relationships etc. I am PPMS. I will be visiting my Neuro for the first time in 2 years this September, - my mission? LDN awarness and to show my progress diary and the wonderful results. My Neuro is keeps her ear to the ground for MS research news and is open to experimenting with combinations and alternatives. I agree the MRI's are the only way they can monitor lesion loads, size, and atrophy and I will be interested to see if my Neuro thinks my new results on LDN will warrant an MRI for further investigation. I'm sure others here will respond as to their MRI history before and after LDN as I have seen posts about this topic before. Good luck Friday > I need to hear some positive tories to renew my faith in LDN. Has > anyone had an MRI since starting the LDN?? Curious, Janet Quote Link to comment Share on other sites More sharing options...
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