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LDN and MRI (Janet)

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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

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