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15 months on LDN

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i don't remember if i posted this before so sorry if this is a

double thing. i've been so fried lately. i hope everyone is well.

i got my mris back last month and brain, cervical and thoracic spine

are all stabile. disability however is a pain in the butt. my eyes

were getting better as confirmed by my opthomologist, but i find

that the area that i see clearly( not more than one ) is getting

smaller. i've initiated occupational therapy again starting on the

13th, where the therapist was successful in getting my eyes to

converge before to a point. hopefully it will happen again.

one other worry is that there are many times, mostly when i have

been speaking for 15 minutes or more, that i feel i lack the breath

to get words out anymore and i sound very nasal.

BTW i'd love to hear from anyone who has an idea on how to manage

stress, real life stress effectively. i am trying to handle it but

it is just too much and i am feeling worse everyday. any help would

be appreciated.

also, has anyone heard from anyone who underwent a stem cell

transplant for MS out of the country. the non chemo way lol. from

what i can find to read it seems to be as effective as LDN but for

30k. i'd be interested to hear of any lasting results.

summer is here and laying on the beach is ok right now with the

temps in the low to mid 70's here in the hamptons in NY. i hope

everyone is having a good start to the summer. i want to throw

someone at my local nmss chapter. they know nothing.

all my best,

joanna

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