Anyone going to Eugene?: Shared Solutions... - My MSAA Community

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Anyone going to Eugene?

greaterexp profile image
greaterexp
β€’8 Replies

Shared Solutions has a program in Eugene, Oregon on March 21 at 6:30 at the Hilton about living with MS. I don't have a link handy, but I'm sure it's easy to find. I'm not sure if it would be worth the expense of the traveling there. Has anyone been to an event of this type?

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greaterexp profile image
greaterexp
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8 Replies
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jkdavid99 profile image
jkdavid99

I live in Eugene but I haven't heard of this. I will look it up and see what I can find. Usually at these things they have speakers and a little dinner. Where are you located at?

greaterexp profile image
greaterexpβ€’ in reply tojkdavid99

Southern Oregon

jkdavid99 profile image
jkdavid99

I just looked it up. My Neuro will be speaking so I may go to see what he says.

Raingrrl profile image
Raingrrl

I saw that it's sponsored by the Copaxone pharma. They also have some in Washington within driving distance for me I wonder how much the discussion will be about Copaxone. I took Copaxone until it stopped working for me so I don't really want to hear a lot about it. Any thoughts about this?

CherieMSCN profile image
CherieMSCN

Try this link: copaxone.com/multiple-scler...

greaterexp profile image
greaterexp

CherieMSCN , thank you for posting the link!

CalfeeChick profile image
CalfeeChickCommunityAmbassador

I have a 5 hr appt. at MS Clinic for nerve conduction tests in spine and optical nerves on the 21st. I think I'd rather go with you 😊

greaterexp profile image
greaterexpβ€’ in reply toCalfeeChick

CalfeeChick , I would, too, were I you, but I'm glad you're getting the tests done to get more answers. I'm not going anyway.

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