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#1
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![]() This is an interesting site and video project on living with MS in Europe. Thanks for the tip, LivWell!
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Dave Bexfield ActiveMSers |
#2
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![]() The MS International Federation was linked to the European Multiple Sclerosis Project (EMSP), which looks to be affiliated with our Ntl MS Society.
After reading through some of the pictures' descriptions, my daydreams of living in Europe have been markedly deflated and I'm a lot more appreciative of our convoluted and occasionally flawed, health care system... and the ADA... and elevators. |
#3
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![]() Very interesting how care varies from country to country. Also very depressing to see those that aren’t getting the care they need.
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#4
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![]() I found it sobering too Grady. It really altered my perspective and makes me wonder if there is any way to advocate for changes. I always thought the health care for PwMS in Europe was at least on a par with ours. From this info, there seem to be real needs at very basic levels.
Local advocacy is good too as there are also needs here in the U.S. Differences in Medicaid/Medicare coverage state to state can have a huge impact on people when they need to relocate. The NMSS is a member of the MS International Federation. Maybe there is an effort already at work. |
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