Excuse me if this is inappropriate, ahem!
My dad gave me the idea and told me to come online and see what you guys thought of it. All of you seem SO resourceful so I will just ask...
Does the MS Society help out with patients who have a probable diagnosis of MS, who lost their jobs and health insurance and only need a few more tests to help confirm things? As in, will the MS medical centers fund these tests to help someone out? Like continue where other doctors left off to help get a diagnosis? Or at least rule MS in or out altogether?
Thank you in advance if you have advice.
My dad gave me the idea and told me to come online and see what you guys thought of it. All of you seem SO resourceful so I will just ask...
Does the MS Society help out with patients who have a probable diagnosis of MS, who lost their jobs and health insurance and only need a few more tests to help confirm things? As in, will the MS medical centers fund these tests to help someone out? Like continue where other doctors left off to help get a diagnosis? Or at least rule MS in or out altogether?
Thank you in advance if you have advice.
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