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Is Anyone Here Seeing A Neurologist?

Is Anyone Here Seeing A Neurologist?

I can't seem to find a decent Rheumy that cares or takes my insurance. I've done a lot of research and some say you should see a neurologist.

A MyFibroTeam Member said:

A rheumi diagnosed me, but it wasn't until I saw a pain management doctor and his team of other specialists that I learned to manage alot of my pain. I would try that.

posted almost 7 years ago
A MyFibroTeam Member said:

waw you LO)L L0

posted over 6 years ago
A MyFibroTeam Member said:

Same here. I started out at the Neurologist and he referred me to my rheumatologist. Once my doctor figured out that I don't complain, when I tell you I hurt, I HURT and I follow directions almost literally we get along really well. I am one of his few patients that do well on an old cocktail. I am in a bit of a flare up, but am fighting to keep moving. The pain slows me down.

posted almost 7 years ago
A MyFibroTeam Member said:

@New member. I saw a neurologist he did nothing for me. He sent me to a rheumatologist and he has helped me lots more. I probably depends on the dr.((hugs))

posted almost 7 years ago
A MyFibroTeam Member said:

I see a neurologist x2 yearly but thats for my narcolepsy and cataplexy . Next time i see him im going to ask about this MS thing .

posted over 2 years ago
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