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Started By
Message
Need neurologist and a MRI place that take cash, not ins
Posted on 9/24/17 at 5:36 pm
Posted on 9/24/17 at 5:36 pm
I am being diagnosed with MS (Multiple Sclerosis). My Dr is a GP and is in New Orleans.I need to find a place in BR that does reasonable priced MRIs for cash (and possible a spinal tap). I also need recs on a good Rheumatologist (correction: neurologist) around BR who is good with MS
If you are anyone you know has MS and can help me find the right Dr and an MRI place I would be very grateful.
I am doing well so far except for the fatigue, passing out, pain, exhaustion and all the other symptoms of MS. In a way I am relieved to finally find out the reason why I have been suffering like this for about a decade.
For so long the unconcerned Drs tried to just play it off as Fibro and I know it was not that. It pissed me off and insulted me. I knew there was something very wring, I had to give up a lucrative career and also give up teaching because I was unable to do the things I love.
I would also be interested if anyone here has MS or knows anyone with MS and their experiences with it.
If you are anyone you know has MS and can help me find the right Dr and an MRI place I would be very grateful.
I am doing well so far except for the fatigue, passing out, pain, exhaustion and all the other symptoms of MS. In a way I am relieved to finally find out the reason why I have been suffering like this for about a decade.
For so long the unconcerned Drs tried to just play it off as Fibro and I know it was not that. It pissed me off and insulted me. I knew there was something very wring, I had to give up a lucrative career and also give up teaching because I was unable to do the things I love.
I would also be interested if anyone here has MS or knows anyone with MS and their experiences with it.
This post was edited on 9/24/17 at 7:50 pm
21
Posted on 9/24/17 at 5:37 pm to gingerkittie
MRI is gonna run you $700 to $1000 for cash price.
Posted on 9/24/17 at 5:38 pm to gingerkittie
I don't have an answer for you, but best of luck with your treatment.
I'm sure there are MRI and Dr's that will do cash and save you a lot of money in the process.
I'm sure there are MRI and Dr's that will do cash and save you a lot of money in the process.
Posted on 9/24/17 at 5:38 pm to gingerkittie
quote:
spinal tap
Sure it's not SC? Spontaneous combustion?
Posted on 9/24/17 at 5:41 pm to gingerkittie
You will need a neurologist, not rheumatologist
A good neurologist will do the lumbar puncture in office
If your neurologist wont do it in office he is lazy and probably incompetent
MRI if you shop around might find under $1000 without contrast, add $500 for contrast
A good neurologist will do the lumbar puncture in office
If your neurologist wont do it in office he is lazy and probably incompetent
MRI if you shop around might find under $1000 without contrast, add $500 for contrast
This post was edited on 9/24/17 at 5:43 pm
Posted on 9/24/17 at 5:41 pm to gingerkittie
I promise you any doctor will gladly take cash. They will probably even give you a discount if you ask.
Posted on 9/24/17 at 5:43 pm to gingerkittie
I can't help you with a Dr referral or insight about living with MS but you're clearly very upset which I understand.
Google MS support groups and message boards. Not only will you find support but you'll eventually key in on some local help there too.
Maybe think about counseling too. You'll get support and guidance on how to handle your new situation.
Google MS support groups and message boards. Not only will you find support but you'll eventually key in on some local help there too.
Maybe think about counseling too. You'll get support and guidance on how to handle your new situation.
Posted on 9/24/17 at 5:44 pm to gingerkittie
How exactly were you diagnosed with no lumbar puncture or MRI?
Posted on 9/24/17 at 5:46 pm to gingerkittie
My mom had it. It caused her to make shite posts on an message board and leave my dad for a cousin
Posted on 9/24/17 at 5:48 pm to gingerkittie
quote:
I am being diagnosed with MS (Multiple Sclerosis).
Sorry to hear that. I'm in need of a Rheumatologist too (for a condition called Polymyalgia Rheumatica) apparently around here it takes months to get in to see one. Good luck to you.
Posted on 9/24/17 at 5:49 pm to gingerkittie
You need a neurologist
You will probably have to pay up front but any office should take cash
My mom has MS, her shot that she takes 3x a week is over 5k a month
You will probably have to pay up front but any office should take cash
My mom has MS, her shot that she takes 3x a week is over 5k a month
Posted on 9/24/17 at 5:50 pm to arkiebrian
Dr. Irving is a good neurologist who specializes in MS. Her office is at Perkins Rowe.
Posted on 9/24/17 at 5:51 pm to arkiebrian
quote:
around here it takes months to get in to see one
Where are you?
Are you are somewhat close to ahreveport?
Posted on 9/24/17 at 5:55 pm to gingerkittie
it would be cheaper to buy an ins policy than to pay cash. *although peoples rates are surreal nowadays with Ocare.
Posted on 9/24/17 at 5:56 pm to gingerkittie
My father has MS... he's been through all kinds of experimental treatment over the last 30 years including 2 rounds of chemo and multiple daily injections of vitamins just to name a few... he does smoke marijuana daily, it helps with the pain and tremors... it has slowed the progression of the disease, but not stopped it... 2 years ago he had a case of the shingles, and that has taken what little energy he had left
I know he goes to the NeuroMedical Center in BR next to Perkins Rowe, and has made multiple trips to Houston to see other specialists
He does physical therapy 3 times a week and it helps his mobility greatly, but after 30 years, he is essentially bedridden
*it is very important to note this disease effects different people in different ways... some people have a harder time with it due to progression and the individual's body, and some people, like my father, have an "easier go" at it... there have been great strides in MS research and care in the past decades*
As for details about insurance, I am not familiar with any, as my step mom handles that side of things
It's a long fight gk, stay strong
I know he goes to the NeuroMedical Center in BR next to Perkins Rowe, and has made multiple trips to Houston to see other specialists
He does physical therapy 3 times a week and it helps his mobility greatly, but after 30 years, he is essentially bedridden
*it is very important to note this disease effects different people in different ways... some people have a harder time with it due to progression and the individual's body, and some people, like my father, have an "easier go" at it... there have been great strides in MS research and care in the past decades*
As for details about insurance, I am not familiar with any, as my step mom handles that side of things
It's a long fight gk, stay strong
Posted on 9/24/17 at 6:12 pm to gingerkittie
I don't have MS, but I have RA. My rheumatologist isn't in BR, either.
But, I can tell you this: I hope you have insurance because all the rheumatology shite ain't cheap.
But, I can tell you this: I hope you have insurance because all the rheumatology shite ain't cheap.
Posted on 9/24/17 at 6:16 pm to HarryBalzack
Guys, stop wasting your time. She hasn't been diagnosed with anything. Just a crazy lady looking for attention.
Posted on 9/24/17 at 6:17 pm to cajunangelle
nice little jab at Obama trumpkin
Posted on 9/24/17 at 6:17 pm to ksayetiger
quote:
I promise you any doctor will gladly take cash. They will probably even give you a discount if you ask.
I completely agree. If OP asks around I think success will be found early in finding someone.
Good luck with everything.
Posted on 9/24/17 at 6:18 pm to Cosmo
quote:
How exactly were you diagnosed with no lumbar puncture or MRI?
I had the MRI long ago (post katrina) and it was just a baseline MRI for Alzheimers testing (runs in my family) and Epilepsy. They were not looking for MS but did see signs of it. Now they cannot find that MRI and want to do a new definitive one that is just for MS. Or that's how it was explained to me.
My GP (of 12 years) knows I have all of the signs and symptoms of it and so he is quite comfy with diagnosing me as such (Presumptive MS?_) as all of the other testing he has done has ruled other causes out. So he feels comfortable with treating me as an MS patient and I have responded well this treatment.
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