Kind of worried
 

Not such a good visit to the neuro today. Having alot of problems and neuro thinks it may be the MS progressing. I have alot of tests to go thru, without insurance, and possibly more steroids. Prayers are very much welcomed if you wouldnt mind.

Prayer gladly offered up

You got 'em :smileypray::smileypray:!!

Good wishes through your tests.:hug:

Gladly given & good luck to you. If I might ask; have you found anywhere in TN to help you? I used to live in East TN (Newport & Del Rio).

I am praying for you that you are not progressing. Could the MS Society help you in any way?

Prayers being said for you. Please let us know how the testing goes.:hug::hug:

prayers and hopes being sent. Try not to worry before you have to, it could also just be a particluarly rough patch. Regardless, we are still here for you!:grouphug:

Best vibes headed your way for good results! :)

Are you having to pay full fare for these tests? Is there a university hospital near you that might run the tests? Generally they offer programs with big discounts for uninsured.

Thinking of you and have everything crossed for a good outcome. Good luck with the tests - hoping that nothing too scary pops up.

Regards

Lyn xx

There are better days ahead of you. Try not to worry too much. You are in my prayers.

MSAA is providing a free MRI of the brain. Neuro really wants a spinal MRI, but they dont pay for that, so that will have to wait.

My neuro has cut his bill down by over 200.00 a visit. He is constantly trying to do things that is within my budget even down to the meds he gives me. He is great and I couldnt ask for a better neuro. I have applied for a few other things with the MSAA and Im still currently waiting for replies.

Yes, we have to pay for everything execept the MRI out of pocket. My dh cant sign up for insurance until February. I will be making alot of calls to my surrounding hospitals and ask for prices on the bloodtests. We live close to a university hospital, and they will be one of the hospitals that I will be calling.

I used to work for a teaching hospital and one way we could get around getting care for a patient was that the exam, xray, cardia cath, etc had to be used for teaching purposes. So the residents had to watch. Now granted that was a lot of years ago but that may be one thing you could ask about.

When I lived in Natchez Miss., I drove almost 2 hours to Jackson to the University Medical Center, which had a great MS clinic. That's where I was diagnosed. No insurance at all. I paid 10% for everything except a couple of specialists who poked their head in the door:rolleyes:. And yes, there were always students present.

The only irritation I experienced in my time there (almost 2 years) was that I did not have "a" neuro who followed me exclusively. But the care was good.

I suggest calling the facility where you will have the testing done and ask for the department that handles "Charitable Care applications". If you do not get an effective response call the Administration dept.

I hope you can get what you need and not go broke doing it. Life on a limited income is hard.