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Old 03-14-2011, 12:30 PM #1
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Angry I am P***ED!

I guess I'm going to Die with MS. Big Pharma have no intention of showing us a cure until they've bled us dry of all our wordly goods, first. That probably means, we will all die with MS.

Not that MS will cause our death, just that it will be our companion in death, just as is is in life.

Where do we protest this unfairness? To whom do we complain? From where will we get truthful answers? Aren't you a little P***ED?
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Old 03-14-2011, 01:14 PM #2
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It's probably not in Big Pharma's "best interest financially" to offer us something that would either cure it or otherwise keep us from having to depend on some sort of med. It's all about the big bucks. Makes me mad, too.
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Old 03-14-2011, 01:22 PM #3
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Yes, but I want answers, Kell. I want someone to have the guts to come forward and tell me that I am wrong or right, in my assumption and what they intend to do about it.

The only way that big pharms is going to come up with something that really works is to stop taking the meds that aren't working.
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Old 03-14-2011, 02:19 PM #4
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Quote:
Originally Posted by SallyC View Post
The only way that big pharms is going to come up with something that really works is to stop taking the meds that aren't working.
Well, I've done my part........... None of the meds they've offered so far have done me any good.
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Old 03-14-2011, 03:23 PM #5
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I've stopped taking anything for my MS. Including the baclofen. I'm now using exercise, physical therapy, and beating up the Mii characters in my Wii, as a way to deal with spasticity. (I really enjoy beating on the Mii characters in the sword fighting game)

Now the only medications that I take are the occasional migraine pill and some Tylenol or ibuprofen.

I'm still wobbly walking a bit, but not as bad as I had been. I had a really good day friday. Went to PT, and when I walked in, I was carrying my cane, twirling it like a baton, and did great on most of my exercises. Today I'll be dragging myself in there, but at least friday I was able to walk nearly normally.

My neuro kind of ruined any faith I had in any of the MS meds when he told me once that he didnt think any of the injectibles worked. That was just before I quit stabbing myself with the C. (I pretty much quit it that night) At least he told me the truth about his personal opinion of the stabby drugs. (he's a very old neuro and is a bit old school. Doesnt order MRI's every time there's a change. He can figure out where my problems are coming from by my telling him what's not working right)
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Old 03-14-2011, 06:14 PM #6
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I try (not usually successfully) to avoid being angry. Some people can channel anger well, God bless 'em. My daughter, for example, can get her dander up and use it constructively. She becomes more articulate, more determined, more energized.

Me, not so much. If I let myself get really p.o.'d, it tends to spiral out of control, and I just end up with a stomachache and humongous anxiety. I totally agree with you, though.
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Old 03-26-2011, 09:11 AM #7
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Default Hi Sally

Sorry you have ms. My cousin does too. I think the drug companies could do alot more. Too much money is wasted. I was bled dry financially also. I believe science has the tools to do alot more than they do. I know there are studies out there for ms. Do you want to enter a trial of some kind? I just hope you will get some kind of better help soon. ginnie
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