Parkinson's Disease Tulip


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Old 07-10-2008, 04:55 PM #1
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Default Consider the possible implications

There have been a number of weird reports about PD and the hunt for a cure. Amgen, of course. Years of insisting it was all about ldopa when it was known otherwise. Olanow's patent grab on mucuna that serves as a fine lid on further research. Olanow's resignation from a top position at the same time as the Mother Jones piece on the $3M received from the industry his research was supporting. And, as the "Death in Edmonds" thread revealed, a retraction of a paper that would be ludicrous were it not so sinister.

So what the heck is going on? Here is a theory for the more paranoid of you. You know who you are. Don't we?

PD is intimately connected to dopamine circuitry. That is, in turn, integral to the reward system of the brain. Sex. Gambling. Cocaine. All work through the reward system.

What if it is known that anything that fixes PD will also fix the damaged circuitry that causes people to engage in those other activities? We have pondered the huge sums we generate for BigPharma but that is a speck on the planet compared to those others. If that is true, we will never see a cure my friends.
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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Old 07-10-2008, 06:27 PM #2
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Rick, as you know, I truly believe you're onto something - and it's not just cuz we're brain damaged or on drugs. () Between Monsanto, General Foods, our own top neurology specialists, the insurers and the pharmaceutical companies - these alone - their methods are worse than bombs.

When I met with my own neurologist this week, I said to my doc and two other neurologists who were sitting in on the session, "No one is really working on a cure, are they?" My doctor said, "No. They're not. They're making too much money the way it is." With that, I gave him a hug and said well, I'm going to have to be taking care of myself pretty much then.....

Onward. Or underground. Or whatever. I intend to live and live better than they ever thought I could. He asked me to walk down the hall for them. I walked down the long hall and felt like I was on a runway...click-click, click-click, turned and looked back at their three small faces as the doctors stood there watching me. I walked back, perfectly, shrugged, and my doctor whispered to the others, "18 years.... " It feels really energizing to take the reigns of your own life, whenever you can, however you can....Nobody has a say over your own personal life energy.
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Old 07-10-2008, 09:21 PM #3
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Fiona and Rick, you are definitely in the thick of it now. I have been reading and truly appreciating yours and many others'
contributions. If you see it elsewhere don't be surprised. Rick, you are a strategist with your own style. It takes courage to say how you feel - but so few can for whatever reasons - of course I'm paranoid; but i'll just use it to agitiate and idealize. - is no one else....lol

Fiona - your article about the "deal" between some of the most successful researchers really made me kinda sick.

pipeline has some good summary and analysis coming about all canceled treatments. It may also make you kinda sick.

I think we might just be hearing more about these types of business deals, that I'm sure were thought to be well deserved and incredibly fortunate of them to be sought after.

So much to do....

paula
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Old 07-11-2008, 12:42 AM #4
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Default drug therapy

Use of Ibogaine/Ibocaine to increase GDNF in alcoholism ---and thus a BIG potential for PD could be included in this thread. The timeline in the text of a conference on Ibogaine I am currently reading includes the date the FDA determined further study on Ibocaine was useless--there is a note that there were several pharmaceutical executives who were at this meeting and "helped" the FDA reach this conclusion. Ibogaine is banned in the US and Britian--though used in Spain, Mexico, Belgium, and in many island countries for addiction. reputed to have cured Eric Clapton and Keith Richards of their addictions.
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Old 07-11-2008, 01:53 AM #5
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Default Parkinson's

Quote:
Originally Posted by olsen View Post
Use of Ibogaine/Ibocaine to increase GDNF in alcoholism ---and thus a BIG potential for PD could be included in this thread. The timeline in the text of a conference on Ibogaine I am currently reading includes the date the FDA determined further study on Ibocaine was useless--there is a note that there were several pharmaceutical executives who were at this meeting and "helped" the FDA reach this conclusion. Ibogaine is banned in the US and Britian--though used in Spain, Mexico, Belgium, and in many island countries for addiction. reputed to have cured Eric Clapton and Keith Richards of their addictions.
Thank you for your information, I am not up on all of this. I'm newly diagnosed with PD - the only thing that worked for me was the Neupro patch, which they have recalled. Been trying different meds, nothing helps with tremors. I keep hoping the Michael J Fox's Foundation's funding will bring assistance/cure - unfortunately, I may not see in my life time, but hope my children will see a cure.

Sharon
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Old 07-11-2008, 09:56 AM #6
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Rick,

I came to this conclusion ages ago. There's no incentive for a cure if Big Pharma can keep the cash cow alive. They have way too much money/power so they can control any study and possible cure from ever making its way through the FDA. If anything, they'll find other uses for the same drugs so they can expand their profit base more, i.e. Mirapex and Requip for RLS, etc.

John
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Old 07-11-2008, 01:00 PM #7
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Default to add to the paranoia

I wrote a reply to Rick's this morning which had several points and it would not go through. I sent it again, and again, would not go through. There were no links to websites, no copyright issues, nothing, so my paranoia is making me think big brother or perhaps something else is keeping if from going through? Anyone ever had this happen, and if so, how did you resolve it?

If this post goes through, and my one from this morning didn't, then I'll REALLY be paranoid!

Where do those posts that won't go through get routed? Anyway to get it back from cyberspace?
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Old 07-11-2008, 01:06 PM #8
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Quote:
Originally Posted by lurkingforacure View Post
I wrote a reply to Rick's this morning which had several points and it would not go through. I sent it again, and again, would not go through. There were no links to websites, no copyright issues, nothing, so my paranoia is making me think big brother or perhaps something else is keeping if from going through? Anyone ever had this happen, and if so, how did you resolve it?

If this post goes through, and my one from this morning didn't, then I'll REALLY be paranoid!

Where do those posts that won't go through get routed? Anyway to get it back from cyberspace?
slow browsers cause this. the page times out before it is posted.

make sure you clear your cache and your cookies often. closing other programs helps, so does not having too many windows open.

they just go poof. try typing a reply on a word document or notepad, then just copying and pasting if you keep having this problem.

when i was on dial up, this happened many times. very frustrating. i'm sorry it happened to you. pm me if you need any help.
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Old 07-11-2008, 01:58 PM #9
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Default third time's a charm...

and here's the gist of the first message I sent earlier, the one that got snagged, twice.

Not to be the nay-sayer, but I am not sure Rick is right. Although it does appear that big pharma has no interest in cures, inasmuch as I have not seen one in my lifetime, yet, and that is despite the millions, and billions, of research done, for cancer, AIDS, diabetes, fill in the blank with the "disease" (they even are drugging young children now and migrating them onto a drug-dependent regime for life, unconscionable). And no cure for anything, at least that I know of.

But there will have to be a cure. As more and more people move from being tax-payers to benefits-receivers because of disability (for PD, MS, AIDS, whatever) things will have to change, if only from a pure mathmatical standpoint. Our society is simply not sustainable unless the majority of people in it are paying ample taxes to support it. And I don't see those taxes going down anytime soon, if ever!

As for the point about a connection between a cure for PD and vice, we should keep in mind that the vast majority of gamblers in Vegas (and folks watching the porn in their hotel room) are not compulsive, in that they are able to stop themselves. Thankfully, the vast, vast majority of those same folks also do not have PD. There is much more involved with PD, as researchers are now finally acknowledging, and therefore I don't think a cure for addiction will necessarily equate with a cure for PD. Research from one may help shed insights into the other, but I don't see "one cure fits all" in this case, simply because of the complex nature of PD.

Besides, more and more people are turning away from traditional medicine in favor of alternative treatments that work better than the drugs, for them. Just look at this forum, where so many are trying alternatives, and this is only one forum, for one condition. There are many, many others where people are educating themselves (no doctor is going to do that!) and taking charge of their own health. Communities are seeking to DE-flouridate their water (the first town in the US to flouridate water is now considering taking it back out-big news up north), parents are no longer slathering their innocent kids with sunscreen, more parents are choosing to delay vaccinating their kids, or not vaccinate at all, in all aspects people are learning how to be healthy and AWAY from hospitals, doctors, and drugs. With more and more folks taking charge of their own health, that is bound to yield additional insights into how we all function, with and without PD.

And, my favorite thought in all of this: for every pill that someone passes up in favor of a non-Rx alternative, there goes several dollars off big pharma's bottom line. Think this is not making an increasingly significant difference to that bottom line? Even as I type this there is a strong movement to regulate the vitamin and supplement industry, just as the Rx industry is. Just think, clinical trials for Vitamin C! If you want to have to get a prescription so you can take mucuna, or milk thistle, or ginseng, don't bother contacting your congressman to let him/her know how outraged by this proposal you are. But I digress...

Then there's the greed, both a blessing and a curse (ever notice how "curse" is spelled the same as "cure" but without the "s"?). Just as we feel big pharma's insatiable greed drives it to find only treatments and not cures, milking those treatments until the patent expires, then finally repackaging the same old drug for "new" uses, there are scores of companies waiting in the wings to get in on all of that lucrative disease action. They are the ones coming up with the gene therapies, the DBS, and whatever else is in our future. They are highly competitive, focused in on the goal, and skilled enough to achieve it. We just have to stay as healthy as possible until they do.

I would love to see a charity, to be formed, the sole purpose of which is to pay for the expenses (hospital, travel, meals, lodging, etc.) of a parkie who is unable to pay for a treatment which would get him back on his feet. I fancy it would function like the Heifer organization (google it if you don't know), where someone who received its benefit would then, once he got on his feet again, contribute to the charity so that a fellow parkie could be helped. This would be particularly appropriate if there were a treatment (in or outside the US) that was not approved by the FDA or covered by insurance (for those lucky enough to have it) or medicare/medicaide. This would free parkies from the limitations of only FDA/insurance-approved treatments, and if the charity were big enough, it would encourage researchers to look for solutions outside the confines of the "FDA approved only" box. And, for every person who got back on their feet, and off the meds, that would be one less person sustaining Big Pharma, and as more and more people got on their feet and off the meds, then one day, perhaps Big Pharma just might not be so big anymore...

Last edited by lurkingforacure; 07-11-2008 at 02:02 PM. Reason: missed the word!
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Old 07-11-2008, 02:13 PM #10
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Default just one example

Suppose, just suppose, that in some lab somewhere there is a pill. This pill will do two things. It will eliminate PD symptoms by unblocking some hypothetical dopamine relationship. The other effect - from the same source - is it will eliminate the ability to get high from cocaine. The first effect eliminates a one billion dollar market controlled by BigPharma. But the other eliminates a 500 billion dollar market controlled by the most powerful men on the planet. That pill will never see the light of day. Hypothetically of course. (Hmmm. Odd. Don't see many black helicopters around here....)
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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