Parkinson's Disease Tulip


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Old 10-10-2013, 10:11 AM #1
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Default New Trigger of Alzheimer’s Identified: Stress

http://articles.mercola.com/sites/ar...ign=20131010Z1

Presumably, this applies to PD as well. At least it did in my case.
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Old 10-12-2013, 07:35 PM #2
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Default Gerry

Ditto! I have always been a believer of this stress theory.
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Old 10-12-2013, 11:05 PM #3
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Default same

I believe stress causes PD as well, we just don't know the mechanism....does it cause our arteries to become stiff so our brains don't get the blood/oxygen they used to and need...or does the dumping of cortisol put us in a sympathetic nervous system dominance, where we don't/can't rest and repair...all of these or maybe even something else stress causes that we don't yet know, but it definitely figures in there, because while everyone's PD may be different in terms of symptoms, everyone's PD is significantly worsened by stress.
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Old 10-13-2013, 02:53 PM #4
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Default Cocensus!

Lurkingforacure

I believe that this exacerbation of symptoms when stress enters the picture, is one reason why we haven't found better treatments or maybe even a cure. There are no assessment tools that can help level out the playing field enough to cover for the huge variables trial participants experience when stress enters the picture. Remember that stressors can alters brain chemicals greatly, thus creating outcome measures totally off the chart or what was expected.

Now all we need to do is devise a table of different formulas that allow for statistical differences in measuring the hundreds (maybe thousands) of variables that occur in certain stressors are applied. That should be pretty simple. (Right!)
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Last edited by pegleg; 10-13-2013 at 02:55 PM. Reason: Sorry about the misspelling of "consensus" in the reply title!
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Old 10-13-2013, 08:42 PM #5
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Here is a very interesting report on AD but there is a lot of crossover- Pay particular attention to the links along the right hand edge of the screen-

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2905685/

Effects of Stress and Stress Hormones on Amyloid-β Protein and Plaque Deposition
Hongxin Dong* and John G. Csernansky
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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 10-14-2013, 12:22 AM #6
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Stress, i believe in my case, was a big factor in triggering my PD. But, there is another thing which I wonder if any one else experienced. I can only call it " selection of increasing the symptoms" under stress. I started a new position in the same company in September and nobody in my work knows that I have PD as far as I can tell. But, since staring my new position I experienced significant increased in slowness and rigidity on my left side but not increase in the tremor, which was my main symptom before when I was in a stressful situation. It's almost seem like I am experiencing more of the symptoms that I can hide and less that will be visible to others, but only for limited amount of time. Can a brain do that? I am not on any medication right now, but I was taking Mirapex for 8 months before stopping in June because of side effects. I am taking very small amounts of Mucuna but can't really say if it helps or not.
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Old 10-14-2013, 07:45 AM #7
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Quote:
Originally Posted by Bogusia View Post
Stress, i believe in my case, was a big factor in triggering my PD. But, there is another thing which I wonder if any one else experienced. I can only call it " selection of increasing the symptoms" under stress. I started a new position in the same company in September and nobody in my work knows that I have PD as far as I can tell. But, since staring my new position I experienced significant increased in slowness and rigidity on my left side but not increase in the tremor, which was my main symptom before when I was in a stressful situation. It's almost seem like I am experiencing more of the symptoms that I can hide and less that will be visible to others, but only for limited amount of time. Can a brain do that? I am not on any medication right now, but I was taking Mirapex for 8 months before stopping in June because of side effects. I am taking very small amounts of Mucuna but can't really say if it helps or not.
i have no tremor except when very tired, cold or stressed. not exactly addressing your question but my "progression" was never gradual, always seemed to be in discrete steps, i would wake up and just be "worse".
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Old 10-14-2013, 10:26 AM #8
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Default Does Stress or Anxiety Worsen PD Tremor or Dystonia?

Thoughts from Monique Giroux, MD:

http://drgiroux.com/october-2013-que...orsen-symtoms/
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Old 10-14-2013, 12:33 PM #9
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Being tired or cold are classic triggers for the stress response. And the "stairstep" changes are the "thresholds" moving and they do not return to their original location easily if at all.

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Originally Posted by soccertese View Post
i have no tremor except when very tired, cold or stressed. not exactly addressing your question but my "progression" was never gradual, always seemed to be in discrete steps, i would wake up and just be "worse".
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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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