Parkinson's Disease Tulip


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 10-06-2013, 09:12 PM #1
reverett123's Avatar
reverett123 reverett123 is offline
In Remembrance
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
reverett123 reverett123 is offline
In Remembrance
reverett123's Avatar
 
Join Date: Aug 2006
Posts: 3,772
15 yr Member
Default something new

This latest chapter began a couple of weeks back when I had become concerned with the erratic nature of my med response. One of the basic possibilities was that diabetes was creeping up on me. In the course of my research I came across info about the use of apple vinegar to drastically lower the glycemic index of ones' meal. This then led to the discovery of work that found that vinegars had properties that made them an ACE inhibitor completely independently of their glucose management abilities. ACE inhibitors are good for PWP because of their effect on mitochondria.

Still with me boys and girls? So here is the heart of the matter, at least for tonight. Starting about a week ago, I revisited some related work that Laura and I had explored about temporary paralysis that results from an interaction between insulin, potassium, and magnesium. I had shelved it back then due to concerns about potassium overdose. Overblown in most cases, my GP had OK'd up to 20 Molar units daily in my investigation of the possibilities in my own case. For a number of reasons I put it on hold.

Until last week, when I took another look at the file. I began taking magnesium citrate and potassium gluconate and guickly worked up to the previous targets.

Right away I could tell that something was going on. The fluctuations that had started me on this road were gone. I was taking less medication with levodopa/carbidopa down to about 600 mg today from about 2000 mg two weeks ago. And I am getting stronger, esp in my legs. Plus a decade long problem with constipation is much improved.

But all is not roses. There was a bit of dyskinesia at first, mostly in the evening. And, here is the big one, if I don't keepan eagle eye on the dosing I get mad as a hatter for about three hours or so around dinner time! I have had some illlicit affairs with various chemicals over the years so I know a little whereof I speak and I would describe it as being loopy as a git. I am aware of my actions and whereabouts and I pose no dangers to self or small mammals, but there is no denying that I am flat on my ***.

But why? Any ideas?
__________________
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.
reverett123 is offline   Reply With QuoteReply With Quote
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off



All times are GMT -5. The time now is 12:34 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.