FAQ/Help |
Calendar |
Search |
Today's Posts |
|
03-02-2007, 03:08 PM | #1 | |||
|
||||
Senior Member
|
The only rational basis that I can think of for my symptomatic relief so far is this..Robert and yourself have had pd for appox the same amount of time as myself..You began LDN about 2.5 years ago, as did Robert with the DM..(2 yrs ago)....If we were to play the devils advocate and assume that both of your progressions have been halted as the study suggests..or if it has slowed the progressions or masked your symptoms, or a combination of the above..and myself on the other hand..I definately have 2 years of uninterrupted progression..I have more symptoms to treat, keeping in mind that you both were in the early stages of pd when you began the LDN/DM regimen..Then again it could be that you are both in fact on the Sinamet honeymoon and I am merely enjoying the dopamine reuptake inhibitor consequences of DM..I think now that a few more folks in our community are interested in trying DM we will know one thing for sure..We still wont know for a number of years if it has halted our progressions but we will have some comparisons on symptoms
__________________
There are those who see things as they are and ask..Why?..I dream of things that never were and ask..Why not?..RFK |
|||
Reply With Quote |
03-02-2007, 06:34 PM | #2 | |||
|
||||
In Remembrance
|
First of all, there is more than one effect here. Symptomatic relief for Steve is a short term effect. Protection against further degeneration by quieting the immune system may be the case for Robert.
An additional possibility is endocrine effects on the HPA axis stress response resulting in Steve's sense calm at the podium. Taking a "Multihit" viewpoint, these may be three entirely separate effects acting via independent mechanisms. And one or more may be dose dependent and there is a 50% spread between Steve and Robert. With endocrine affairs a little goes a long way as well. Leaving Ashley out for now and just talking to the DM crew, have either of you tried either lower or larger doses? And have either of you tried taking it at a different time of day? -Rick Quote:
__________________
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. |
|||
Reply With Quote |
03-02-2007, 10:06 PM | #3 | |||
|
||||
In Remembrance
|
You seem to be doing well and are stable, so maybe you should be our "control" for now. Another week to let the MAO wash out and I will start low but then inch up a little above you to see what happens. So long as there are so few of us we can take it slow and easy. I did buy some of the local pharmacy's finest today. Did you know they had it in the five gallon size?
__________________
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. |
|||
Reply With Quote |
03-03-2007, 12:13 AM | #4 | |||
|
||||
Senior Member
|
Bucket o' DM..Wonder what the street value is?.. ..At 1/2 teaspoon per night that should last me for the rest of my life..
It will be interesting to compare results
__________________
There are those who see things as they are and ask..Why?..I dream of things that never were and ask..Why not?..RFK |
|||
Reply With Quote |
03-03-2007, 03:37 AM | #5 | |||
|
||||
Wisest Elder Ever
|
There are other forms of DM you can use.
Delsym is pure DM in sustained release dosage form. Most pharmacies carry it: http://www.delsym.com/ Some people get nausea from the guaifenesin in Robitussin DM. So if you prefer single dose DM the Delsym is for you. But it costs more. There are tablets also, with guaifenesin and DM 30mg sustained acting: Mucinex DM http://www.mucinex.com/pdf/Mucinex_DM.pdf Some stores now have a generic available for this. Kids abuse DM so if you begin to use it in high amounts, you may attract attention in the store. Some pharmacies may have it behind the counter because of this. Coricidin HBR recently was targeted by abusers and is often behind the counter now. Very high dosing of DM can cause dissociative CNS symptoms and a peculiar "buzz"...but in the doses mentioned here, that should not be a problem. Here is more information: http://www.nhtsa.dot.gov/PEOPLE/inju...methorphan.htm Quote:
This is also interesting: Quote:
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are 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.
|
|||
Reply With Quote |
03-03-2007, 11:15 AM | #6 | |||
|
||||
Member
|
MRSD, Delsym and some other long acting DM (aka DXM) preparations also contain polystiril, a substance that slows down the absorption of the drug. I was told by someone who is actively doing research on this class of drugs that using the long acting forms will defeat production of the "spike" of concentration of DM produced by the mini-dose that is needed.
Also, the time it is taken, just before bedtime, is important for producing a brief blocking of the opioid receptors just before the natural period of release of endorphins (2 to 4 am) the hormones that are beneficial in calming the over-active microglial cells in the PD midbrain. Too much drug, or taken at the wrong time, may cause prolongned receptor inhibition, or inhibition at a sub-optimal time for taking advantage of boosting the normal endorphin release. This is my opinion, based on what I have learned from other scientists who have studied the process extensively in the laboratory for the last ten or twelve years. Robert |
|||
Reply With Quote |
Reply |
|
|
Similar Threads | ||||
Thread | Forum | |||
My Order of Protection returned to court - DAMN | Bipolar Disorder |