Print

Print


It must be really frustrating to be given the runaround for so long. From
reading other contributions to the list, you aren't alone. It seems to me
that some physicians are more concerned with fitting us into neat diagnostic
boxes rather than accepting that nature can be pretty untidy. Just because
you don't have all the classic symptoms of PD, you can't have PD,same for
AD. But why shouldn't you have some of this and a little of that? Nature
doesn't know that you need to be labelled, lined up, photographed and boxed!

As to your questions, pass on 1, don't know how effective the drugs will be
at such levels.
2. From what I read and hear, dyskinesia (she's a beaut word alright)is the
result of too much dopamine compared to your deficiency. If you have a
chronic deficiency you should be able to soak up more dopamine before
feeling unwanted side effects. If it does get unmanageable, you'll probably
be put on a combination of levadopa with an agonist.
3. If these large doses cause nausea, taking them with food can help (that's
the plus) but boosting the level of protein in your blood will reduce the
effective transport of levadopa out of your gut, through the bloodstream and
into the brain. So, if you have to eat, then low protein high carbohydrate
meals are recommended for the active parts of your day. But you still need
protein, (though probably less than you imagine), so save the proteins until
late in the day when it won't matter if the medication is less effective.
Ideally, you should accustomise yourself to taking the meds without food,
then slow uptake isn't a problem.
Hope this doesn't disagree widely with the many other opinions you are bound
to get on this.
Alf,
Adelaide, Aust
50/<1/48