Response to Sedona: I wish everyone with... - Cure Parkinson's

Cure Parkinson's

26,301 members27,661 posts

Response to Sedona

Kachimom profile image
1 Reply

I wish everyone with PD and their families could read your letter. I think you express what most all PD people struggle with. I was diagnosed only 5 years ago and I have finally come to the same conclusion. You try every day to maintain and figure out what I can do or take to keep it at bay and at the end of the day I have no answer. There are just too many inconsistentcies within you and the environment each day to ever get an solid answer. So the answer is? " no one knows". Put one foot in front of the other, keep moving, exercising, taking your meds and smile even if you don't feel like it.

Written by
Kachimom profile image
Kachimom
To view profiles and participate in discussions please or .
1 Reply
DeParkiePoet profile image
DeParkiePoet

Very well said!

Not what you're looking for?

You may also like...

Don't keep fixating on dopamine to alleviate your lack of energy.

Dopamine is just one(1) neurotransmitter within your system's complex of neurotransmitters....

To the newly diagnosed, one more time, straight talk

I will be blunt, sorry but there is not time nor ability to do otherwise. 1- What is PD My first...

An important message from former forum member "easilly"/Art to the forum members, SAFETY FIRST!!!

Dear Forum Members, Some of you may have noticed that I have removed all of Dr. Costantini's...

The Importance of 1) sleep, 2) exercise type, and 3) time of day: imperative to understand the correlation to minimize motor dysfunctions.

Preamble: I’m not a physician; I’m just a stupid PhD. biochemist (see my profile). I don’t answer...

Dr. Minchley – naturopath focused on PD – Sharon's take

Dr. Minchley – naturopath focused on PD – my take I have nothing against naturopaths. Bastyr...