@cindylb

It sounds as if you have covered a lot of areas of concern, given his symptoms.

Will you keep us posted as to how your husband is doing?

Teresa

I will keep you posted. I read the material on the site you provided the link for and it was very insightful and helpful. I'm always looking for information to try and resolve this unknown malady (so far) that my husband is suffering.

@cindylb

Getting a diagnosis is the tough part of PD. It took me about 15 years. I hope your husband's journey is a little shorter than mine.

Here is another website that you might find interesting, or at least helpful - http://www.parkinson.org/. You can get a lot of info about the different forms of PD, including many non-motor symptoms.

We will look forward to hearing from you again!

Teresa

Dear Teresa,

Thanks so much for the website...just opened your message.  Just getting to know how Connect works. The PD community is very helpful to dystonia because so many of PD also have dystonia.

Our research foundation to the DMRF, Dystonia Medical Research Foundation where I specifically go for my problem.  However, since dystonia is a neurological movement disorder

I go to many PD meetings and learn so much and get so much hope.

Many with PD are getting better and better with all of the new research if the patient is able to do

the exercises and treatments.

Appreciate your note and apologize for not responding sooner.

Kristina in D.C.