Where Do I Begin To Understand This Disease? It Is My Father, Not Me Yet, Who Has Been Diagnosed.
Read all you can about the disease and treatments
Hi - I suggest that you contact the National Parkinsons Foundation (www.parkinson.org). They have a lot of information and are very helpful. Also, the Michael J. Fox organization has been having 1 hour seminars online monthly which gives information for Parkinson's patients that is very helpful. If you contact them, they may have information that can also help you.
I do not think my dad would want me talking to his Dr. Scott and White here has a special section for Parkinson's. I will look for that book. So far what I read is very confusing.
We are lucky to have a support group offered by a hospital in our area. Check your area for one or ask your dads doctor if he knows of one. It helps to talk to other caregivers.
How Many Out There Have Parkinsonism? Do You Know The Difference Between Parkinsonism And Parkinson's?
Has Anyone Been In Touch With A Dr. Craig Koehler? I'm Afraid Of The Prescription Side Affects And Their Eventual No Longer Working.
I Often Distrust People I Love, And Find I Don't Believe What They Tell Me. Does That Qualify As A Delusion?