Living with Parkinson's Disease - Meet others & come say hi
Welcome to the Parkinson's Disease group on Mayo Clinic Connect.
This is a welcoming, safe place where you can meet people living with Parkinson's or caring for someone with Parkinson's. Let's learn from each other and share stories about living well with Parkinson's, coping with the bumps and offering tips.
Chances are you'll to be greeted by fellow member and volunteer patient Mentor, Teresa (@hopeful33250), when you post to this group.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let's chat. Why not start by introducing yourself?
Interested in more discussions like this? Go to the Parkinson's Disease Support Group.
@pbarr Hello Tom and welcome to Mayo Connect. I am sorry to hear of all of the health problems your wife has had. The PD diagnosis must be a difficult one for her in addition to the other health issues.
What symptoms led to her PD diagnosis? Is she having problems walking or does she have tremors? Has she begun any PD medications?
My husband was diagnosed several years ago. Parkinsons of the Rockies has been very helpful to him with regular Parkinsons Boxing, stretching classes. There are people there in all stages of the disease and aside from the exercise they and their caregivers help and connect with each other. Nebraska also has an association, Parkinsonsnebraska.org. Check it out. I’m so sorry that your wife and you are going through this. Best of luck.
The meds she tried didn't help made her other conditions act up worse she thinks.
Trouble walking and use of her hands
@pbarrier1
I'm wondering if she has tried other meds to help with Parkinson's. Have you contacted her doctor to see if another medication might be tried?
If her worst symptoms are walking and use of her hands. She might be helped by working with a physical therapist (for the walking problem) and an occupational therapist who can help with the use of the hands.
Would she be willing to see a physical therapist?
After about 2 .months finally talked her in to ding therapy. Started about 2 was ago. She is talking about trying some patches costly but if it helps cost would not be a factor. Wondered if you have heard of anyone using a patch for pd?
Hello Rose
Hope you feel comfortable on this site.
Everyone I have been sharing with are very caring individuals. If you are not sure about something .. just ask.
Sillyblone
Hello Tom,
Welcome to the group.
Sillyblone
@pbarr
We have had several members talk about using the patch. Here is a link where you can see the discussions on this topic,
https://connect.mayoclinic.org/group/parkinsons-disease/?search=patch#discussion-listview
You mentioned in your post, "ding therapy." I'm not sure I understand what that is. Could you describe it for me?