Sorry, that question could not be found.  

Connect with others who understand.

Sign up Log in
Resources
About MyParkinsonsTeam
Powered By

Top 10 search results for "how do you deal with family members that just dont understand why youre not who you used to be and cant do the things you used to do" in Q&A. To see all results and access other features, sign up for free.

I Have Developed Droop Neck I Do Neck Exercise But Little Improvement I Have Very Short Walking Distance. I Am 77 And Have 13 Years Diagnos

A MyParkinsonsTeam Member asked a question 💭
Newport News, VA

Has anyone found neck or back supports helpful

•
View reactions
A MyParkinsonsTeam Member

After seeing this picture, I'm thinking of buying a neck pillow (type you use on an airplane) for my hubby.

Family Needs To Understand MY Disorder

A MyParkinsonsTeam Member asked a question 💭
Houston, TX

Because I fall a lot, cannot stand for long periods of time, shakes a lot, trouble walking, etc. I just want them to know I am not seeking or want sympathy or feeling sorry for myself. I cannot cook a lot like I used too. I almost fell into the oven, so I only cook when someone is home. I am alone from 7am-7pm. I have no friends that visit, or call. I just want ppl to understand I cannot walk, run, and clean like I used to do. I try but I also have congestive heart failure. I just want… read more

•
View reactions
A MyParkinsonsTeam Member

Parkinson’s is not easy for people who can’t feel what it’s like. Some people with Parkinson’s freeze. From their perspective, they’re wondering why you don’t just take a step. They tend to get… read more

Any Suggestions On Best Way To Improver Handwriting? I Understand Its Typical....I Start Large And Gets So Tiny Even I Can't Read It.

A MyParkinsonsTeam Member asked a question 💭
Houston, TX
•
View reactions
A MyParkinsonsTeam Member

Try coloring books , every day,children's or adults,crayons or pencils,I found it helps a lot!!!!!

Do You Think Your Family And Friends And Even Your Neurologist Understand Parkinson's Disease And How It Affects You As A Person?

A MyParkinsonsTeam Member asked a question 💭
Bell Buckle, TN

This disease is the worst to comprehend as a patient and as a caregiver. I stay isolated and alone because people are afraid of me. When I tremor and my arms are flailing out of control, they think I am being aggressive. When my facial expression is frozen and I can't turn my head and have trouble with speech, people think I am ignoring them. People are constantly telling me not to be nervous to just relax. Really, I could scream every time I am told this. There is no way to communicate my… read more

•
View reactions
A MyParkinsonsTeam Member

K4SGA, Amen! He is my anchor!

Why Do So Many Members Mention Their Occupation & Qualifications In Their Stories? I Am Not Interested In What You Did But Who You ARE Now!!

A MyParkinsonsTeam Member asked a question 💭
Meyerton, ZA
•
View reactions
A MyParkinsonsTeam Member

Lani, I hope these instructions help you.

What Is The Worst Thing That People Can Say To Someone With Parkinson's? What Are Some Of The Irritating Things That People Have Said To You

A MyParkinsonsTeam Member asked a question 💭
Mesa, AZ

I am so tired of people who say take this take that or that their brother had The shakes, this helped him
I'm sick to death of it. I'm tired of people saying well it can't be that bad I'm tired of people saying well you don't need to keep going to all these different doctors. I'm fed up with people trying to give me medical advice. I have surrounded myself with people that I trust my MDS my physical therapist and my psychiatrist. If I trust someone that can help me I will do whatever they say… read more

•
View reactions
A MyParkinsonsTeam Member

You don’t sound disabled
over the phone ? What does a disability sound like and that’s when I called the Social Security office

Advanced Warning; I Won't Be Posting Anymore After I'm Dead.

A MyParkinsonsTeam Member asked a question 💭
Woking on Sea UK

When I die I won't be posting any longer but my wife will post a brief message saying something like he's gone ! However .........

If you make weekly visits to an elderly friend living alone with failing health you're likely to notice when they die but what about on line ? You may have conversed for years knowing only their name on a forum. No address to write, No email, No phone, some knowledge of family and friends but no way of contacting any of them and one day they're gone. Silence. No… read more

•
View reactions
A MyParkinsonsTeam Member

I have provided my daughter with all my contacts that she she would contact

How Do You Explain Parkinson’s To Your Friends And Family?

A MyParkinsonsTeam Member asked a question 💭
San Francisco, CA

How do you explain Parkinson's to your friends and family? Do you think they understand?

•
View reactions
A MyParkinsonsTeam Member

I hid when I was diagnosed with Epilepsy. I told my husband I will not do that again. I told all my friends and family.

Are You Honest?

A MyParkinsonsTeam Member asked a question 💭
Mesa, AZ

Are you honest with your family and friends about how you really feel? Are you honest about your physical or your emotional difficulties?

Yes, or no? And why

🦉

•
View reactions
A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member How honest is a chity chity bang bang? It's not, but it rolls off the tongue better than 'excrement excrement flatulence flatulence '
🤔😟🙂😀😄

I Often Distrust People I Love, And Find I Don't Believe What They Tell Me. Does That Qualify As A Delusion?

A MyParkinsonsTeam Member asked a question 💭
Mount Pleasant, MI
•
View reactions
A MyParkinsonsTeam Member

My late husband had Alzheimer’s. When he went on his flights I asked questions about what he was doing, and I tried to use the questions as a way to bring him back to reality.