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- [Understanding Parkinson's](/understanding-parkinsons)
- [Getting Diagnosed](/understanding-parkinsons/getting-diagnosed)
 
  ## Breadcrumb

- [Home](/)
- [Understanding Parkinson's](/understanding-parkinsons)
- [Getting Diagnosed](/understanding-parkinsons/getting-diagnosed)
 
 #  Coping with a Diagnosis 

 

   

  ## 💡 Quick Summary 

 - Emotional adjustment to Parkinson’s involves a range of feelings including denial, shock, discouragement, frustration and identity changes.

- Each person experiences these stages differently and may revisit them as new challenges arise.

- Practical impacts include changes in abilities and family roles, requiring more time for tasks and causing stress, which may worsen symptoms.

- Recognizing these changes helps manage daily life and maintain independence.

- Support, utilizing resources and connecting with others with PD can provide encouragement and guidance for navigating life with Parkinson’s.

 

   ![coping with a diagnosis](/sites/default/files/styles/no_sizing/public/images/copingwithadiagnosis.jpg?itok=EhBVkBNI)  When you or a family member is diagnosed with Parkinson's disease (PD), you will experience a range of emotions and go through several stages of adjustment to the disease. As PD progresses and brings new challenges, you will go through many of the emotions and stages of adjustment anew. Each person experiences stages in their own order and at their own pace.

  ##  Denial, Disbelief, Shock 

 Denial can be a useful coping mechanism if it allows you to largely ignore symptoms and go on with life as usual. However, if denial leads to the refusal to take medication or going to extremes seeking multiple second opinions, it may indicate denial as an unhealthy response.  
   
 This response may be prolonged if symptoms are mild or the correct diagnosis is not made early after symptoms arise.

 - ###   What You Can Do   
    
    
    - Take time to explore your feelings and be honest with yourself and others. Journaling or [telling your story](/living-with-parkinsons/my-pd-story/submit "Submit Your Story") may help.
    - Knowledge is power. Learn about Parkinson's and focus on abilities rather than inabilities.
    - Remember, each person's Parkinson’s experience is unique.
 
  ##  Discouragement, Searching for an Explanation 

 In this phase, people look for some direct cause for the health problems they are experiencing. You might become preoccupied with asking yourself "why me?" while searching for something or somebody to blame for the unwanted circumstances occurring in your life.

 - ###   What You Can Do   
    
    
    - Symptoms of depression are common in any stage of PD. In some cases, depression is an early symptom. Tell your doctor if you feel depressed.
 
  ##  Shifting Abilities, Role Reversals 

 People with PD often need more time to perform activities because of changes in hand coordination, muscle stiffness or slowness. Conflict may arise as it becomes necessary to reevaluate who is responsible for what tasks in the family and around the home.  
   
 Changing abilities and assuming new roles can cause frustration and emotional upheaval, while stress makes PD symptoms worse.

 - ###   What You Can Do   
    
    
    - Maintain open communication with your loved ones.
    - Prioritize daily tasks. Get outside help as needed for some tasks such as yard work, housecleaning or home maintenance.
    - Regular exercise can help manage stress.
    - Seek help from a counselor to resolve relationship conflicts.
 
  ##  Identity Change 

 At this stage, you may realize that PD has impacted your life. You are willing to take on the work to achieve your optimal level of independence and connect with others who share the same condition for education and encouragement.

 - ###   What You Can Do   
    
    
    - Explore new opportunities to find self-fulfillment.
    - Find new ways to adapt to the new circumstances.
    - You once again feel some control in your life.
    - Take an active role in your health and care. Work with your health care providers to optimize your medications.
    - Communicate openly about your priorities.
    - Set realistic expectations.
 
 Remember that you are not alone. One million people in the U.S. and 10 million people worldwide live with PD. These estimates do not account for cases of PD that are unreported, undiagnosed, or misdiagnosed. With a diagnosis and the freedom to learn at your own pace, you can begin to understand PD, its treatments, and the role they will play in your life. Your diagnosis can be the first step to taking charge of your life with PD. What are some next steps?

 ###  How to Talk About Your Parkinson’s Diagnosis 

Sharing a Parkinson's diagnosis with family, friends or coworkers can feel overwhelming. Taking time to think through what to say can help you feel more prepared.

 [Learn tips for starting the conversation](/living-with-parkinsons/new-to-parkinsons/talk-about-your-diagnosis) 

 

 ### Hear Stories from People with PD

It is common for many people to experience a wide range of emotions upon diagnosis from shock, to anger and even to sometimes a sense relief at being able to name symptoms (perhaps a small tremor or weaknesses) that have gone unexplained or misdiagnosed for years. Hear from others who may have had a similar experience similar. Start with [My PD Story](/living-with-parkinsons/stories "My PD Story").

  ##  Find Resources That Help 

  ###  Helpline 

Call or email our Helpline at 1-800-4PD-INFO (1-800-473-4636) for answers to your questions — from PD information to referrals to nearby specialists.

 

 [FIND ANSWERS](/resources-support/helpline) 

 ###  New to Parkinson’s? 

We offer the community, resources and advice to support you and your family as you begin to build a better life with Parkinson's.

 

 [LEARN MORE](/living-with-parkinsons/new-to-parkinsons) 

 ###  Local Classes and Expert Care 

Use our search tool to find medical centers that specialize in Parkinson’s, nearby specialists, your closest Chapter and local resources.

 

 [FIND LOCAL RESOURCES](/your-area) 

 

 *Page reviewed by Dr. Lauren Fanty, Movement Disorders Fellow at the University of Florida, a Parkinson’s Foundation Center of Excellence.*

  ##  Related Materials 

   Books 

###  [ Newly Diagnosed Guide ](/library/book/newly-diagnosed-guide) 



 [Read Now](/library/book/newly-diagnosed-guide)

   Videos &amp; Webinars 

###  [ Expert Briefing: Mental Health and PD ](/library/videos/mental-health) 



 [Watch Now](/library/videos/mental-health)

   Podcasts 

###  [ Episode 91: The Newly Diagnosed Experience ](/library/podcast/91) 



 [Listen Now](/library/podcast/91)

  

  ##  Related Blog Posts 

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 Tips for Daily Living 

###  [ Parkinson’s Q&amp;A: How do I find information after a new diagnosis? ](/blog/tips/information-after-diagnosis) 

 

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###  [ Parkinson’s Q&amp;A: How long does it take to accept a Parkinson’s diagnosis? ](/blog/awareness/accepting-diagnosis) 

 

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 Tips for Daily Living 

###  [ Newly Diagnosed: Living Your Best Life with Parkinson’s ](/blog/research/newly-diagnosed) 

 

  READ NOW  

 

  

 ###  Connect with Others 

 Explore our PD Conversations discussion groups to find answers or talk to others going through similar experiences.

 [Join Now](https://www.pdconversations.org/) 

 

 

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