• Facebook
  • Instagram
  • Twitter

Get Support – Call 1-888-MITO-411

  • Shop
  • Events
  • Donate
MitoAction

MitoAction

Support, Education, Outreach and Advocacy for Children and Adults Living with Mitochondrial Disease

  • Mitochondrial Disease
    • About Mito
      • New Patient Kit
      • Types of Mitochondrial Diseases
      • Symptoms
      • Treatment
      • Mito FAQ’s
      • Mitochondrial Disease News
    • Diagnosis & Care
      • Diagnosing Mitochondrial Disease
      • Find a Mito Doctor
      • What is a Mito Cocktail?
      • Mito Sick Protocol
      • Clinical Trials & Studies
    • Day to Day with Mito
      • Living with Mitochondrial Disease
      • Care Management
      • Managing Your Energy
      • Traveling with Mito
      • Navigating COVID-19
    • For Medical Professionals
      • Mitochondrial Care Network
      • Monthly Expert Series
  • Fatty Acid Oxidation Disorders
    • About FAODs
      • Types of FAOD
      • Symptoms
      • Diagnosis
      • Treatment
    • FAOD Programs and Support
      • New Patient Kit
      • FAOD Support Calls
      • FAOD Experts Series
      • FAOD Resources
      • International Metabolic Conference
  • Programs & Support
    • Support
      • Mito411
      • MitoAction Memories
      • MitoPlaydates
      • MitoSocials
      • MitoChampions
      • Support Calls
      • Positive Peach Packages
    • Programs
      • Dalia’s Wish
      • Matthew Harty Camper Fund
      • Marcel’s Way Family Fund
      • MitoSantas
      • MyMito App
    • Education
      • Monthly Expert Series
      • Wondering Wednesdays
      • Energy In Action Podcast
      • Energy 4 Education
      • Patient Education Forums
      • International Metabolic Conference
    • Resources & Planning
      • Health Insurance
      • Disability Benefits
      • Mobility Devices
      • Vehicle Modification
      • Estate Planning
      • Medical Child Abuse
  • Join the Cause
    • Giving
      • Donate
      • Honor and Memorial Giving
      • Another Helping
      • Matching Gifts
      • Shop for MitoAction
      • Giving Tuesday – Ways to Give
    • Events
      • International Metabolic Conference
      • MitoAction Energy Walks
      • Sandra K. Russell Derby Day Benefit for Mito
      • Matthew Harty Camper Fund Events
    • Volunteer
      • Host a MitoSocial
      • Host a MitoPlaydate
      • Create a Fundraiser
      • MitoChampions
      • Share Your Ideas
    • Raise Your Voice
      • Take Legislative Action
      • Mitochondrial Disease Awareness Week
      • Light a Light
  • About Us
    • Contact Us
    • Connect on Social
    • Our Team
    • Meet Our Partners
    • Newsletter Signup
  • Show Search

Top 10 Tips for Empowerment & Being Your Own Advocate

Print Friendly, PDF & Email

ENERGY IN ACTION – EPISODE 051
Top 10 Tips for Empowerment & Being Your Own Advocate

Cristy Balcells is the Associate Director of Patient Advocacy and Public Policy for Zogenix and the mother of Eva, who has Leigh Syndrome, a type of mitochondrial disease. Christy joins me for a conversation around empowerment and shares her list of 10 tips for being a great mitochondrial disease advocate for yourself or someone you care for. 

EPISODE HIGHLIGHTS

Become an expert in your own disease

Get an accurate diagnosis because without a specific diagnosis, a lot of doors are closed to clinical trials, insurance coverage, participating in a patient registry or general eligibility for treatment. After you have a diagnosis, become an expert on your disease and diagnosis because no one will be invested in it like you are, whether for your child or yourself.  

Know your baseline

Baseline is a medical concept important for clinical trials. Determine your baseline by considering your average good days and bad days. Know and document your baseline so if you start a new treatment or therapy, you can identify how it’s affecting your disease.

Tell people about your disease and know how to ask for support

To set boundaries, use a script and be specific that you’re not seeking advice, only support. Practice saying, “I’m going to talk to you about something I’m dealing with and I don’t need your advice. I just want you to hear me and be there for support”. If someone asks how they can help, provide options that would be helpful.

Reflect like an interviewer

Allow questions to serve as an opportunity to raise awareness about your disease and always restate a question in your answer. 

Keep good records

Use technology to stay organized and ensure your medical records are accessible. Keeping thorough and well-organized records is easier for you, but also helps when you have an opportunity to participate in a clinical trial, research study or equipment grant.

Stay informed

Subscribe to all of the newsletters on patient sites because knowledge is power. Set up Google alerts for keywords which will provide you a periodic digest around the keyword. You can also stay informed by joining social media or local support groups.

Prioritize your symptoms and set goals

You won’t be able to address every concern in every appointment, so prioritize your symptoms to discuss them with your physician. Daily tracking of your baseline data will help you know if symptoms are improving or getting worse and know if the symptom should be prioritized at your next check-up. 

Be a micro influencer

Documenting your journey can spread awareness to other people. Micro influencers in the disease space are respected and powerful because they make a difference.

Hire yourself

You are the Director of Communications for yourself or your child’s diagnosis. Provide updates and check in regularly with everyone on your team and keep developing relationships in your network. 

Amplify your voice

Your experience is valuable and only you can share it. No one else can represent your experience. Participate in clinical trials, patient registries, surveys and interviews. 

RESOURCES & LINKS MENTIONED

Zogenix — https://zogenix.com/

MayBeMito — https://www.maybemito.com/

MyMito App — https://www.mitoaction.org/mobile_new/

AllStripes — https://www.allstripes.com/

UMDF — https://www.umdf.org/

Cure Mito — https://www.curemito.org/

International Mito Patients — https://www.mitopatients.org/

Mito Canada — https://mitocanada.org/

Create a Google Alert — https://support.google.com/websearch/answer/4815696?hl=en

Life with a Vent — https://www.youtube.com/channel/UCHwOT3pjEA3EgShKomTuTDw

The Mito Girl — https://www.instagram.com/themitogirl

Jeremiah Gracen TK2D Warrior — https://ne-np.facebook.com/JeremiahGracenTK2DWarrior

Upcoming
Events

View All
Sep 27
8:00 pm - 9:00 pm Event Series

Wondering Wednesdays: Ask the Genetic Counselor

Sep 28
1:00 pm - 2:30 pm

FAOD Monthly Afternoon Support Call

Sep 29
12:00 pm - 1:00 pm Event Series

Weekly Support Call

View Calendar

Expert
Series

View All

Upcoming Presentations

Nov 1
7:00 pm - 8:00 pm

Expert Series: LCHADD Retinopathy Update: Moving Toward a Treatment

Nov 3
12:00 pm - 1:00 pm

Expert Series: Immune Cell Function in Mitochondrial Disease

View Calendar

Last Presentation

Expert Series: At the crossroad of mitochondrial disease and mitochondrial dysfunction
Presented July 25, 2023

P.O. Box 310
Novi, MI 48376
(888) 648-6228
info@mitoaction.org

  • Support
  • Resources
  • Donate
  • Events
  • Subscribe
©2023 MitoAction. All Rights Reserved. Website by ThinkGenetic, Inc.

Privacy Policy. Terms of Use.