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Post COVID-19 Vaccine Registry for Patients with Mitochondrial Disease
Dear Patients and Families,
This is an anonymous survey which takes about 10 minutes to complete. The objective of this survey is to understand the potential side effects of the COVID19 vaccine for patients with mitochondrial disease.
Responding to this survey at any time is entirely voluntary.
You are eligible to participate in this survey if you are at least 18 years of age and are a patient with mitochondrial disease or caregiver of an individual with mitochondrial disease.
This survey includes questions about your experience as a patient or caregiver affected by mitochondrial disease during the COVID19 pandemic. Furthermore, the survey will ask you about the type of mitochondrial disease the individual has and experiences related to the COVID19 vaccine.
Aggregate survey data will be shared within the NIH and published. No individual data will be shared. Only the study team will have access to individual answers, without any identifiers. NIH (National Institutes of Health), UMDF (United Mitochondrial Disease Foundation), NAMDC (North American Mitochondrial Disease Consortium), PALS (People Against Leigh Disease) and RDCRN (Rare Disease Clinical Research Network) officials will not know whether or not you respond to the survey.
Responses to the survey (or lack thereof) will have no bearing on your relationship with the NIH, UMDF, NAMDC, PALS, or RDCRN.
There are no right or wrong answers to these survey questions. All responses can be edited at any time prior to final submission. If an area is "grayed out" simply click on it again and it will become active.
If you should have questions or concerns about the study or survey, please contact our study team.