Quick Question: March 2025 Please enable JavaScript in your browser to complete this form.Please enable JavaScript in your browser to complete this form.What types of FTD-related research content would you find most valuable? *Clinical trial updatesData privacyDisease progression and symptomsEfforts to improve quality of lifeGene therapyGenetic FTD researchHow the Registry uses your dataHow to prepare for and participate in clinical trialsPersonal stories from research participantsQuestions to ask when thinking about research participationResearch advocacy and awarenessResearch into causes and risk factors for FTD disordersSteps in drug developmentSpeech and communication therapiesUpdates on FTD disorder diagnostics and biomarkersWhat is informed consent?Other:Other researchPlease Identify yourself: A person diagnosed with FTD, answering for myselfA biological family member, answering on behalf of an FTD-diagnosed personA spouse, answering on behalf of an FTD-diagnosed personA caregiver, answering on behalf of an FTD-diagnosed personA friend, answering on behalf of an FTD-diagnosed personA biological family member, answering for myselfA spouse, answering for myselfA caregiver, answering for myselfA friend, answering for myselfOther...Identify yourself - Please specifyWhat part of the FTD journey are you and your loved one currently on?Select OneNewly diagnosed or mild cognitive declineMid-stage or moderate cognitive declineLate stage or severe cognitive declineMy FTD diagnosed loved one has passed onYour Gender:Select OneFemaleMaleNon-BinaryPrefer not to answerSubmit
