COMMUNITY
Community is one of the three primary pillars for the NeuroSpark Foundation, and we take the information we provide for you seriously, well-thoughout, and completly sourced for accuracy.
As we wanted to get the website out as soon as possible, we were not yet satisfied with our current Community information, and didn't want to just put out information . . . to put it out.
We will be adding more information daily, so please come back to visit and discover more about how to be your own best advocate!
JOIN US IN OUR FREE ONLINE ZOOM GROUP!
These meetings are where we learn from experts and each other on how to live life with DBS for any condition it is used as a therapy!
If you would, please fill out the form below. It helps us protect the group and provide a safe place to talk freely and openly!
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NOTE: None of your data is sold or shared and by completing this form you will get emails for our meetings and announcements.
DON'T TAKE OUR WORD FOR IT . . .
The NeuroSpark Foundation is not a group of doctors or a hospital, but a community of people living with deep brain stimulation, care partners, and allies who have learned to ask hard questions and dig into the research.
We read medical papers, follow experts, and share trusted sources so you can check information yourself and bring stronger questions to your own medical team. Nothing here is medical advice, and only your doctors can tell you what to do, change, start, or stop; our role is to help you understand the language, find solid information, and become a more confident self-advocate in your care.