Epilepsy Talk

Adult Epilepsy Support Groups | November 2, 2013

One thing I’ve discovered is the search for support groups is endless — and seldom successful. Unless you live in a metropolitan area.

But, if you do find a support group, you’ll find an amazing wealth of camaraderie, compassion and caring.

Not every group does the same things. Even groups with similar activities may have different results because of the individuals involved…but think of it as a learning and bonding experience.

You’re interacting with people who share a similar illness, but perhaps different solutions. You can share your feelings, fears, concerns and perhaps get answers.

But most importantly, you can join a community of caring and know that you’re not alone.

To be honest, I’ve started a support group with the help of my local EFA and a local hospital – complete with an epileptologist!

We have an established time and place to meet…with some materials available…snacks…and occasionally a guest speaker. Plus, everybody gets their fair share of time in with questions, suggestions and even resources not everyone’s familiar with.

I know that starting a support group is definitely not for everyone. However, there are resources available where you can get the help – and materials – you need.

The Epilepsy Foundation, as I found out, is only too eager to help…affiliates can provide information and referral assistance; maintain individual and family support services. To find one in your area simply enter your zip code, state and hit “search.” http://epilepsyfoundation.org/aboutus/AffiliateLookup.cfm

There’s another interesting group I found called “Epilepsy Meet-Up” where you can meet other local people with epilepsy. Friends and family members are also welcome. On the site, there’s an interactive map of Epilepsy Meet-Ups around the world. (And if you want to start or find a support group, this could be a good place to know about!) http://epilepsy.meetup.com/

“Add Coach” provides advice on how to start and run a support group. http://www.addcoach4u.com/support/howtostartasupportgro.html

Now, here’s a list of Adult Epilepsy Support Groups across the country that I’ve compiled. Each is listed by state, alphabetically. Hopefully it will be of help.

And don’t forget to look up Teen Epilepsy Support Groups. https://epilepsytalk.com/2012/05/07/teen-epilepsy-support-groups/

If you have any additions or suggestions, please, sing out!!!


The Central Alabama Epilepsy Support Group is committed to improving the lives of the people who experience epilepsy through education, awareness and peer support. http://www.meetup.com/Central-Alabama-Epilepsy-Support-Group/


The Epilepsy Foundation of Arizona has support groups in Phoenix (Spanish Speaking), Yuma, Sierra Vista, and Phoenix. http://www.epilepsyaz.org/programs_support

Arizona — Mesa — East Valley Epilepsy Group


The END Epilepsy Groups of Greater Los Angeles is composed of an Adult Therapy Group, Family & Friends and Women with Epilepsy as well as a Sibling Network. Each group and even each gathering may have a different topic or focus but, over a period of time, participants will benefit from the mutual therapy, education, socializing, self-help and idea-sharing. http://epilepsyfoundationgla.org/api/Index.cfm/cms.page/i/4145/Support-Networks/.

The Epilepsy Support Network of Orange County, CA has an Adult Educational Support Group, Teen Club, Emotional Support Group for Parents, On-Line Support Group for Parents, Mom’s Night Out, Special Needs Child Care and Community Presentations. http://www.epilepsysupportnet.org/html/services.html

The Epilepsy Foundation of San Diego County, provides Individual and Family Counseling, plus Crisis Intervention to help in the process of learning to cope successfully with epilepsy, as well as with the life issues impacted by epilepsy. http://www.epilepsysandiego.org/index.asp?f=supserv


The Connecticut Epilepsy Advocate has five support groups which meet monthly. They include: Adults Living With Epilepsy, Ability Beyond Disability, Middletown Parent Support Group, Stamford Support Group and Groton Support Group. http://www.ct-ea.org/supportgroups.html


Florida State Support Groups link you to meetings in communities throughout the state. To locate a support group near you, locate the county you live in or the closet county. The groups are generally free and open to anyone with epilepsy. Some groups are also open to friends and family members.http://www.doh.state.fl.us/family/epilepsy/Support.html


The Epilepsy Foundation of Hawaii provides information and educational services to individuals and groups with questions pertaining to epilepsy. The EFH’s mission is to increase public awareness of epilepsy and to build a sense of community, enabling those with epilepsy to participate fully in the community at large. http://www.hawaiiepilepsy.com/


The Epilepsy Foundation of Greater Chicago. Whether you’re a parent of a child with newly diagnosed epilepsy and in search of guidance from those who’ve been there, an adult with epilepsy who’s looking for advice and encouragement from others, or just someone looking for camaraderie from others who understand the challenges of living with epilepsy, they have a support group that will probably help you. They also have groups specially designed for caregivers and loved ones. http://www.epilepsychicago.org/programs-services/support-groups/

The Epilepsy Foundation of Greater Cincinnati includes support groups in Milford, Mason, Wilmington and Hamilton. The support groups are adults with epilepsy, parents, families and caregivers of those affected with epilepsy. The purpose of the groups is to come together to share tips, mutual concerns, common issues, challenges and successes with other members of the group. http://www.cincinnatiepilepsy.org/programs/support-groups/

The Epilepsy Support Program for McHenry County in Crystal Lake is for children and adults with epilepsy. Their program is to support you and your family with: Individual information and education, referrals, community and school education of epilepsy, monthly support group meetings, development of an individual seizure plan and seizure clinics. http://www.optionsandadvocacy.org/index.php/programs/epilepsy-support-program


Mercy Medical Center and the Greater Des Moines Area Epilepsy Foundation have partnered to provide two support groups for epilepsy patients and their families. http://www.mercydesmoines.org/events/EpilepsySupportGroups.cfm


The Epilepsy Foundation of Kentuckiana offers additional support groups and educational opportunities for the public throughout the year in various Kentuckiana locations. Right now, there are support groups in Lexington and Murray. http://www.epilepsyfoundation.org/local/kentuckiana/groups.cfm

The Northern Kentucky Epilepsy Support Group meets in Florence. http://www.cincinnatiepilepsy.org/programs/support-groups/


The Epilepsy Foundation of the Chesapeake Region is part of The Abilities Network Epilepsy Services Program which serves individuals, families, and the greater community with epilepsy education, information and referral services, assistance with medical issues, advocacy, support groups and scholarship support. Included are Anne Arundel County, Baltimore County, the Tri County Area (Calvert, Charles & St. Mary’s Counties), Frederick County, Harford County, Howard County, Montgomery & Prince George’s Counties, plus Western Maryland. http://www.virginianavigator.org/vn/support-group-epilepsy/epilepsy-foundation-chesapeake-region/program-79098.aspx


Epilepsy Support Group has meetings held at UMass. Memorial Health Center, 55 Lake Avenue North. Call for details. CONTACT: Marsha Williams, 508-856-4147

Southwest of Boston Parent &Family Support Network Group: Meets 1st Tuesday monthly (not July through Sept. and Dec.) from 7:30-9PM at the Medfield Town Library, 468 Main Street (Rte. 109). For parents of children and teens with epilepsy. CONTACT: Michelle Gaudet or Christi Barney, c/o EFMRI, 617-506-6041, Ext.19


The Epilepsy Support Group of Michigan has monthly “Learn & Share Conference Calls,” covering different topics such as Managing Memory Problems, Women and Epilepsy, Epilepsy Surgery, Ask the Epileptologist, Ask the Pediatric Epileptologist, Stress Management, Advocating for Students with Epilepsy, Diagnostic Tools for Epilepsy: From EEG to PET Details, Employment Issues for People with Epilepsy and Open Discussions. http://www.epilepsymichigan.org/page.php?id=278

Kalamazoo, hosted by Bronson Hospital. The group meets every other month on the LAST Wednesday of that month, from 6:30 – 7:30 pm in the Medical Office Pavilion M124. In our NeuroscienceCenter, we meet in the lobby. The group is for PWE and caregivers of PWE. For more information call 269-341-8383 and ask for Marcell.


The Minnesota Epilepsy Foundation. St. Paul is the central location for the support groups in Minnesota and meets once a month. The Foundation in St. Paul covers the entire state, and they have contacts in the Twin Cities, St. Cloud, Duluth, Rochester, Fargo, and a few other area in Minnesota. http://www.epilepsyfoundationmn.org/calendar.aspx


The Gateway City Epilepsy Support Group in St Louis This is intended for adults and older teenagers who would like to discuss Epilepsy and how it affects them. Bring a family member along with you, we would like to see many people there!  1809 South 8th Street St.Louis, MO 63104. (Held at the gymnasium next to the church.)


The Nebraska Medical Center Support Group’s mission is to provide hope and knowledge to epilepsy patients and their family members. Sessions may include educational information and resources, expert speakers on epilepsy topics and time for participants to talk, share their experiences, validate their struggles and celebrate their triumphs. http://www.nebraskamed.com/Neuro/Epilepsy/Support-Groups


Sunrise Hospital, Las Vegas. The Nevada Neurosciences Institute at Sunrise Hospital hosts a monthly epilepsy support group. This free support group is held on the second Wednesday of every month at 5:30 pm. in the Sunrise Hospital auditorium.

Dr Bangalore, an epileptologist, and one of his nurses is responsible for getting the group started. The meetings are adult oriented and range from new information regarding seizures treatment, new meds, or simple chit-chat among each other. We are a very close group and welcome all new-comers. http://sunrisehospital.com/service/epilepsy-center


The Epilepsy Foundation Massachusetts, Rhode Island, New Hampshire and Maine provides support for various groups, including: Adults, ages 18 and over, and teens, ages 15 – 19, living with epilepsy. They also provide a Parent and Family Support Network. Included under this umbrella is a Cape Cod Adult Support Group, Rhode Island Adult Support Group, Portland, Maine Adult Support Group, Boston Adult Support Group and a Post-Surgery Adult Support Group. (NOTE: Call 617-506-6041 x19 to confirm meetings before attending, in case of a cancellation.) http://www.epilepsyfoundation.org/local/massri/groups.cfm


The Epilepsy Foundation of New Jersey has support groups in Atlantic/Cape County, Denville, Hackensack, Turnersville, Vineland and Somerset County. They provide comprehensive support, personalized services and advocacy for individuals and their families in order to maximize their participation in society. http://www.efnj.com/content/resources/about-epilepsy/support-groups.php

Epilepsy Life Links in NY and NJ provides a comprehensive array of support and life-improvement opportunities for people diagnosed with epilepsy and seizure disorders. Their programs focus on the physical and mental well-being of people with epilepsy by promoting education, accessibility to health care, peer communication and a sense of community. They developed these programs with the epilepsy patient in mind and are accessible to caregivers and healthcare providers. Offices are located in Hackensack, NJ, Middletown, NY, Summit, NJ, Staten Island, NY, Jersey City, NJ, Second Avenue, NYC, New Brunswick, NJ, with a Veteran’s Educational Support Group in Middletown, NY. http://www.epilepsylifelinks.com/epilepsy-support-groups.php


The Epilepsy Foundation of Long Island has a Nassau County and Suffolk County Support Group. Both groups are run by clinical social workers who specialize in treating people with epilepsy. Groups meet on a monthly basis. http://old.epilepsyfoundation.org/local/efneny/index.cfm#.USprrjDql8E

The Capabilities Programs and Services in New York State and Northern New Jersey’s goal is to improve one’s quality of life and assist in reaching each people’s optimal level of independence. Their services are provided in either your own home and within the community. They include: Service coordination, consumer independence, basic organization and planning, budgeting and financial issues, vocational services, counseling, education and training, along with a myriad of other services. Their main office is in West Nyack in Rockland County with other offices in Middletown, Orange County, as well as all seven lower New York counties of Dutchess, Orange, Putnam, Rockland, Sullivan, Ulster and Westchester, plus Northern New Jersey. http://www.essny.org/resources.html

Peconic Bay Support Group meets the 2nd monday of every month, 7-8 pm at Peconic Bay Medical Center in Riverhead NY.

The Epilepsy Foundation of Northeastern NY serves 22 counties including Albany, Clinton, Columbia, Dutchess, Essex, Franklin, Fulton, Greene, Hamilton, Herkimer, Jefferson, Lewis, Montgomery, Rensselaer, St. Lawrence, Saratoga, Schenectady, Schoharie, Sullivan, Ulster, Warren, and Washington county. Their wide variety of programs are tailored to children, adults and their families. http://www.epilepsyfoundation.org/efneny/

The Richmond University Medical Center in Staten Island was formed to meet the needs and concerns of children, adolescents and adults whose lives are complicated by seizures and medication side effects. They have added Epilepsy Life Links, a group of programs offering assistance to patients and community members with epilepsy. Support includes: Case management/patient advocacy, educational advocacy, employment advocacy, free seizure recognition, plus first aid training and veterans’ support groups. http://www.rumcsi.org/main/EpilepsyCenter.aspx

The Epilepsy Foundation of Rochester-Syracuse-Binghamton, NY, has chapters in the following counties: Broome, Monroe, Oneida, Onondaga, Tompkins county and Ithaca. Support groups provide opportunities for sharing feelings, problem-solving and networking with individuals in similar circumstances. http://www.epilepsyuny.org/supportgroups.htm

The Capabilities Adult Epilepsy Support Group in Rockland County, West Nyack, NY maintains an environment where adults with epilepsy and parents of children with epilepsy can talk freely about their problems and rejoice about their solutions. Refreshments are provided. http://www.efsny.com/resources.html


Charlotte, NC Epilepsy Support Group. Programs may consist of an educational topic, networking to improve the quality of life for people with epilepsy, discussion groups, or social activities. The meetings are interactive and are aimed to improve the quality of life for people with epilepsy whether they are a patient, caregiver, friend, spouse, partner or parent. http://www.epilepsycharlotte.org/


The Epilepsy Foundation of Central Ohio Support Group encourages people with epilepsy, their spouses, partners and parents to attend. In addition to informal sharing of experiences, the support group also provides epilepsy education and discussion of important related issues – such as medication assistance programs, health insurance, drivers’ licensing – all of which can have a major impact on the quality of each person’s life. http://www.epilepsy-ohio.org/adult

The Epilepsy Center of Northeast Ohio in Lake West is open to adults with epilepsy and their friends, caregivers and family members. Support group sessions will include discussion and learning from one another with occasional guest speakers. http://www.epilepsyinfo.org/Services/SupportGroups.shtml

The Epilepsy Center of Northwest Ohio offers many teen, family and individual support groups throughout a 13 county coverage area. There’s a Family Support Network, Family Camp, Living With Epilepsy Seminars and a Resource Center with media related to epilepsy. http://www.epilepsycenter.org/community.html

The Epilepsy Foundation of Western Ohio Education and Support Groups is unusual in that it includes meetings for Men and Epilepsy, a Young Adult Group and Parents of Young Adults Information Group. http://www.epilepsyfoundation.org/westernohio/groups.cfm


The Gettysburg PA Area Epilepsy Support Group, sponsored by Gettysburg and York Hospitals, offers patients the opportunity to talk and gain encouragement from meeting with others who have epilepsy. http://www.wellspan.org/body.cfm?id=873

The Epilepsy Foundation of Eastern PA Support Groups offer adults, children, parents, friends and family members an opportunity to share emotional support while gaining information and knowledge. Speakers are an important component to the support group process. Groups meet in Bucks County, Center City, Hazelton Area, Lancaster County, Monroe County Lehigh Valley and Wilkes-Barre/Scranton. http://www.efepa.org/programs-and-resources/support-group-activites/

The Epilepsy Foundation of Western/Central PA, has support groups to meet other people in your local area who are also coping with epilepsy. The groups offer socialization, friendship and learning. They are open to anyone with epilepsy or a seizure disorder. Spouses, significant others and friends are also welcome to attend meetings. The groups often invite speakers to address concerns such as legal rights, medication, self-esteem, driving, employment, family dynamics and housing. There are support groups in Altoona, Hershey, Johnstown, Pittsburgh, and York. http://www.efwp.org/programs/programs_10_f.shtml


South Carolina Advocates For Epilepsy (SAFE) in Charleston are patients, family members, caregivers and friends that want to help raise epilepsy awareness in South Carolina. Their mission is to ADVOCATE on behalf of patients and their families/caregivers; EDUCATE people from all walks of life about epilepsy and seizure first-aid; INSPIRE patients, families, caregivers, students and community members to make a difference for themselves and others who deal with epilepsy on a daily basis. http://www.scepilepsy.org/#/support-group/456-221-8404


The Epilepsy Foundation of Middle and West Tennessee has support groups in Dyer County, Memphis and Shelby County, Nashville, Madison County and Cookeville. Their mission is to ensure that people with seizures are able to participate in all life experiences and will prevent, control and cure epilepsy through services, education, advocacy and research. http://epilepsytn.pmhclients.com/index.php/support/


The Epilepsy Foundation of Central & South Texas support groups discuss problems of daily living: insurance, jobs, medical care and other issues. The group is designed to provide peer support, information sharing and discussion of common interests. They may also include presentations by professionals on topics of interest. Groups meet in Austin, Pipe Creek, McAllen, Brownsville, San Antonio and Temple. http://www.epilepsyfoundation.org/local/efcst/groups.cfm

The Epilepsy Foundation of Houston/Dallas — Fort Worth/West Texas introduces you to others who understand and share your experience and give you a forum for learning about resources, exploring options, and making new friends. http://www.eftx.org/support.htm


The Epilepsy Foundation of Virginia Support Groups includes locations in Roanoke, Winchester and South Hampton Roads in Virginia Beach. EFVA ‘s mission is to promote awareness about epilepsy and provide assistance to those with the disorder. The Epilepsy Foundation of Virginia programs include two help lines, five regional offices and over 10 peer counselors statewide. https://www.epilepsyfoundation.org/local/virginia/groups.cfm


The Epilepsy Foundation Northwest Washington. You’ll find networking and support groups in Anchorage, Seattle, Spokane, Portland Tacoma and Vancouver, plus Coos Bay (Oregon). http://www.epilepsynw.org/programs/education-and-networking-groups


The Huntington, West Virginia Outreach Program, offers support services and epilepsy awareness to those in need. So far, this new support group has met with school nurses in two districts, and has teamed up with Mark Stecker, MD, a neurologist known nationally as an expert in the diagnosis and treatment of epilepsy. Future plans involve addressing transportation issues to and from epilepsy appointments, continued community education in schools, police, fire and EMTs, and counseling in local clinics. http://caudillwebsolutions.com/cincinnatiepilepsy/huntington-west-virginia-outreach.php


Epilepsy Foundation — Heart of Wisconsin. Locations: Wausau, Green Bay, Antigo, Wisconsin Rapids, Appleton-Fox Cities, Stevens Point. info@epilepsywisconsin.org


The Center for Epilepsy & Seizure Education in British Columbia deals with adult issues such as: Anger, fear, and depression relating to the diagnosis of epilepsy. And employment issues regarding: Ability to maintain gainful employment, disclosure, discrimination, and socialization anxieties: sexuality concerns, alcohol intolerance, coping with drug side effects, driving, maintaining independence and the capability of maintaining parental responsibilities. Locations in Langley, BC and Chilliwack, BC. http://www.epilepsy.cc/index.php?option=com_content&view=article&id=130&Itemid=133 or Email: epilepsy.client@telus.net

The Epilepsy Association of Nova Scotia — When you call EANS you will be connected to a staff member who will listen carefully to your questions and concerns. For example, we can help you to: navigate health and social services, communicate with your school or workplace about your epilepsy, connect with supports in your community, find additional resources. Call (902) 429-2633 or email info@epilepsyns.org to speak to an EANS staff member.

Epilepsy Adult Support Group – Kitchener/Waterloo, Ontario is for people 18 years of age or older, living with epilepsy or if they are a support person for someone living with epilepsy. http://www.epilww.com/?q=resources

At Epilepsy Ontario, a menu of seizures and issues related to epilepsy can be found. From Epilepsy and Family, Children and Epilepsy, Strategy for Care, Social Relationships and more. Although not all subjects offer a support group, it’s a rich source of information. http://epilepsyontario.org/?s=support+groups&submit.x=-1368&submit.y=-2297&submit=Go

The Epilepsy York Area in Ontario serves Aurora, East Gwillimbury, Georgina, King Township, Markham, Newmarket, Richmond Hill, Vaughan and Whitchurch-Stouffville. People can meet, socialize, or simply gather to share ideas, personal stories or experiences, issues concerning epilepsy or even coping strategies with one another. http://www.epilepsyyork.org/support%20groups.htm

Epilepsy Toronto offers comprehensive support for adults with epilepsy including counseling, advocacy and information seminars. There are support groups for adults with epilepsy, professionals, pregnant and new moms, partners of people with epilepsy and a Friday recreation group. http://epilepsytoronto.org/supportgroups.php

Epilepsy York Region in Ontario, provides parent groups, adult social groups and counseling for individuals with epilepsy or caregivers of people with epilepsy. They have in-service presentations to the public, other agencies, teen weekends, schools and workplaces. Printed information is available in other languages. A resource center is also available, plus summer camps. http://www.epilepsyyork.org/support%20groups.htm

To subscribe to Epilepsytalk.com and get the latest articles, go to the bottom box of the right column and click on “Sign me up!”


  1. Too bad there’s no epilepsy and unauthorized lobotomy group,. http://www.thewhyfiles.net/mkultra4.htm#update


    Comment by hscguineapig414895 — November 2, 2013 @ 2:18 PM

  2. Hi Phylis,

    Thank you for listing the support groups for us. Most people with epilepsy do not know that there is one close to them.

    4 months ago, I found out that I have Parkinson’s Disease along with my epilepsy.

    Have you ever heard of Periodic Limb Movement Disorder? Apparently, in my research, some people with epilepsy have it. If it is a seizure, do you know the name of it?

    Your Friend, Ruth


    Comment by Ruth — November 6, 2013 @ 6:33 PM

    • Hi Ruth,

      It’s wonderful to hear from you. But not great to hear your bad news.

      Here’s a link to Periodic Limb Movement Disorder from WebMD:


      Periodic limb movement disorder (PLMD) is a sleep disorder characterized by rhythmic movements of the limbs during sleep.

      The movements typically involve the legs, but upper extremity movements may also occur.

      Movements occur periodically throughout the night and can fluctuate in severity from one night to the next.

      They tend to cluster in episodes that last anywhere from a few minutes to several hours.

      These movements are very different from the normal spasms, called hypnic myoclonia, that we often experience initially while trying to fall asleep.

      Look at the link Ruth for more information, which, unfortunately is not too optomistic. 😦


      Comment by Phylis Feiner Johnson — November 7, 2013 @ 2:26 PM

  3. Hi Phylis,

    Thank you very much for the information. Now I know why I sleep so much during the day. I will ask my neuro for the test.

    The article also suggested avoiding chocolate, tea/with/caffeine, and soft drinks.

    Now that I think about it, when I eat chocolate and caffeine that has aggravated it. In fact, hubby was not able to stop it. You can press on the nerve in the joint of the arm and stop it. It is called a trigger point.

    I am on medicine for Parkinson’s disease.

    I am taking Sleepy Time tea, Chamomile tea and lots of Potassium. The best source is orange juice. I am getting severe foot cramps. Potassium is great for cramps.

    My father-in-law died of Parkinson’s. I know the outcome.

    I am trying to think Positive and face this challenge like I have my other health problems. I have only had it for 4 months now.

    My faith in Jehovah is helping me now. I have to get stronger. I will!! 😉


    Comment by Ruth — November 8, 2013 @ 6:41 PM

  4. EPILEPSY FOUNDATION HEART OF WISCONSIN Locations- Wausau, Green Bay, Antigo, Wisconsin Rapids, Appleton-Fox Cities, Stevens Point. info@epilepsywisconsin.org


    Comment by Dave Elmergreen — September 6, 2014 @ 8:15 PM

  5. Ed, I can’t thank you enough.

    First of all, as you saw, we had no support groups listed at all for Wisconsin.

    Secondly, this will be a valuable resource for all those who live there.

    Thanks again!!!


    Comment by Phylis Feiner Johnson — September 7, 2014 @ 11:35 AM

  6. Hi Phylis, I would like to add The Epilepsy Association of Nova Scotia to your list of support groups. Not only are they a fantastic group, but Cassidy Megan is the founder of Purple Day, and is a great asset to the group.
    If you are in Nova Scotia check it out. Great for patients, family, and friends. http://epilepsyns.org/events/


    Comment by Donna Jones — September 12, 2016 @ 12:07 PM

  7. Hi Donna, I just added it and took the info from the website. I hope I got it right.


    Comment by Phylis Feiner Johnson — September 12, 2016 @ 1:05 PM

    • Thank you! It’s perfect. 🙂


      Comment by Donna Jones — September 12, 2016 @ 1:43 PM

  8. Thank YOU Donna for the addition!


    Comment by Phylis Feiner Johnson — September 12, 2016 @ 1:48 PM

  9. I have had my seizure’s for 50 years right now. And I haven’t found the right medication that will help stop my seizures at all. I also have a V.N.S system inside of me to help stop my seizures.but it’s not helping that good at all.I am looking for something new to try


    Comment by Kenneth Gray — October 17, 2016 @ 7:54 PM

  10. You might consider the Aspire. It’s a new generator for the VNS Therapy® System.

    The new generator offers the ability to provide automatic stimulation in response to increased heart rate, in addition to its other stimulation timing.

    AspireSR® expands the use of VNS Therapy to a new responsive type of stimulation.

    VNS…Exciting News!



    Comment by Phylis Feiner Johnson — October 18, 2016 @ 9:20 AM

  11. If you live in Kentucky and considering surgery, epilepsy surgery friends have now started a group dedicated to support anyone considering surgery in Kentucky. https://www.facebook.com/groups/Kentucky.epilepsysurgeryfriends


    Comment by Anthony Williams — September 13, 2017 @ 7:23 AM

    • Thanks. That’s valuable information for all of us.


      Comment by Phylis Feiner Johnson — September 13, 2017 @ 8:44 AM

      • If it works well, Epilepsy Surgery Friends will want to start more similar groups across other states so sufferers considering surgery can connect easier with more local sufferers and information. All Epilepsy Surgery Friends need is dedicated volunteers to help run the groups like Kentucky a already has.


        Comment by Anthony Williams — September 17, 2017 @ 3:43 AM

      • Perhaps one could get volunteers through hospitals. That’s how our support group started.

        How did you start? You’re definitely an inspiration to us all.


        Comment by Phylis Feiner Johnson — September 17, 2017 @ 9:20 AM

  12. Hi please read this which tells you how we started:


    Comment by Anthony Williams — October 23, 2017 @ 4:26 PM

  13. I’ll look out for you Phylis, If anyone wants to help us promote the group we can send you our artwork to have your own items made to inspire even more with ideas we haven’t thought of 👍👍👍


    Comment by Anthony Williams — October 24, 2017 @ 3:14 AM

    • Thanks for the offer, but Epilepsy Talk is a one woman show. I don’t even have the capacity on my template for artwork!


      Comment by Phylis Feiner Johnson — October 24, 2017 @ 8:57 AM

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    About the author

    Phylis Feiner Johnson

    Phylis Feiner Johnson

    I've been a professional copywriter for over 35 years. I also had epilepsy for decades. My mission is advocacy; to increase education, awareness and funding for epilepsy research. Together, we can make a huge difference. If not changing the world, at least helping each other, with wisdom, compassion and sharing.

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