Guest guest Posted December 7, 2006 Report Share Posted December 7, 2006 Have you ever wished there was a support group for LBD caregivers in your area? If you are an experienced LBD caregiver or a healthcare professional and would like to help LBD caregivers in your community come together for support and education, consider becoming an LBD Support Group Facilitator! The Lewy Body Dementia Association (LBDA) is looking for individuals who would like to help launch a local LBD caregiver support group. This role is perfect for retirees, and part-time or former LBD caregivers. (For full-time caregivers who also wish to volunteer, we recommend co-facilitating or participating on a support group steering committee.) The requirements for this volunteer position are: • LBD caregiver experience or related professional experience like social work, counseling, nursing, etc. • A friendly personality • Good organizational skills • Telephone access, Internet access highly recommended The position requires a commitment of about 5 hours a month for one year. We will provide you with a LBDA volunteer orientation guide, a Support Group Facilitator manual, and a current LBDA Support Group Facilitator who will serve as a mentor to help get you started. If you would like to learn more about this volunteer opportunity, we invite you to join representatives of the LBDA for a teleconference call on Thursday, January 4, 2007 at 7:00 p.m. Eastern Standard Time. Please contact Ronnelle (Ronnie) Genser at genser@... to register for more information and for instructions to participate in this call. In hope, President Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 7, 2006 Report Share Posted December 7, 2006 Hi June, The reason for the teleconference on January 4th at 7 pm ET is to do exactly what you are asking – to explain the role of a Support Group Facilitator and what is involved. If you would like more information before the teleconference, call (not e-mail) me after 6 pm ET evenings or anytime on weekends at and I’ll be happy to speak with you. Otherwise, I will put you on the e-mail list to notify you of the telephone number to call for the teleconference. You sound like you would be a great support group facilitator. Thanks so much for your interest. I hope others will come forward and offer to be support group facilitators in their areas. P.S. I have facilitated a support group for ‘Adult Children of People Who Have Alzheimer’s Disease and Related Dementias’ as a volunteer for the Georgia Chapter of the Alzheimer’s Association for almost 4 years. My Mother is now in the end stage of LBD. I probably average 2.5 – 3.0 hours a month related to facilitating my group - 2 hours for the actual group meeting; maybe ½ hour/month or less taking calls of people who wish to join the group, a few minutes after the meeting faxing a sign-in sheet to the Alzheimer’s Association, and about 5 minutes once a month sending a reminder e-mail 10 days before the meeting to everyone in the group. This is really not a large time commitment, but is a wonderful opportunity to provide and get support. Some people may put in more time as a support group facilitator; that is up to each person. I’ll explain more details about the entire process in the teleconference. Regards, Ronnie Genser, LBDA Board Member and LBDA Support Group Coordinator Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2006 Report Share Posted December 19, 2006 PS -- FYI I just signed up to be a LBDA volunteer. I'm going to start small by volunteering as a Community Awareness volunteer. And should that work out and I can handle a bit more, then I'll volunteer to be a local support group facilitator (Massachusetts.) But need to know if I can handle the smaller role first. If there are other MA individuals out there too who would like to volunteer with me we can get a local group together... Quote Link to comment Share on other sites More sharing options...
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