Support Groups

Support Groups

There are “too many to count” types of support groups. Within the area of stuttering they come in many different flavors. For example, some actually do therapy-type exercises, while others see it as a time to feel comfortable about being personal about their stuttering, and some have a variety of activities such as guest speakers and informational topics, etc.

Therefore, anyone forming a group must think about who should be part of the group. It seems the most common group form is that of adults (with age defined by group leaders); however, parents feel a need to get together as well as for their children who stutter, to have somewhat structured time together.

Some groups request a fee or donation, while others are free. Which of these motivates consistency in attendance? This is a valid question.

Many individuals feel they need not respond to individualized (electronic) announcements, but rather prefer to attend as they can. Well, I have a problem with no RSVP, but do feel there should be freedom to attend at will or according to need. Your thoughts?

It is known, however, that at least for local stuttering support groups their longevity is short, relatively speaking (I believe the average is 2½ years). When numbers dwindle but the leaders are faithfully there with plans (and space, and their time), I think everyone becomes frustrated. Many people have shared with me their experiences of finally giving up the group’s existence, but that seems unfair to those who continue to need them.

Perhaps you can respond as to what you have done or experienced. The group that I and another person facilitate (for adults) has been in existence for five years. We’re searching for fresh ideas and I’m sure other group leaders/facilitators are as well, so we can all benefit by sharing.