Spring 2006 Newsletter   click for links to other newsletter pages
From Our Director
Steve Mason, Executive Director

There are many themes that could be selected from the feature story in this edition of The Heart of It, but few as compelling as the subject of “self-advocacy.” 

By most accounts, self-advocacy rarely if ever occurs through the actions of a person acting alone, even though the word “self” suggests otherwise. Most often, self-advocacy is achieved through independent groups of people working together to achieve a common goal, like recognition and the attainment of certain rights.

While it certainly can be said that Samantha Henault, the young woman featured on the cover story, is an excellent self-advocate, it can also be said that she spends most of her time in that role working within groups of people with the same interests. Samantha has learned about advocacy from the best of the best, her family. Sharon and Bernie Henault are not only Samantha’s grandparents and guardians; they demonstrate advocacy and leadership in all they do for their communities in the Northeast Kingdom.

As noted in the cover article, KASA is an organization sponsored by Family Voices (Parent to Parent of Vermont is the Vermont affiliate of Family Voices). Samantha is able to advocate through this national, grassroots network of youth with disabilities (and their friends), by speaking out. KASA members are leaders in their communities, and they spread helpful, positive information to increase knowledge around various issues. Those issues include: living with disabilities, health care transition issues, school, work, and many more.  All this is able to happen only because KASA is an available resource.

We at Parent to Parent of Vermont believe it is very important for people to have options such as places to go, people to meet with, and things to do.  Some people often take these basics of community interaction for granted, but to many, these are choices that only come after much hard work.

We advocate for families with children who have special needs. This is a particularly essential endeavor because Parent to Parent of Vermont is a family-centered, peer support organization – as such, we function as an advocacy organization and as a self-advocacy organization. Put another way, we strive to give others options to advocate (see under Family Voices and Support Groups, for example), just as many choose to take advantage of opportunities to self-advocate. (We also encourage you to join our Listserv.)

As a Vermonter, I am often struck by the many options we have as citizens. Options like parks, lakes, hiking trails, town and county fairs, parades, turkey dinners - even our legendary town meetings - are just a few examples of ways Vermonters can connect with their community.  And if your options are dictated by the weather, you are particularly lucky to be in Vermont.  If the weather isn’t right for the option you chose, you need only wait until tomorrow when the weather may be exactly the option you desired.  Most of us have learned, however, to choose our options according to the weather we have that day.

Lastly, just having options available is not always a panacea.  Can we get to where we want to go, does the activity accommodate all participants, and will other participants welcome us?  These are the more difficult issues we face even when a choice from many selections exists.

One of Parent to Parent’s goals, expressed in our vision statement, is that families live in communities where differences are embraced. This can only be accomplished when there is an ongoing effort to advocate for inclusion. 

It is not enough that there are options in our communities. The options need to be accessible and viable. It is to each of us as individuals, sometimes acting in unison with many others through organizations like Parent to Parent, to ensure that everyone is provided with full and equal participation in all aspects of community life. In this way, all can fulfill their potential and make their dreams come true.  ©

Steve Mason

Spring 2006 - In this Issue:
Vermont Teen on National Board
From Our Director
Don't Sell My Boy Short!
Sotos Syndrome Conference
Updates
(plus 2 articles on Autism)
Ethan's Fairies
Join Our Listserv!

Heartfelt Thanks 

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