A Common Voice Planting The Seeds Of Hope!


Home

Contact / Jobs

Parent Partners

Articles / Links

Testimonials

Newsletter

Support Groups

Donate

 

 

A Common Voice is a parent driven, nonprofit organization funded by Washington State Mental Health. Our goal is to provide support, technical assistance, and to bring Pierce County parents together who have experience raising children with complex needs.  We pride ourselves on building a partnership between, Communities, Systems, Families and Schools.

 

Testimonials & Letters of Support

5-30-2006

TO WHOM IT MAY CONCERN;

My name is Kerstin Metzger, are and I am raising an adopted son, his name is Kristof. He is now eleven years old. When he was eight years old, he was diagnosed with Asperger Syndrome, which is a high-functioning form of autism.

We had suspected that he was suffering from some sort of disorder, since he was three years old. He was dicey it nosed with ADHD, obsessive compulsive disorder, oppositional defiance disorder, and intermittent explosive disorder. All these disorders only where manifestations of the autism

After quite the prolonged fight without health insurance, we finally were referred to a psychologist and a psychiatrist, who in turn referred us to a wonderful counselor, who ultimately narrowed down his autistic traits, who caused his behavior.

By that time, he was out of control, and he had plunged our family into crisis. He was destructive, impulsive, somewhat physically aggressive, and I was at the very end of my rope. I simply wanted to give up!

In September of 2004, I contacted the lady with the Autism Society Tacoma Chapter, who referred me to A Common Voice for Pierce County Parents. I immediately contacted Marge Critchlow, their director. She invited me to a support group, which was meeting every Wednesday evening in Puyallup. I would like to state from the bottom of my heart that this organization has changed my outlook on life profoundly. A common voice gave me support, hope, and most of all provided me with incredible a useful tools on how to deal with an autistic son without letting myself get destroyed.

Marge Critchlow and Sherry Lyons, the director and assistant director give advice and offer practical solution when it comes to parenting kids with a neurological and mental disorders. They speak from experience. Their experiences offer hope for the future to other parents like me.

I have made the weekly support group an integral part of my schedule. Every Wednesday I learn something that I can use in raising my son. I am a much calmer, better prepared parent now. Even when I have had a rough week with my son, I know that I can go to the support group, talk about my bad week, and receive sound advice about how to better handle things next time without ever been judged.

I am forever grateful to A Common Voice and to Marge and Sherry!

Sincerely,

Kerstin Metzger

 

 

 

 

 

 

7/2010

To A Common Voice;

I am the proud mom of three children. My oldest daughter was a typical child, wonderful teenager (is there such a thing) and lives in San Diego, CA with her husband. She gives us lots of joy from a distance. My youngest daughter was a typical child, frustrated teenager because she faced the challenges of being gifted; she received her Bachelors Degree by the age of 19 and will have her Masters Degree by the age of 21 from Western Washington University in Bellingham, WA. She also gives us lots of joy from a distance.

When my son and youngest child Jonathan was born with meningitis, I should have known he was going to be our greatest joy. The doctors told us they did not know what form or how the affects of the meningitis would appear but we will monitor him and see what life brings us.

By the time he was 2 years old, we knew he was going to be a challenge when the doctor said, “I’ve never diagnosed a child of 2 with ADHD and ODD severe but that’s my diagnoses for your son.” Being naive to the mental health world, I asked for a treatment plan for him, the doctor told me “we don’t do anything - we can consider medication but not until he was at least 3 years of age”. By the time he was 3 years of age, I knew one of us was going on medication, him or me.

Jonathan has been on various medications and his diagnosis has changed going as high as five mental health disorders; but just last year we landed on the Asperger Syndrome, which is a high-functioning form of autism. We have been very successful working, as a team with his med’s doctor and therapist on his positive behavior modification plan.

Jonathan has struggled in various school environments because of his disabilities and our relocating him every 2 years due to his family being in the military. I have lots of experience with different school settings; personnel; successful IEPs, FBAs, and Positive Behavior Plans. His dad retired 5 years ago so we have been able to settle him down into one school district (system) which has been instrumental in his progress.

We have struggled along with him, learned school systems, treatment plans, and have been the parents of THAT child. We felt so alone and at times like the biggest failure as parents! Jonathan’s therapist told us to consider attending a support group so we did not feel so alone plus could assist other families with our knowledge. We attended our first Y.E.S. Support Group in Puyallup and walked away with huge (and I mean huge) feelings of acceptance and parent support!

We have provided support for Jonathan through the years and now we have our OWN support system, where we are not judged and nobody is shocked at what comes out of our mouths! The people there are walking in our shoes or have walked in them. They understand how we feel sometimes without us uttering a word. Just ask anyone, we have the meetings on our calendar and it is a priority for us! It is something we do for us as a couple as well as for our family. We handle LIFE differently now and feel empowered and not alone because of our support group.

Forever Grateful,

Ronda Fullerton