Lil Miss Maegan   ON THE WORLD WIDE WEB

About Lil Miss Maegan
(or bits and pieces that make up the person behind the Lil Miss)


 

Artist's Bio:
Born overseas to a diplomat, raised and educated in Virginia, Maegan Lowrey studied photography at Barton College.  In 2006 she joined the Creative Expressions Studio program at the Arc of High Point.  Since then her artwork has received top honors in competitions.  Maegan Lowrey resides in Greensboro North Carolina and enjoys computers, music, visiting with friends and photography.

SelfAdvocacy & Reaching Out:
"I love to volunteer and help others, especially adults with developmental disabilities.  I am the Past President of the High Point Aktion Club.   Aktion Club is sponsored by the Kiwanis Club and is a great way to help the community.   Our club began as a self advocacy group within the Arc of High Point.  We grew so big that we joined another group called ONE VOICE.  We received our charter from The Kiwanis Club in 2009."

The High Point Aktion Club meets on the First Thursday of each month at Emerywood Baptist Church.

           Check out the OneVision-Aktion Club's Site


The Arc of High Point is non-profit organization that supports and advocates for adults and families who have children with developmental disabilities. 

Lil Miss Maegan presenting at a disability awareness fair at Oak Hollow Mall
 
Please support the Arc of High Point

 
To Volunteer is Another way to give back to the community.
 

 

 About my disABILITY
"When I first moved to Greensboro I lived with my sister (Kathleen) and she wanted me to be more independent.  I was having trouble finding work, taking on my responsibilities, and being physically active.  She really cared about my well being and was concerned that I wasn't "growing up".  She thought that I might have a disability.  So my sister did some Internet research on disabilities.  She typed in my -characteristics- "born with  short stature, small hands/feet, and conjoined toes."   I also had to have hip surgery when I was about 12.  My sister  also looked into behaviors.   She suspected some form of autism and I  do have some characteristics of ADHD.  Kathleen search had  found  the CdLS Foundation's web site.   They provided a local contact for Duke University.   We arranged for an appointment with Duke University.  We needed a "medical diagnosis" to receive services from Vocational Rehabilitation and the Arc of High Point.  We went to Duke University, where I was diagnosed with a mild form of Cornelia de Lange Syndrome."


"Because I was diagnosed so late (at 28 yrs old), my family always had “normal” expectations for me. I also had the same kinds of hopes.  Finding a job, living in my own apartment (not living with my parents), and having meaningful friendships.  Now I have a better understanding of why I reacted that way, or did this or that.  I don't always go to the doctor or take medications.   I don't like making phone calls or refilling medications.  I understand that phone calls and appointments  are important.  I am very shy on the phone, but not in person.  So I usually have to go in person to make an appointment or get medications.  Because of the hip surgery, I could never run or do high intensity workouts.  This does prevent me from doing any heavy lifting in a work setting.   Working with VR, they know all of this, so they help me find the right kind of work.  I also receive “supportive employment” –which is really helpful. (I don't just quit) I have someone to help out with my on-the-job anxiety."
 

What is Vocational Rehabilitation?
Vocational Rehabilitation is State Supported program designed to help persons with disabilities find and keep employment.
There are a few vendors and agencies that work with the State VR.  (not endorsed here, but a list of agencies that I have worked with).  The VR program also participates in the CAP (Client Assistance Program).  If you are not satisfied with the performance of your VR staff you may call North Carolina  CAP office and they can assist you.   You can also "switch" vendors or offices.

Please contact your local office

  My Partners Experience
"Sometime after moving to Greensboro my sister and I began attending the Mayor's Committee on Disabilities   I met a woman named Dotty Neely, who also worked on the Barriers Committee.   Dotty suggested that I apply for a program called "Partners in Policymaking".  At first, I was anxious and didn't want to participate.    However, I decided to make application for the program.  What a life changing experience (so glad I did it)!  The program lasts about 8 months and it is made up of seminars, presentations, and training.   Some of the subjects covered are:  inclusion, employment, advocacy, and legislation.I am a 2005 graduate of North Carolina's program."

Partners in Policymaking is a leadership training program designed for adults with developmental disabilities and parents with children with developmental disabilities.   It is a national program that was created by the Minnesota Governor's Council on Developmental Disabilities, in 1987. 

Want to learn more about Partners In Policymaking?
Click on the link to the right 


North Carolina Council on Developmental Disabilities


and now for something compLetely different....


 How to have fun and enjoy life in "G-boro"


 
AT HOME
AROUND TOWN
FUN LINKS
playing games.....

instead of cleaning
Elm Street


Videos


  YouTUBE

"minor adjustment"

"ZAP!"
City Park
DEATH METAL POLKA

no...really there is such a thing
(google it!)
COMPUTER GRAPHICS
PC & MAC
Looking North-East

FACEBOOK & MYSPACE
summer FESTIVAL
THE ONION

 
Up to Advocacy & Support

 

Art-in-a-Cart  "COMING SOON" to a Craft Market Near YOU!
Artwork for Sale
 
 
 
 

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