Monday, September 1, 2014
Wednesday, June 18, 2014
Friday, May 30, 2014
Fresh Art From A Cool Cat At Spa Mosaic
Mama C. at a recent show at Gallerie Ellipsis in Newport, RI
Causey
spent most of her career working as an art teacher for elementary, middle, and
high schools students. She also moonlighted as an art director and consultant
for many galleries as she moved up and down the east coast. Now happily retired
in her native land, this forever-young spirit of the sixties has fixed her
focus on her own art, which is currently on display at Spa Mosaic in the South
County Commons until June 27.
“I
absorb myself in nature, and through this total immersion, I learn to respect
its essence,” Causey says. “When I paint, I like to
have some music going while I dance around my studio. The music shows me the
way.”
Whatever
she does to get in the moment seems to be working. Her broad range of
techniques helps her transcend boundaries, and her art has captured attention
from fans both young and old.
A
teacher is a perpetual student who never stops looking for inspiration. Though
she holds three degrees – two masters, and one bachelors - from the Rhode
Island School of Design, Causey is constantly enrolling in workshops and
courses to help sharpen her skills and expand her horizons.
On
one of her latest adventures she spent a month in Italy with renowned painter
Julian Nightangale. “It was truly amazing to be able to work in the Italian
countryside,” said Causey. “To truly soak in the landscapes of Tuscany and
Umbria, and be able to learn from someone who knew the area so well is an
experience I will keep close to my heart.”
Italian Inspiration
One
recurring theme in her body of work is the ocean. As a surfer and
paddleboarder, Causey spends a lot of time in and around the water. She says
the act of surfing keeps her mind and body in tune with nature, which opens her
eyes to inspiration. One day while boogie-boarding in Hale’iwa, Hawai’i, Causey
had an experience that helped her to begin thinking “outside the box” when it
came to her paintings.
“I
was sliding down the face of this beautiful wave when the lip pitched forward
over me. Everything went silent as I was completely covered up and riding in
the tube. With the spit on my back, I came flying out and I went crashing onto
the beach. I had the biggest smile on my face. It was so beautiful in there
that I even cried a little bit.”
Waves
The
artist tried many times to capture that moment on canvas but remained
unsatisfied with the results. That was until she decided to break the mold by
building and stretching her own canvasses into the shapes of pentagons and
hexagons. Causey explained that working with shapes closer to circles has
helped her to paint waves in a whole new way, as the circular shapes give the
paintings more movement and energy.
With
unconventional shapes comes unconventional style. Causey breathes life into her
paintings by layering oil & acrylic over spray paint, or by mixing
watercolors with strips of tinted tape for added texture.
Tape & Texture
“I’m
never afraid of failures for one can grow and learn from them” she said and
continued, “For me, creativity equals seeing more than is really there.”
Friday, May 9, 2014
Apraxia Awareness Day is Wednesday May 14
When Portsmouth resident Kendra
Jenkins’ son, Talen, couldn’t move his mouth properly to blow out his birthday
candles on his second birthday she knew something was wrong.
Jenkins was heartbroken when,
after six months of searching for an answer, her son was diagnosed with a
condition called Childhood Apraxia of Speech (CAS). But like any good mother,
she would not let this overwhelming prognosis keep her from getting Talen the
treatment he so desperately needed. But Talen’s treatments had very limited
coverage under their insurance. When he was diagnosed, Talen could only speak
ten words. “He couldn’t even pucker his lips to give you a kiss,” the mother
said.
CAS is a motor speech disorder
that becomes apparent as a child is leaning to speak. The disorder effects how
one’s brain communicates with the muscles involved in speech, making it
difficult for an affected child to plan and produce the precise, highly refined
and specific series of movements of the tongue, lips, jaw, and palate that are
necessary for intelligible speech.
Jenkins gained comfort and
determination by volunteering for the non-profit group Childhood Apraxia of
Speech Association of America (CASANA). They helped her to get Talen into the
right programs, and connected to other Rhode Island families - 50 that she
knows of - going through the same struggle. Together they have made great
strides in increasing awareness of this rare condition (approximately 1-2 per
1,000 kids affected), and last year marked the first official Apraxia Awareness
Day, which takes place on May 14.
During a Town Council meeting
Monday night, the town of Middletown unanimously voted to proclaim May 14, as
Apraxia Awareness Day for the town. This was in response to a letter written to
the council by Jenkins. She wrote a similar letter to the Rhode Island Governor
Lincoln Chaffee, who on May 14, will sign off on a proclamation for the State
of Rhode Island to recognize the day as well. A group of Rhode Island families
affected by CAS will travel to the State House to meet the governor and witness
the signing.
“I am so proud of this
accomplishment, and I would like to bring more awareness to our local
communities,” Jenkins said.
On Sunday September 14, 2014 at 9
a.m. the Walk for Children with Apraxia of Speech will be held at Colt State
Park in Bristol. A one-mile walk within the park will be followed by other
activities such as face painting, music, and raffles.
Jenkis said one of the biggest
problems with CAS is that the general public, as well as doctors are unaware or
know very little about the condition. According to Jenkins, CAS is often
misdiagnosed as autism because the child cannot speak, and sometimes is not
properly diagnosed until the age of five.
Jenkins also said CAS requires
specific one-on-one treatment and intense speech, physical, and occupational
therapy. She said that her insurance currently pays out on 24 speech therapy
visits per year. “We go through those visits in about eight weeks,” said
Jenkins.
In 2008, CASANA began funding
pilot research projects to make sure that kids with (CAS) can be properly
identified, to figure out which treatment methods are most effective, and to
learn more about the longitudinal life-span of (CAS), such as what percentage
of children – with appropriate help – end up going to college, and holding
jobs. Their work has lead to more published journal articles on treatments, and
has enabled researchers to go to the National Institute on Deafness and
Communication Disorders to fund larger projects, which include CAS.
“Not all insurance companies are
the same,” said CASANA founder Sharon Gretz. “Some cover it, some cover speech
therapy, but not enough of it, and some don’t cover it at all. We support
families by aiding when appealing denials to insurance companies by providing
materials and information to support their efforts.”
Over the past year, Talen has
attended seven speech therapy sessions a week, four at Mellville Elementary in
Portsmouth, and three at Alphabet Soup in North Kingstown where he receives
PROMPT therapy, a technique that involves restructuring oral muscular phonetic
targets. This means that the therapists physically manipulate the oral muscles
by pressing underneath the chin, around the nose, cheeks, and other areas to
help the child feel the muscles needed to make specific sounds. “The process is
very invasive, but Talen has grown to love what they help him accomplish,”
Jenkins said.
With proper treatment Talen has
gone from being able to speak 10 words to an impressive 60, and now has a vowel
accuracy rate of 70 percent, up from 10 percent when he started. Perhaps the
most heartwarming aspect of his treatment however is that on his fourth
birthday Talen was able to blow out all his birthday candles on his own.
Councilor Bruce Long thanked
Jenkins for her hard work and recalled when insurance companies were reluctant
to cover services for autism. He said after people pushed hard to raise
awareness, legislation was eventually passed mandating insurance companies to
recognize and coverer the disorder.
“That’s why were here,” said
Jenkins and continued, “The more people know about Apraxia, the more cases can
be diagnosed sufficiently.”
For more information on log onto www.apraxia-kids.org
Tuesday, April 1, 2014
Monday, March 31, 2014
Wednesday, March 26, 2014
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