From: dbmat-bounce@xxxxxxxxxxxxx [mailto:dbmat-bounce@xxxxxxxxxxxxx] On Behalf
Of Denitral Rideaux
Sent: Sunday, August 09, 2015 7:30 PM
Subject: [dbmat] Re: Just a little farther down the road
Thanks for sharing and giving us hope. I am like you were scared to let them
fly and have their wings
Sent from my iPhone
On Aug 9, 2015, at 6:48 PM, Caroline Daley <carolinedaley@xxxxxxxxxxx
<mailto:carolinedaley@xxxxxxxxxxx> > wrote:
So fantastic to read such a glowing review! We are about 15yrs behind you guys
but I can't tell you how much we hope and pray that ms Gay is running her
amazing program when the time is right for us!
Congrats!!! You guys did it!!!
Hugs from those who find inspiration in your story,
Paul, Caroline, Lauren, Elizabeth & Jack
Sent from Outlook <http://taps.io/outlookmobile>
On Sat, Aug 8, 2015 at 11:30 AM -0700, "VIVECCA HARTMAN"
<hartmanfam28@xxxxxxxxxxxxx <mailto:hartmanfam28@xxxxxxxxxxxxx> > wrote:
That is BEAUTIFUL!
We certainly fear the same and have much uncertainty about the future as well!
Here in Houston we have a large concnetrqation of deaf-blind individuals
approaching adulthood, but have to "Hands-On" facility in place here. We are
exploring options...but notreally sure what will pan out...
For our Christopher he still has 4 more years of school, but time flies!
I will say, that having more deaf-blind education available for those who work
with our deaf-blind family members has certainly improved Christopher's ability
to interact in a more healthy manner has thos around him and has improved his
quality of life. The more education and the earlier on that we get it imposed
in our children's lives and environments the better they will do and it will
open more options for them for the future as well.
Keep doing what you are doing DBMAT ~ grating scholarships and advocating for
our deaf-blind loved ones ~ THANK YOU!!!
Much love the Hartmans
On Friday, August 7, 2015 8:43 PM, Kathy Crittenden
<dmarc-noreply@xxxxxxxxxxxxx <mailto:dmarc-noreply@xxxxxxxxxxxxx> > wrote:
I only hopes child is as successful some day soon. My daughter is Ana and I
was told she could not live in a group home due to behaviors. I don't what the
future holds for us. Thank you for sharing
Sent from my iPhone
On Aug 7, 2015, at 7:20 PM, fanfam@xxxxxxx <mailto:fanfam@xxxxxxx> wrote:
Hello DBMAT friends and family. This is Leslie, mother of the Famous Fansler
Family. Some of you have known our family, and my son Preston, for a long
time. Preston was born deaf and blind. He is 27 now; yes, Peter Pan grew up
without his mother’s permission. We have been associated with DBMAT for many
years. Each chapter of Preston’s life has brought unique challenges, deep heart
ache and immense joy. Preston has turned out to be quite a remarkable young
man. I always thought I would keep him home, with me taking care of him, until
I finally died! However, because Preston is who HE is, since graduation from
high school, he has shown me that HE wants a new chapter in his life. HIS life
plan does not include sitting at home stemming, juggling care givers while I
work, searching for ways to keep him active, hours, days, weeks of nothing much
to do, while trying to maintain the skills he worked so hard to master. HE
does not want to sit in a rocking chair while everyone around him is living a
life. Once again, I had to understand HIM and put HIS wants in front of my
unbelievable fear of the unknown and what could happen to him. There are
things about Preston’s life that scare me so badly I can’t function when I
think about them. Preston is severely disabled, but Preston is not scared. HE
wants to live, not be protected from all life has to offer. So in an amazingly
horrific, heart rending, heroic effort, unbelievable to me, these past two
years I have searched for an adult life for Preston. Scary as all get out! I
had to make sure that he would be OK plus live a fulfilling life. And guess
what….I found it!
It is called HandsOn, in San Antonio, Texas. Headed up by a lady I have know
for over 20 years, the very wise and wonderful, Gay Bellamy. It is a deaf
blind specific program. They totally operate on DeafBlind: environment, time
and activity, and those of you who have a family member understand what that
means. Preston has lived there about 6 months now. I recently visited him at
HIS home. I braced myself for how bad it would be, even though I receive
weekly reports, pics and videos, I was sure he was just not functioning at all.
How could he be, if I wasn’t there every day? I knew beyond a shadow of a
doubt that he would be frustrated, have lost many skills, unable to communicate
with anyone, have beard stubble on his face, losing weight, unable to walk
around in the house, have no recreation or daily purpose, stemming all the time
and ready to come back to his mom and family home. Well, that just wasn’t
reality. Preston is AMAZINGLY happy. He has gained skills and weight. He
showed me his room, and was proud of it. He knew all the routes in his house.
He was busy, busy, busy and not stemming. Dare I say it….. he ACTUALLY
communicates with people. But the best part, Preston has a friend, not a paid
care giver, but a deaf blind peer. Preston has a friend. Who would ever have
believed the impossible dream could come true?
As I headed home from San Antonio I felt like I could breath again. Preston is
living HIS life plan. Hopefully this posting will give those of you, with an
adult family member, the wisdom to see that life for our guys doesn’t end at
graduation, it begins. I hope this gives you the courage to get past your fear
of being the only one able to care for your adult family member and the
unknown. And I hope it motivates you to look at HandsOn’s website at
http://www.handsonsa.org <http://www.handsonsa.org/> Contact them and see
their program. Mostly, I pray, that we all understand life is worth living.
Preston is LIVING. Go my sweet son, we gave you roots to grow, and now, it is
such a precious gift to watch you bloom.