Her tired hands are soaked in soapy water, going through the
motions of washing a pile of dishes that never seems to end. She can barely
keep her eyes open, but she knows there will be several more hours ahead until
she can attempt to fall asleep. More than likely, she will get very little
sleep. Just like the night before…and the night before that. The kids still
need to eat dinner, finish their homework, and get their baths done until
negotiations for bedtime will come. She has to make sure that her youngest
child has her own time to wind down and follows a specific routine or she will
get very upset, having been diagnosed with Autism at the age of four.
Plastered across the refrigerator space, there is hardly any
room for colorful drawings or family photos because of all the different
schedules that have now become the blueprints for their new life. Appointments
with the TBI doctor, the husband’s therapist, the children’s therapist, the VA
clinic, and the Autism support group are all color coded so that the children
know what to expect this week. The woman
looks at the refrigerator with her tired eyes, and feels a tug in her chest
knowing that soon she will have to tell her son that he can no longer go to his
guitar lessons because she can no longer afford to pay for them.
Suddenly, she hears the familiar sound of a truck door
slamming shut, and anxiety increases the tightness in her chest. Her heart rate
quickens, and her fatigued muscles are now tense with expectation. What kind of
mood will he be in today? Now, she can hear the back door to the mud room
slamming shut and a curse of impatience from her husband as he trips across her
daughter’s tennis shoes, left haphazardly thrown in the doorway when she came
home from school.
The children all run eagerly into the kitchen, excited to
tell their father what they did at school that day, who said what, and asking when
he can play outside with them. Rather than greeting his children with a big
smile and open arms, he rubs his face in agitation and pushes them aside. The
children are hurt, but know that their Daddy must need his quiet time. It’s
best just to leave him alone, but they can’t help but wonder when their Daddy
will be better again. All they know is that their father went away for a while,
and came back a different Daddy…a Daddy that doesn’t want to play with them
anymore and yells at them when they get too noisy. The old Daddy loved to go
out on family trips and have fun, but now he takes lots of naps and says
everything is too loud or too bright.
The woman at the kitchen sink fights back her tears,
thinking of how her husband used to kiss her when he came home every day, and
how he would stay up talking with her at night about the children, laughing
over funny memories. Now, the man that returned is more like an empty shell of
a person…an angry roommate rather than a husband or father. She wants to help him so badly, but doesn’t
know what to do. Her family and friends all mean well, but they just don’t
understand what she is going through…and she feels guilty about asking for
help. She knows that something needs to change, but doesn’t know how to make it
happen.
This is an example of the daily life of some military
caregivers. Across the United States, we currently have 275,000-1,000,000
military caregivers. But what is a military caregiver? According to a recent RAND survey, a military caregiver is a family
member, friend, or other acquaintance who provides a broad range of care and
assistance for, or manages the care of, a current or former military service member
with a disabling injury (physical or mental) that was incurred during military
service. The culture of military caregiving is unique because these caregivers
are dealing with multiple and severe injuries or illnesses, a very complex
system of care (VA/Tricare), and invisible wounds such as Post Traumatic Stress
and Traumatic Brain Injury. What also sets them apart from other caregivers is
that many of them provide around the clock care or feel as if they are “on call”
24/7, and will continue to provide a lifetime of care to their loved one.
Out of our service members deployed during Operation Iraqi
Freedom and Operation Enduring Freedom, at least 725,500 returned home with a
Traumatic Brain Injury, PTSD, or depression. The families and spouses of these
service members are stepping up to the plate and filling the dutiful role as
caregiver before ever knowing what they are truly facing. The role of
caregiving often affects every aspect of a military caregiver’s life. According
to RAND, the roles and responsibilities of caregivers often take more time than
holding a typical full or part-time job. In a survey of veteran caregivers by
the National Alliance for Caregiving, approximately one-fifth provided more
than 80 hours a week of care, and more than two-thirds (69%) provided more than
20 hours of care per week, leading some caregivers to experience a decline in
their own health and well-being. As a result, some military caregivers have
extensive needs, independent of the needs of their loved ones.
Military caregivers in particular suffer from mental health
issues at rates greater than the non-caregiving population, with one study
showing about two-thirds suffering from type of emotional stress.
Unfortunately, resources for this group of caregivers are often challenging and
limited. Military caregivers cope with the ongoing challenge of caregiving
itself while sorting through a maze of policy structures, program
opportunities, and well-wishers to meet both their own needs and the needs of
their veteran. These efforts are not always successful. A large gap between
caregiver needs and community resources have yet to be met. The RCI’s Operation
Family Caregiver program seeks to help accommodate the needs of these
caregivers and provide the training and tools necessary to help relieve their
burden and stress.
Operation Family Caregiver provides free and confidential
support via in-home sessions, Skype and telephone for military caregivers who
want to be proactive in learning how to effectively identify and solve the
problems they are having as a result of their loved one’s injuries. A program
coach works one-on-one with the caregiver in a research-based, customized
training approach that empowers the caregiver, allowing them to feel more
confident and less stressed about taking care of the needs of their loved one.
Reaching out for help is a sign of strength! Call today to
schedule a free assessment: (229) 931-2034.
Hi Mandy - I am Sarah, I am the wife of a 5 time Iraq veteran who was wounded in 2007. I am also a mother to 3 little blessings - 1 of whom is Autistic, and another we thing may have Aspergers.
ReplyDeleteThis post was absolutely beautiful, and really hit home for me :)
Thank you so very much for sharing :)
http://www.sarahbowley.com/
I am so glad you enjoyed it, Sarah. I find it very interesting that at least three of the military families I have worked with have at least one child with special needs, most of them having a child with Autism or Aspergers.
DeleteMy background lies in education, and a large piece of my heart belongs to those students with Autism. They were some of the most unique and fascinating kids I've ever met :)
Please let me know if you ever need any resources or may be interested in our program. We'd love to have you participate!
Blessings and love,
Mandy
I read your post and saw myself....minus the autistic child (my son has ADHD/ODD and my daughter has epilepsy/asthma). It seems when it rains it pours on us as caregivers! I am excited to look into your program!
ReplyDelete