Saturday, December 12, 2015

Aislinn's Treasures Pixie Dust



















Imagine a world much like a fairy tale where all things are possible.  Or perhaps a place where lotions, and potions are at the wiggle of your nose or wink of your eye.  A Universe where all you need is a faith, trust and a little pixie dust.

To some children in the organized chaos, pixie dust means a place of safety where everything else around them seems different, broken, or out of order.   It might also mean love as they feel the healing energy from various therapists or family member.  When the children are locked inside his or her own world, at last, in a brief escape could feel a sense of peace and warmth. The absolute best part is having the magic delivered by real life fairies and angels.

Pixie dust comes in all forms like...a beautiful jar, special necklace or a collection of music notes.

 
Aislinn has a real life fairy the brings blessed potions and lotions.  These blessed items might sooth a cranky spell so an x-ray can be taken or to help fall asleep. One is used as an  aide in breathing during a nasty cold or respiratory.   Another is applied to help heal broken down skin because her chariot is a wheelchair.  There is a new one to her collection with high hopes of reducing seizures.      


This is Aislinn's magic wand.  It applies her pixie dust!   Well...using key body points it actually delivers quartz crystals to cause electrical stimulation.   Its benefit is similar to acupuncture without needles and is delivered to the body in seconds!  Its called a Japanese Deluxe Piezo.  Sound unbelievable..not to me as I am seeing the benefits in Aislinn.  She is on the verge of a speech breakthrough and increased cognition.        

In our Universe there is faith, trust, and a little pixie dust.  What is your magical potion or pixie dust?


Much love,
Michelle D.  Voss-Shelley 
Mom to nine year old Aislinn living with a GRIN1 mutation
butterflyicebaby@gmail.com



Thursday, September 24, 2015

Aislinn's Treasures It Is Time To Dance



There are so many things that need doing every day when you're blessed with a child with special needs.  Some days is feels like all work and no play.  Take a peak into Aislinn's world on any given day...

We talk to angles.  

We nap with the our cat Haven, but today we have too much energy sleep the day away.

Laundry has got to be patient. There are always clothes that can be borrowed from big sister.   Besides doing laundry is BORING AND NEVER ENDING!

Look at this grass. It sure needs to be cut.  I'd rather break a sweat doing something more fun.


Dinner needs to be cooked. Why don't I order in.  The local Chinese restaurant is open holidays.  If I cook, the dishes will have to be washed by hand because the automatic dishwasher is full.  If you know me....I am likely to burn it anyway.    


Aren't I due for day off or at least a coffee break or a bathroom break?  I have heard all work and no play makes you dull.  Am I dull?    Maybe I will put my earplugs in and hum annoyingly loud.  

Do you hear that......


Amazon are you ready for my request?  Will you play something that moves my soul?  

What?!? Is that my song?  Is it time to sing....no it's is time to dance!  I am singing and dancing!!!    See what I can do despite my disabilities.   I am singing and dancing!!!  

I am still dancing!!!!


Life is good!  My soul is rejuvenated!!!   
Much love,
Michelle D.  Voss-Shelley
(Mom to nine year old Aislinn with a GRIN1 mutation)
(butterflyicebaby@gmail.com)

Saturday, July 11, 2015

Aislinn's Treasures Chicas Bonitas (Beautiful Girls)

Chicas Bonita (Beautiful Girls)


Our controlled chaos is perfect for me and Aislinn. Aislinn is fast approaching nine years old.  It is a huge milestone for her because I had been told she may never reach her second birthdate.  I am certain it is due to the magnificent individuals in her life.  Being normal used to be a wish of mine.  I have since learned there are miracles that transpire out of the abnormal.   Our controlled chaos is perfect for me and Aislinn.

If you are always trying to be normal, you will never know how amazing you can be-Maya Angelou. 
















Lately, I have been reflecting on the cycle of life.  It brought me to a place to look at the women in my life.  During this reflection, only the strong women remained in my life because their friendship and wisdom.  Each has had a part in making me into the daughter/sister/wife/mom/caregiver I am today.  Truth be told, I someday aspire to be a Nana or Grandma.  Yep…Granny is even possible and growing old is comforting to me.  I will go willingly to the next stage in life.  In doing so, I will gain more appreciation for the stages are closing behind me.

Like Grandma like granddaughter.  Like Mom like daughter.     
 

Like Great Grandma like great granddaughter.

Sisterhood by blood or by fate.
      

 

 I ran the across the following quote.  It embraces the very essence of the strong souls who have sculpted mine during in sisterhood, childhood, or motherhood.    I suppose you might recognize the same type of spirit in your tribe or village…
 


Take time to visit in the hospital, chat in the driveway, eat a homemade pizza, drink ice tea or a frosty diet Pepsi or pose for an impromptu, yet, meaningful selfie.   Take it from me the BONITA will enrich your life.

Much love,
Michelle D.  Voss-Shelley
(Mom to nearly nine year old Aislinn with a GRIN1 mutation)
(butterflyicebaby@gmail.com)


Sunday, March 29, 2015

Aislinn's Treasures Rebulid

It is sometimes difficult to find the silver lining or bright side of life when your child is terminally ill.     It is even more difficult to find time for the other loved ones in your life.  

I really thought I was on top of everything.  That was until my house of delicate cards came crashing down.  Aislinn had surgery, she was then re-hospitalized for uncontrolled seizures, all family members got very sick with pneumonia, the holidays were unfolding, a large acquisition at work took place, and there was a breach of professional boundaries.  

No body can give you the tools to overcome all of the events at once.  I was lost and broken.  Where was my super hero powers?  Indeed the powers had been spent.   I needed to expand my tribe so I began with the obvious.  I reduced my hours at the office.  I called upon our family doctors who helped me heal my sick family with medication.  Another gift they gave me was direction and strength to reach out to licensed therapists to mend my family's fractured hearts and souls.  

So many times I said..."I got this" or "Therapy is for the weak" or "Nothing is wrong".  I was clearly lying to myself.  Bringing in licensed therapists was one of the best things I have ever done for me and my family.  We are in a place of healing instead of an infectious, and destructive pain.  The lesson I learned is quite valuable and I should have called upon the licensed therapists sooner.   I know now "I did not have it" or "Therapy is good for all" or "Many things were wrong".

Self therapy has been an important tool also.  As a family we went to Build A Bear to put some positive energy into our hearts and souls. We chose a Dalmatian to represent our rebuild.  Dalmatians are intelligent, energetic, and most importantly loyal. Their spots are badges of great honor. Meet our rescue team...

Sgt. Scruffy Shelley

Dr. Tonto Shelley

Princess Shelley

Dream Shelley
The Rescue Pack


Much love,
Michelle D.  Voss-Shelley, APA

(Mom to seven year old Aislinn living with a GRIN1 mutation)


  

    


Monday, February 9, 2015

Aislinn’s Treasures-Making a living

Aislinn’s Treasures-Making a living

Life never seems to amaze me.  So far 2015 has been a filled with positive things.  Aislinn’s liver enzymes (ALT and AST) are back to normal after being several times higher than the norm.  Another surprising benefit is that her heart rate has been lowered and her oxygen saturation has been raised since removing Dilantin as her daily seizure medication.  Truth be told, Dilantin ended up being very hard on Aislinn’s little body. 

Too high! 
 

The culprit!  

Hooray PulseOx is in normal range!


Major adjustments had to be made to her seating system.    Adjustments included a new custom molded saddle and back support.  All parts were elongated to accommodate a large growing spurt.  All in a day’s work when caring for my beauty!

I am a big girl now!

We just rocked an Individual Education Plan.  It may have been the best one yet! 

The beginning of the year also brings an opportunity to thank the many kind souls who helped close out a very difficult year for Aislinn.  I am grateful that my blogs have reached Virginia, Pennsylvania, overseas to the UK, and Sweden!  Recently I learned that my blogs touched the hearts of the employees of Distribution Systems, Inc. (DSI).  Their philosophy is: “We are committed to helping businesses growth.”    

I am humbled the generosity of the business leaders of DSI such as Jim Stover, Tim McCain, Wally Peterson, and Bruce Fear.  These men gave to Miracles for Mito in honor of Aislinn.  How cool is that!?!  Seems to me DSI also helps non-profit organizations succeed!  Your gift helps families with items not covered by insurance such as an adaptive bike, a staircase chair, joint ventures for adaptive toys, assistance for a vehicle or its modifications, and much much more!
 

Life never ceases to amaze me.  I believe the following quote says it all.  “You make a living by what you make and a life by what you giving!” –Tim McCain.

Blessings to all reading my blogs and supporting organizations for children and adults in need!  

Much love, Michelle Voss-Shelley (Mom to eight year old Aislinn living with a diseased GRIN1 gene)









Monday, January 19, 2015

Aislinn's Treasures - The Oh Sh!t Bag

Being prepared is no stranger to me.  At the tender age of 13 after I accompanied a friend to work at a local bank, I knew the world of finance was the career for me.   It also helped that I was a math whiz and had an appreciation for money.  Back then I only had to plan and take care of myself.   Hmmm thankfully my family, career, and responsibilities have come a long way. 

Today, there are days I am lucky if shoes match my outfit and that there are no holes in my stockings.  I run out the door to join the rest of humanity on the highway in an effort to get to work on time.  Conversely, there are days when work has to be set aside because what's happening at home is a true emergency.

Recently, I had such a day...ok a week…where work had to be carefully placed on the back burner.  The day started out in its normal controlled chaos to get to work and get Aislinn’s sister off to school.  Aislinn had another plan.  She went into a deep seizure.  The first step in the seizure care plan was implemented and failed.  The backup plan was implemented and failed.  Panicked and concerned the final step in the plan was implemented...call 911. Tick tock...time was running out with the seizure at 10 minutes.  Tick tock....15 minutes passed as the seizure continued as the paramedics were wheeling away my baby on a gurney hooked up to oxygen..  Daddy was hopping into the back of the ambulance with his bag in hand to continue to fill in the EMTs.


Tick tock...no bag was pack for AISLINN!   Thank God for Aislinn's nurse who arrived minutes after the fire department and ambulance.  She helped center me to get the essential items packed for Aislinn.  After the ambulance left I still had to find a safe place for Aislinn’s big sister and pack more items so I could be on my away to chase the ambulance.  The ambulance was already ten minutes ahead of me with lights and sirens. I prayed and crying the whole way.  It seemed to be a lifetime before I saw Aislinn again at the Emergency Department at Children’s Hospital Colorado.

   
  


 

I learned a lot from that morning.  I learned my husband rocks in an emergency.  I learned the importance of having an emergency bag ready to grab and literally run out the door.  I now appreciate the importance of being able to lay out a plan for the fire department and ambulance. 

Humor is good medicine and the way I put together Aislinn's the emergency plan is no exception. There is now a calling tree to alert Aislinn’s hospitalist, and neurologists.   A designated bag was created for her.  It has a backup feeding pump, chargers, food, a list of supplements, a list of medications, and a schedule to administer medications, normal daily supplies (feeding bags, tube replacements, extensions, dressings, diapers, clothes, etcetera), and a list of supplements.  Most importantly,  I have a physician's letter directing treatment for seizures which can be implemented at any hospital or Children's Hospital!  The bag is red.  It stands at attention by the front door.  It is also clearly labeled the "Oh Sh!t Bag”. 



I share this piece of Aislinn's  journey in hopes that in an emergency you or your loved one have the basic essentials packed along with a physician's letter to direct treatment for seizures, a head injury, autism, diabetes, a heart condition and so on.  You might find a perky color, tag, or name for yours too.  Maybe it’s a Louie Viton or Coach bag because you've got swag!  It was no fun trying to think of what was needed in an instant.  It was no fun finding the right treatment or communicating past treatment when all I could think of is not being with my daughter or worse yet, not bringing her home.

Be over prepared.  Have a multiple level emergent plan which includes the best treatment for your condition.  Above all pack an "Oh Sh!t Bag" for you and your care giver.

Much love,
Michelle D.  Voss-Shelley

(Mom to eight year old Aislinn with a GRIN1 mutation)