Sunday, November 13, 2011

The waiting game


Well testing is done and the last two days have been spent just hugging and cuddling with Cora. The testing on Friday went as planned and Cora endured it like the trooper she has been all along. She started the fasting at 6am and we were in x ray by 9am. I dreaded the pig-o-stat more than she did. Cora was strapped into it with her arms in the air, the plastic strap under her chin and her legs hanging, and smiled the whole time. I am continually amazed and awed by the open love and happiness this daughter shows to those around her. Once that was done she was given the sedation for the echo-cardiogram and the EKG. This time the sedation hit her pretty hard. I don't know if it because she is weaker now than she has been in the past, but she was groggy and floppy all day long. After that testing was done one of the Cardiologist from the team that will be operating on her came and talked with me about what to expect.

The whole team is pretty optimistic about Dr. Bove being able to do the repair. Although they did again talk to me about the artificial valve being a possibility. I am praying this is not the choice that is presented to Dr. Bove when he does the surgery, for if he has to do a mechanical valve that means several operations in the future for Cora. During the Echo they found the valve had prolapsed and there was a cleft of some kind. That's all I could gather from the discussion and really that's all I wanted to hear.

I again say that if Cora has to be anywhere I am very glad it is here at this hospital. The University of Michigan Medical Center is one of the largest concentrations of medical education, research and treatment facilities in the world. Located on 82 acres this 30 building complex includes a premier medical school and world-renowned, advanced patient care facilities. The Med-Inn is located within the walls of the facility and makes it very easy to see Cora and be within pager reach if I am needed.

Tomorrow fast approaches and I find the anxiety grows as the hours of today slip away. I watch Cora sleep and I silently pray for the patience, the understanding and the faith that I will need in the early morning hours tomorrow. Just like Cora, I truly need to take one moment at a time tomorrow morning and have faith that whatever happens it is for Cora's greater purpose and not necessarily for my understanding.


Friday, November 11, 2011

We've arrived

November 10, 2011
The six hour drive to Ann Arbor was made during alternating sunshine, snow, rain, sleet, hail and high winds.  We arrived safe and in time to check in for our reserved room.  Cora was so happy to be out of that car seat and able to roll around on the bed and stretch her legs.  She settled right in and was ready for tickling and playing.  My three travel companions, my daughter Emily (17), Cora and my mom, were a little giddy after the road trip, so they were more than happy to play  while I unpacked Cora's playpen and toys.
 < three silly travelers
 < the almost serious 'we've arrived' photo

It is a relief and a sad reality that I knew where to park, where to go, the shortcuts and the how to's of the way things work and what I needed to do for Cora's workup tomorrow morning. It was definitely a mixed feeling of joy that I and Cora were recognized by many of the people here and a feeling of sadness that we were recognized.  Cora was greeted with a great deal of smiles and the kind of well wishes that usually started with , "Oh, Cora.  You're back.  You look so happy but I wish we didn't have to see you again."  A greeting that I totally agreed with.

< room view


So, despite the fact that we are here again for another major surgery for Cora Jean, I wouldn't pick another place to be with her.  There is a sense of relief for me because I know that if Cora has another sudden medical crisis I am in the perfect place for it to happen.  At home there is always the worry that she will take a bad turn and I will again have to rush her here.  Strange how I recognize a sense of relief during a stressful time. 

So it seems only natural that I end today's blog with another milestone for Cora that takes place in the Children's hospital that she has spent so much of her first seven months of life in.....She was able to hold her bottle by herself for a feeding.(first time for her to accomplish this)  Go Cora Jean, Go Cora Jean, yeah Cora Jean!


Wednesday, November 9, 2011

Unexpected Gifts

Whenever I sit here typing this blog I see the little stack of the medical bills that need to be paid.  I have been so worried about these bills that are starting to come in , as well as other normal household bills, that I haven't been sleeping very well. I am definately concerned with getting enough funds together to take Cora to Ann Arbor again while still meeting my other obligations. It has gotten to the point where I sing Cora to sleep and in the song I make up silly words about the angels coming and paying our bills.  Then this happened:

One of the local Down syndrome associations found out about Cora's upcoming surgery.  This is the group that helped me so much before Cora was born and sent me tons of information about Down syndrome.  After forwarding the information for Cora's blog, I received an email from them and they informed me that they were sending a monetary gift to help during the upcoming surgery. 

It was such a tremendous relief to hear this news.  Anyone who is a single parent knows the struggle that we face on a daily basis to support our children in the ways they need it.  Emotionally, spiritually, financially, etc. Let me just clarify that being a single parent with Cora is not a burden for I enjoy her presence and the other kids enjoy their sister.  Yet, it is a tremendous financial strain becuase of all of Cora's medical needs.  I am not one to tell people about the stress I am facing or the financial burden I am under because I just feel like it is my responsibility and not anyone elses, and truthfully noone wants to hear about that.

Then I receive the email that this group was sending me a monetary gift to help with Cora's surgery and my stay during that time at Ann Arbor.  To receive this gift, so freely given, brought tears to my eyes. A gift given with understanding and nothing expected in return. A kind of gift that touches the heart as much as it eases the financial strain.  A coincidence?  Nope, I believe it was divine intervention.



Tuesday, November 8, 2011

The first secret

I watch Cora playing in her playpen and I am amazed at how far she has come.  I see the NG tube in her nose and watch her try to pull it out again, despite the fact that I have been taught by her how I need to tape it to keep her from doing this. I see her grab different toys and rattle them and try to get them to her mouth.  I watch and listen as she talks her baby garble words and see how successful she has become at moving her tongue to make different sounds.

To Cora, life is an opportunity.  She doesn't care that she has to nap every few minutes because she has so little energy.  She doesn't mind that her heart isn't beating or working like it is suppose too. She has the trust that when she reaches her hand alongside her body that hand will find a toy to play with.  She knows where I am and searches for me.  When she finds me she smiles and laughs, because she knew I would be there.

I watch her and I am reminded of that line by the writer Robert Frost were he says, "I always entertain great hopes".  Cora is like this in so many ways.  People are always commenting on how   quiet and happy she seems.  I agree.  Cora has the ability to be so peaceful, and many times lately when I hold her in my arms and cry at the injustice of our life and events right now, she will look at me as if she carries the wisdom of centuries and hold my gaze.  Those little blue eyes seem to be telling me so much and, despite this sounding strange to some, as she holds my stare and gazes into my eyes, I would swear I can hear her speaking to my soul. 

This little child is such a blessing.  She has a mind that is open to everything and attached to nothing.  She knows the first secret in wisdom, without having to be taught what that is. What an absolute gift in today's world. 




Sunday, November 6, 2011

Like a willow tree

I have learned during this experience with Cora that I have become a willow tree.  Not another kind of tree, for an Oak tree is very strong, but it is not flexible.  If a strong wind comes up the Oak tree fights against it. If a terrible storm comes upon it with a great amount of wind, the Oak tree will likely break instead of bend. 

Me, I am like a willow tree.  I am like Cora.  She just goes with the flow.  She smiles even when she is at her sickest.  She wiggles and flexes even when the nurses or doctors are having to cause her pain to make her better.  She cries against the injustice of it, and when the test or the medicine is over, she smiles and wiggles her toes.  Cora is happy to be here and is present in the moment.  Cora adjusts to the situation and bends freely.

Cora is teaching me how to be that willow tree.  That no matter what comes next, no matter what the weather is like on any given day of our journey, I must be that willow tree that bends and sways and curves and moves with the flow of the storm.  If I am like an Oak tree it is likely that I could break under the pressure of the storm or the suddenness of a turn of events on our journey.  Yet, if I am and if I become a willow tree, I will weather the storm, I will bend and flex with the next treatment or surgery that Cora needs, and I will survive the storm.  Maybe without a few leaves, but intact and smiling.

For I have learned a great lesson from my daughter.  If I am flexible I will bend with changes that might come our way.  If I am not flexible, I will break.  So, yes, I am a willow tree.....just like Cora Jean.

Wednesday, November 2, 2011

Throw out the bath water...not the baby

My grandma used to say this.  I remember her saying this when all the grown-ups would be gathered around the table for holiday dinners or for Sunday lunch.  Someone would be talking about a problem and this was a gentle reminder to get that person looking differently at the problem without letting it consume one's life.

I thought of this today when I was driving home from another appointment with Cora.  We had been to Marquette yesterday and today we drove to St. Ignace.  Both for doctor appointments that are centered around keeping Cora at her best with the way her heart is working right now. She hasn't grown any in the last month and she hasn't gained any weight.  The good thing about this is that she hasn't lost any weight either.  Cora has a little fat roll by her arms and Doc Statler called this her fat reserve.  Both Doc's were optimistic with the upcoming surgery. 

I, on the other hand, am fearful and anxious about Cora's health and her ability to tolerate another completely invasive surgery such a short time after her first one.

So, on the way home this afternoon, my mind was wandering to the "what if" side of things.  Never a great place to let the mind wander.  Then it wandered into the "don't know if I can do this" thoughts.  Then it wandered into the "there is no extra funds anywhere" kind of thinking. At one point it was dwelling on "am I giving all the kids the time they need".  Then my mind started doing the whole snowball effect, where one negative thought was leading to another, and another, and another......

At that point I very clearly heard my GranGran's voice say, "Katrina, don't throw the baby out with the bathwater.  Take one day at a time."  Good advice for me during this stressful time.  I looked out of the windshield of my Yukon and said a quick thank you to the heaven's.  I am sure GranGran was up there smiling at me and Cora.

 Cora after a bath-exploring the quilt pattern on my bed

Cora showing off her spikey after bath hair

First Halloween

Well Cora endured being dressed in a duck costume with beauty and grace.  I took her trick or treating with my son Phoenix, daughters Kelsey and Melissa.  Poor Emily was sick so she could not join in the fun. 

I wrapped Cora up in her blanket and put her in the stroller and we followed along with the older kids and toured the great town of Pickford.  Everywhere we went Cora was greeted with smiles and well wishes.  It was an amazing night and Cora was the cutest button around.

For Cora's  first Halloween it was a blessing and a treat to share it with all my children.  It was an honor to watch the other kids interact with Cora and see their pride in their little baby sister.  Not a single moment did I see them shy away from other friends  or try to hide the fact that Cora was their little sister.  I must be doing something right in raising this family.  I am so blessed to see the way Cora is teaching her older siblings to be even more accepting and open minded.


Cora in her duck costume (Emily is under the table with her hands behind Cora to help support Cora so she can sit for this cute photo)


Cora after doing a raspberry


Behind the scene helpers for Cora's "photo op"...(Melissa in Spartan hat, Emily in Blue shirt)

 Cora after her first Halloween.