Dealing with the Triple A’s

Anger – Anxiety – Abandonment.

My triple A’s.

I’ve been missing Hannah a lot this week.  Some of it is because the kids started back to school, and I keep going back to how so damn close we were getting Hannah into school.  Ethan and Abigail were so incredibly excited to have their little sister at the same school with them.  She was to start school the week after she first was admitted to the hospital back in September last year.

Instead, we brought her home three weeks later … knowing that her body was failing her … knowing that we couldn’t fight anymore for her … knowing that the deterioration of her brain from the Gaucher’s was causing her unbearable pain and irritability … knowing she was so unhappy and uncomfortable …

Knowing that she was going to die.

There is still a rawness that I feel when I think about her sometimes.  Not all the time, but sometimes.  The “sharp knife of a short life.”   It mostly happens when I am alone and find myself zoning off thinking about her.   It is just this overwhelming, crushing feeling in my chest.  I don’t even realize that I have tears on my face until they are rolling down my cheek.

My triple A’s.  I can’t say they are all brought on because of my grief.  Some are.  There are other forces at play here, other people and situations in my life.  That is where I am at now.

Angry, feeling abandoned, and sometimes not feeling like I have both feet firmly on the ground knowing what direction I am going.

Despite feeling this way, I’m very proud that I am doing this all my way.  My way with the complete love and support of my husband and kids.  I don’t care how other people think I should be handling my situation.  I don’t care how other people may not agree with the decisions I make for myself and my family right now.  There is some relief of stress when I came to the realization that the judgement of others on how I should grieve, “move on,” etc., should not and will not play any part in my grieving process.  I can’t change how other people think, and I don’t have the emotional energy to try to get them to understand what I am going through.

Doesn’t make those triple A’s go away though.

Unexpected Pangs of Jealousy

Unsure of Mickey at first ~ Who would have known that Mickey would become her favorite?

I came across this post written by a mom with a medically fragile child.  “Top Ten exciting things about having a kid with a rare disease.”

As I was reading her list, I started laughing and saying to myself “Yep!” to each one.  I could totally relate to each one as I have lived each one, multiple times in the past few years.

My heart sank.  I realize that is not my life anymore.  I don’t care of a medically fragile child anymore.  My two living children thankfully are healthy and seem to have the same issues as  other normal-developing children.

I got jealous.  JEALOUS!   Tears started, and I was getting angry at myself for being jealous.  Why the heck would I be jealous that today another mom is having these experiences?

Then it finally hit me.  I’m jealous because if I was having those experiences today that would mean Hannah would still be here.

I would go through hell and back if it meant that she was still here with me.

Jumping into the Big Pond

Next month, my husband and I are going to the first annual RARE Tribute to Champions of Hope Gala and the patient advocacy meeting they are hosting the next day.  This will be a place where patient communities, like our Little Miss Hannah Foundation, can engage with each other and experts on various topics ranging from legislation to non-profit business models.

At the 2012 Tribute Gala, we will honor individuals for their contributions in the areas of advocacy, science/research, industry, policy and global collaborations.

Please join us for a night of inspiration and hope as we recognize individuals and organizations that are working tirelessly to help millions of children and families impacted by over 7,000 different types of rare diseases.

As ANYONE who reads my blog knows, I am very, very passionate about create awareness for childhood rare diseases.   It isn’t something that I do for fun.  It is something that I HAVE to do.  It is so hard to explain because before Hannah I never felt very passionate about any cause.   But this has grabbed my heart completely.

Awareness for life-limiting children’s rare diseases, my focus…It is something that just has to be done.

Chris Mann

So next month, we are going to this conference to meet all of those people who have fought so hard for rare disease.   The “celebrities,” if you will, of rare disease awareness.  I have no idea what to expect at the “Gala” that night, but I am thrilled that we are able to go.

Best of all, I get to be a small part of that evening.  I was asked  to submit Hannah’s story for their “patient stories” section of the program.  To me, that was a huge honor!   All these people from around the country are going to read about me and my daughter – me, just a “Mom on a Mission” living in Vegas.

Besides, seeing Chris Mann (from “The Voice”) performing that night at the event is NOT a bad thing either!

Bring on the pain

Hannah may not have been able to eat the candy, but that did not stop her from eating the wrapper with the candy inside! Oct 2010

The kids go back to school in 11  days.    This was such a crazy summer, and it was very much our most frugal one ever.  But we are almost there.   We did have some great times like visiting with friends in Northern California and Reno plus lots of shows on fillaseat.com as well as taking in some fun community activities.  The kids are completely tan thanks to all the swimming at my inlaws house and other friends houses.  Abby and I did quite a bit of mommy-school to help get her prepared for third grade.   And we can’t forget our LMHF inaugural event which was, by far, the biggest thing we did this summer.

So much different than last summer.

This time last summer, we were still fighting for Hannah.  Driving to Los Angeles  to meet one of the top movement disorder specialists in the country.   Never would have thought a few months after that visit, Hannah would be gone.

For me, the nights still suck, the meds I am taking still take a few hours to kick in.    But it is almost like a willful punishment because I want so much to remember Hannah, trying to remember the little things that are slowly disappearing from my memory, wanting to relive the times that she was here ~ remembering what it was like to feel whole again.

Her death has left such a massive hole in my heart, my life.   But I would rather feel the pain and get to be with her, even in memories, than not think about her at all.   That old saying – better to have loved and lost than never to have loved at all…so true.

The love I have for Hannah is … there are no words.

 

Our Rainbows to the Sky Event

event 34(click for event program)

On July 25, 2012, the Little Miss Hannah Foundation launched ourselves into the Las Vegas community with our “Rainbows to the Sky” event, our first fundraiser and community event.

DJ Miguel Guidos of Soli Concepts Entertainment kept the crowd going with great music, audience participation, raffles, and the highlight of the evening…three balloon releases sending up over 400 balloons.   Each of these releases sent balloons with personal messages written on them up to heaven.   They were all incredibly moving, especially the 7:30 pm special children’s release…

(click for more details, pictures, and videos)

Happy Birthday Hannah

Happy birthday, Hannah. I miss your smile, your wiggle, and that adorable little laugh of yours. Most of all, I miss your snuggles, cuddles, and just having you are my arms. Not having you hear with me hurts my heart, my soul. Daddy, Ethan, Abigail, and I miss you so much. ♥