IT has been one full year since our Rye guy passed
away. We have no more answers now than
we did then and we are still struggling to make sense of the universe and why
it would choose us and ours.
This grief comes in waves – I had been told that it would –
sometimes for no apparent reason at all it washes over you. Sometimes it is soft and gentle like the surf
lapping at your beach chair, but sometimes it just beats you into the surf and
tears your swimsuit off leaving you crying and naked and wet with your breath
stuck in your chest and the pain in your heart worse than ever.
Some days I get through the day one minute at a time. Sometimes it is one hour at a time. Sometimes I don’t make it through the day and
I sit on the couch or on the bed and I stare at the door or the ceiling or the
television that I am not actually watching. Sometimes I watch too much television.
It helps to stay busy, and I do that well, but sometimes I
just run out of energy and it is all I can do to get up and go to the bathroom
without melting into a heap on the floor.
My “good thing” at a work meeting the other day was that I
got out of bed and came to work. I would
have worn my pajama pants except that they didn’t have pockets and I have to
have pockets during the day. It’s a personal
rule. Im sure my co-workers were glad
that I have that rule!
Life goes on and so do we, my family and all the people in
it are changed now though. Every two
steps forward and then it seems something will happen and we go back to square
one. Sometimes it is only a step back,
but sometimes it feels like starting over.
The death of another person whether we know them or not sparks all sorts
of panic and setbacks. News that another
mother met the child that got her childs heart, or eyes, or lungs begins the
pain anew. She gets to hear her childs
heart beat again, to look into his eyes or to hear him breathe. I am happy for her and terribly jealous and
sad at the same time.
My hope and my heart keep thinking that once we get through
this horrible first year, that everything will start to feel better or at least
not hurt so much, so often. My head
knows that it won’t help to just get through this year, the next year will just
begin.
There is also the ongoing issue of “Does what I do
matter?” Every day when we get up we
have to find a reason to get out of bed, and then we have to convince ourselves
that what we do matters, and that if we keep going we will keep finding reasons
to go on. Some days we cannot find that
reason to get out of bed or if we do we cant focus on anything enough to
actually get anything done. Some days we
cannot find anything that matters enough to focus on. It just doesn’t matter.
Then there is the insomnia.
A desperate need and desire to sleep but a complete inability to do so,
we have tried everything, melatonin, Simply Sleep, working until we can’t move
anymore, to no avail. Alcohol does not
help. Nothing helps – so I get up and
get some things done – or I try to get some things done. Between the grief fog, lack of sleep and the
thoughts of my son it all gets jumbled into a tattered mess that cannot be sorted
out and does not allow me to focus for more than 10 minutes at a time.
Some have asked me to help them understand what it is that I
go through each day since my son passed but I cannot and I will not, for to
make them understand I will have to make them endure death by 1000 cuts, only
you don’t die you wake each day and start again fresh and raw and with that piece
of your soul missing. You cannot explain
how it feels. It feels like you are
digging a ditch on a beach with your forehead through sand that the waves fill
in as soon as you pass through it. You
feel like you should be able to lift your head and see all the beauty around
you on that beach which would be so lovely.
But all you can do is push sand with your forehead. Foggy and hurting and unwilling to have
anyone else feel that way.
I do not want to be touched or hugged even though I know you
need to do that – I feel fragile and breakable and I don’t like that feeling –
the more you hug me the worse it gets as though I am made of glass.
Some days even talking out loud hurts. Of course, those are milestone days when
18,000 people want to check on us – and we do appreciate that and we know that
you love us and that feels good to have that support and feel that love. We just don’t want to or can’t talk that day
or that moment.
Loud noises are not ok and neither are crowds of people
pressing and asking and wondering with all the questions in their eyes. Even though at one time I was the loud one! They wonder if we are ok and we have to say
yes – no matter what we are feeling because to not say we are would be to hurt
the person asking and then they try to “fix” something that cannot be fixed.
I once told a friend that in order to fix what was broken we
would have to have our son back. She
said “well then it would be the Zombie Apocolypse – and who wants that for
their kid!” I had not thought of Zombie
Ill be honest – just raise up him the way that other guys son got raised and he
was fine for years after that – you know who Im talking about.
I looked into the
mirror yesterday (something I rarely do), the one year anniversary of his
memorial and realized that he had my exact eyes. When I look in the mirror I see my sons eyes
staring me back.
Apparently all loss mothers feel this way – at least all of
the ones I have talked to do. They say
it never goes away. 17 years, 22 years, there
will always be some part of you pushing sand.
We will survive – the same way that other families have
survived this, from day to day and year to year. Yoga and meditation will help and maybe some therapy
too. We will find joy again in some of
the things that we did before and find ways to find it in new things that we
do. We will love and smother our other
child until he wants to scream at us to stop treating him like a baby – “I’m
gwown”! We will laugh when he acts just
like his big brother did and we will not let him get away with some of the
things that his brother did! We will
travel places and say “Rye would have loved this” and eventually we will go
back to the Highland Games and to the Fair again and it will be fun for us –
not something we are getting over with so that we can get that first time out
of the way on our own terms.
We should get to do just “whatever the F*&K we want to
do” – I was told that at the beginning of this journey, but life doesn’t work
that way. When one of us is doing good
it seems the other is not doing so good.
All of us doing good on the same day is a very rare occurrence and it
seems that we never get to be together on those days for long – running in
different directions taking care of the things that need taken care of while we
are up to it!
So if you should see us and ask how we are doing – let “fine”
or “ok” be the answer. That is the best
we can do without letting some of our hurt come out like the vicious demon that
it is and get all over you and yours.
Let it be. Blessed Be as we start
on the second year of the journey.
Dear Lisa,
ReplyDeleteI read this when you first published it back in September. I wept then. I weep again. This is incredibly strong. I just want you to know that. I read this and thought, "Lisa has a strength that could move mountains." I see you. I hear you. I feel you. Thank you for sharing in such a transparent way. Thinking of you all the way over here in the Butte. -Margaret
Thank you Margaret! I feel the love!
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