This term has been hard.
There has been so much variety and I have seen an unacceptable level of poverty and privilege.
Here I am.
The holidays loom and I don't quite know what will keep me busy.
Keep my mind off it all.
This term has been hard.
There has been so much variety and I have seen an unacceptable level of poverty and privilege.
Here I am.
The holidays loom and I don't quite know what will keep me busy.
Keep my mind off it all.
I cried in the bath yesterday. I cried because I know I'm going to miss part of my daughter's life.
Tonight I cried because I felt like I'm going to miss more of it.
I have to realise I can't be there always.
Her dad will be fantastic
Her dad will hold her and love her
And he'll tell her when she needs telling
I'm so scared I'll miss it all
Being an ex pat is the most ridiculous thing to be.
We're immigrants.
We have the extraordinary experience of being here.
I'm not sure how we get to term it differently.
Humph
I want her near me every second of the day.
I want her safe in my arms, a place she can't stay
I want her to know my love is in her skin
To keep it there I must being to let go
I've been both this week.
News that a friend was suddenly dead and by suicide was hard to take.
I would love to be at the funeral as I know thev love that works pour out from everyone.
Her life had had so many difficulties, and some of them so close to my own experiences that she just got me.
We meet via a choir and when the choir spilt we went to different ones, but not once did that mean we didn't respect each other.
We became friends because she was open to me, open to learning about me and I her. That's what friends are I guess.
She knew what it felt like to have a body that fucks you over.
She knew what it felt like to be in hospital while you're children observe all that you're going through.
She knew the value of psychotherapy.
She knew what being betrayed felt like.
She also knew how to fight on. I can only guess that the fight became too much or that she was taken over by the pain and fear of depression.
I'm so sad she couldn't stay with us. I'm angry that she's gone because I don't want her to be. I want to hike up that bloody hill and see her next time I'm home. You take it for granted people will be there. And these moments remind you that won't always be true.
So I've been angry. The universe has pissed me off.
My mum and I would wonder when I would get my...fuck off to Disneyland moment.
Your cancer needed to be terminal.
But we never really know. And it will come back, without doubt. So we realised, we don't get to cash in and fuck off to the life long dream.
Mine is not and never has been Disneyland. But it seemed the most popular choice.
Today, as I watched the clouds over lake Malawi and let the wind cover me in a smooth coolness on the boat that took us from island to island, and as I looked at my new friends and beautiful little family, I realised, I've done it!
I've had my 'life is too short' escape.
Malawi is my Disneyland.
2019 will have some surgery in it but I'm determined not to let it spoil this escape.
Well, it is the rainy season.
Unlike the refreshing power of the rain here, VHL comes time and time again. You know it will show up. When? You can make a good guess and that is... Too often.
I'm trying to enjoy this moment and having the never ending support from those I love, and love me is helping.
The rain that is beating down around us tonight is, according to the locals, unusual for this time of day.
The reocurrance of kidney cancer is frustratingly normal and yet it beats down. Hard and unrelenting.
The simplicity of it.
The truth of it.
The way it does its job
Well done rain.
I applaud you.
Job well done... Keep it up.
Well, stop for a bit while I enjoy a bit of sun, tomorrow will do.
You've cooled and nourished us, me.
I do like the rain.
Two letters arrive at my old, old, old, old, old, old address.
They contradict the emails I've had.
They send me into the state of the unknown again and they make the evening frustrating and I feel sad and confused.
I'm now back in the doubt and so despite feeling I knew what the plan was, it's changed or has it?
And it's one of the good ones.
In the last month I've heard of two men who have prostate cancer.
Oh, one of the good ones
Kidney cancer isn't normally considered one of the good ones, but if I'm being positive, it is for me.
One day I might run out of kidney. I might run out of both.
But not yet.
I remember the phones on the wall. It was a day in March. A month, that until then held no significant to me and will now forever be, the month.
I was aware that I should tell people. I was old enough to have people of my own to tell. I don't recall how I paid, but I stood against the wall, in amongst the wall of phones and called someone.
I told the person on the other end. He's brain dead they think. He's dead they think.
And I recall being aware of the momentous event and my place in it. Small and sad.
Nothing more then.
I was surrounded by people who were leaning against that wall of phones. Some with good news, some bad, some mundane.
All with someone to tell.
Today I have a wall of people. I lean against them when I need to tell someone.
It will always be there.
This doesn't go away and never will. Stoic and able to comfort those who need it.
It's fine
I get tumours
Shut them down
No sympathy required
Those that know a bit more, read it... I don't want to dwell
I can't
I can't
I can't
And when I do - who wants to listen?
Very few
And I included myself
I don't want to listen
I don't want to
I don't what to chase
I don't want to ask
I don't want to know
I don't want to stop
I don't want to carry on
I don't want to cope
I don't want to fall apart
I don't want to
Some days I just can't believe what I'm juggling in my head. And there are people here who see and know that.
But not my husband.
When asked, do you think I'm impressive how I cope with all this, he replied
The doctors are.
But me?
I've blocked out the exact details but the gist was no.
No
No
And I didn't know what to do with that.
Did I show weakness by asking?
Is it that his permanent ex-pat lifestyle has left him devoid of understanding.
Or
Is he right
Nothing special about living with VHL.
The surgeon has a knife.
How far should it go?
How often can you be cut and how many times will it hurt?
Facebook tells you about memories. I'm struck by where I was three years ago. I'm in Zomba today and I climbed and walked and saw things I never imagined I would.
I did it with new friends and my little family.
I'm troubled by the next phase but not thrown by it.
I will make it through and I have such a huge amount of love and support.
Today I am aware of how blessed I am, despite my next VHL hurdle.
An account of my thoughts and feelings about having a genetic disease. Von Hippel Lindau disease, VHL. Not necessarily factual but real all the same.