Sunday, September 10, 2006

I'm pleased to report that I successfully escaped from the hospital on Thursday and am now relaxing back at home. Andrew has taken a few days off work, and mum is coming to stay for a few days at the end of the week to help me out (and no doubt try to make me eat something every 2 minutes). The good news is that I've spoken to my transplant co-ordinator about my weight loss and at the moment I can remain on the list. However he did stress that should I be called in the near future and "arrived looking like a skeleton" they would be unlikely to proceed with the surgery, so I have to make every effort to improve the situation. He wants me to call next week with an updated weight...no pressure or anything.


I was particularly relieved to be home for the weekend, as yesterday was the 2nd anniversary of losing my sister to CF. She has been on the transplant list for 2 1/2 years, but sadly, time simply ran out. We had a family gathering at my parents house, which was a lovely way in which to remember her.

I must say that the expression 'time is a great healer' is, for the most part, true; in that the rawness of the wounds fade, the sharpness of the pain dulls and the memories become ones that more often make you smile than make you cry. Yet there is still not a day goes by that I do not miss her with all my heart. Those moments in the day where something happens to make me laugh or cry out loud, and for a second I think 'I must tell Frances Ann about that later', and then remember I can't. When I see something in a shop that I know she would have loved, and I have no one to buy it for. When I say or do something I think is hilarious, then realise the only other person who would agree is her. The awkward instant when you meet someone new and in polite small talk they ask if you have any brothers or sisters, and you don't know how to answer. To say "yes" no longer seems truthful, yet to say "no" is to deny her very existence.

In the most selfish way, I truly thought when my time came to be listed for transplant, she would be there to guide and support me through the journey, having already been there herself. Although she is not with me in a physical sense, I have come to realise over the past 2 years, that she will always remain with me..through my memories, my thoughts, and through the belief that I will see her again. When I write about window cleaners and motorised beds, I can hear her laugh; when I write about buying handbags and shoes, I sense her approval; when I write about this journey towards transplant, I know she is beside me. Every step of the way.

7 comments:

Tinypoppet said...

I dont really know what to say lovely...except that I wanted you to know I am reading and sending you an awful lot of higs and more. xx

Anonymous said...

Wow! It is good to know that your memories of Frances Ann more often make you laugh than cry. That's a tribute to the kind of person she was. For me, her laugh is what I remember most and how distinct it was. No matter how she felt emotionally or how ill she was physically there was always a laugh bubbling below the surface just waiting for an excuse to pop out. I learned so much from her in terms of dealing with personal struggles. She always helped me to put my own life in perspective. For that I will always be thankful. She was one of a kind.

B xx

Anonymous said...

You know I still think about your wee sister jac, and I really really feel for you; its uncanny the way they can be so alike us, even while they are so different. Its such a shame she isn't here gor you now, but she is still watching and listening and coaxing you on.

I'm glad you're bcak at home and could remember he with your family; best of luck with the weight gain, maybe Guinness is the way to go?!

Much love
Fi

Nicola said...

Hi Jac,your post was really touching.Although I don't know what it is like to lose a sister to CF,I do know what it is like to lose someone close to you,and even though you learn to smile instead of crying when you think of them,you still miss them.I couldn't imagine life without my twin brother.

Though I'm not on the Tx list,sometimes the thought of this waiting game fills me with fear.I guess all you can do is hope,and keep hoping.I really hope that you don't have to wait much longer before you get your call.

Nicola x.

Anonymous said...

Hey

Just wanted to post a wee message to say that you're a wee star and I'm sending you lots of hugs. Frances Ann was an amazing person and I often think about her. I've no doubt either that she is with you every step of the way.

Love ya millions, Claire xxx

CB said...

Fran, and indeed you and the whole family changed my life for the better in so many ways, and I'll be ever grateful for that. To this day, she has been the most well balanced, smartest, most understanding and just the most wonderful person I've ever had the pleasure to have met, let alone be so close to.

A beautiful post and such a lovely rememberance, Jac - keep smiling :)

C-x-x-x-x-

Anonymous said...

I have to say its god to read your comments about how much you miss Fran and what makes you think of her. Its just the same for me (especially when I'm shopping, I keep thinking I've forgotten something but its just that my shopping buddy isn't standing beside me saying 'you like that??! don't do it sarah!'
Remember when you have a 'I must tell Fran that' moment there are still people around you who can help you imagine just what her response would be and laugh along with you.
love you millions!
sarah xxxxxxxxx