This day last year, I received the call that has changed my life. If you have only recently started reading my blog you can read about the events of that day here.
As you can see above...Before that day, my life consisted of at least 9 hours a week being attached to a machine to keep me alive, massive painful needles inserted into my arm to allow my blood to be cleaned. I felt wiped out/faint after dialysis often having really low blood pressure and experiencing crippling cramps. I had to keep to a strict diet and fluid restriction, I was tired and nauseous all the time.
I didn't have much of a social life, and didn't see my friends that much outside of university. I couldn't go to the shops without a sit down every 10minutes, I had lots of time of university ill and basically wouldn't know how I would feel from one day to the next.
Now... I can't even explain the difference.
I have freedom from dialysis, Mondays, Wednesday and Friday nights aren't spent attached to a machine, I don't know how I had time to fit it in before... my time is now spent with my family an friends.
Instead of massive needles in my arms every other day I have blood tests with small needles once a month. My anti rejection drugs keep me alive instead of the dialysis machine. I never have cramps anymore and I never feel faint! I can eat what I want (within reason obviously) and I have no fluid restriction which is amazing... I can go out for a meal and not have to worry what to order or that I will only be allowed one small drink with my meal!
I have a social life, I have seen my friends more this year than probably the past 3 put together! I can just grab my keys and drive to my friends houses without the worry of feeling ill, I can be spontaneous which is an amazing feeling. I can go shopping all day and not have to sit down as much as I previously would... the only reason I will sit down now is because my feet are hurting not that I am worried I will fall down if I don't sit down. I can do more than one thing in one day... this sounds ridiculous but before if I knew I had to go to university one day I would I would not be able to do anything else that day as I knew I would be wiped out so I had to rest before I would do anything and then most likely sleep afterwards.
I don't have the worry of how I will feel from one day to the next... I feel great!
This was me 25th October 2008...
Today I will be thinking of my Donor and their family who gave me the amazing gift... the gift of life... I can't put into words how grateful I am... My life has totally changed and I hope I make them proud with what I am doing... I am thankful everyday.
I will share tomorrow some of the things I have achieved this year that wouldn't have been possible with out my transplant...
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5 comments:
Happy transplant anniversary Holly :D
Hugs,
Moll x x
yay!!
Just an excellent blog you have here. Its very information and I enjoy reading it. I try to visit your blog about twice a week just to see what you have posted :) Keep it up. I was wondering if you can exchange links with me, my blog is http://dialysis-patient-care.blogspot.com, it will really help our Google PageRank and at the same time, it will increase our visitors. I would love to share you stuff to my readers. I went ahead and added your blog to my blogroll, hope you can also do the same.
Sincerly,
Emma
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