Effervesce.

When life knocks you down, calmly get back up, smile, and say. "You hit like a bitch."

Its been a while, but trust me, A LOT has happened!

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Ok, so I’ve been absent from my blog for 2 years. In my defence, my world kinda came crashing down. Several times. I thought 2009 was a rough year, sorry to hash this all up Sis, but its where my story starts, I have to start at the beginning, OCD and all that, you understand!

So in 2009 in April the 4th to be exact, my Sister who was pregnant at the time, went for a routine scan and the Dr found her little girl had died. Its hard for me to write this and not get emotional and teary, it still hurts.  Our world came crashing down. I had to watch my Sister suffer. Again. For the 4th time. And also the final time.  Her recovery from that was hard, very hard, nobody, and I mean nobody knew exactly how hard it was for her. I did, I heard, I knew. And off course her sweet sweet loving and ever supportive husband. I could do nothing. I felt and was helpless. All I could do was stand by and watch. No words.

But my Sister recovered. She grew into this amazingly strong and grounded person. I stood in awe as I saw her emerge from this painful horror story. She taught me so much. She is a happy well rounded person who isnt looking for that one thing to make her happy. And that, is amazing.

I didnt know how much I learnt from her and how much I would use these lessons until a year later. I was feeling ill, very ill, nausea stomach ache, tired, very very tired. I went to my GP, she diagnosed Collitis. Inflammation of the colon. She prescribed a heavy dose of antibiotics. I got worse. I went back and she gave me another dose of anti biotics. I got worse. At that time my husband told me to make an appointment with my Nephrologist. Now this is after my Sister had been on at me to go see him too, always asking me if it was not my kidney. I always said “Nah man! Dont worry, its not that!” Can you say DENIAL?

I went to see him, after I did the regular UK and E tests with 24 hour protein and createnine clearance tests. He took my blood pressure which was very high, a sure sign something is up. He took one look at my createnine clearance and said “Amanda your createnine levels are at 1400.” Which means renal failure. My kidney function was all of 4%. I really thought he was joking! He always jokes around with me! But apart from nausea only in the evenings I felt fine! So my world came crashing down once more!

We decided to go on holiday as a family. I wanted to have normal before I started dialysis, just one more time. It was a great holiday, but also a bad one for so many reasons. I also got really ill after that holiday. When I started dialysis my createnine levels were at 2700. The Dr could actually not believe I was still alive! And my heamoglobin was 4. He told my husband that not many people would be alive with heamoglobin that low. So I know ‘Im stronger than I think.

I started heamo dialysis in July 2011. I had a permcath (permanent catheter) in my chest, and a ripening fistula in my left arm. I used my permcath for 9 months, because I absolutely refused to use my fistula after I saw what happened to people’s arms after a while. Its awful, its hideous and very painful in the beginning. So amid a furore of nurses and drs telling me I HAVE to use the fistula, I said, “Nope” and stuck to my guns for 9 months. I am now doing peritoneal dyalisis. And I far prefer it to HD. My Sister was with me when I had the PD op done. I think she is still traumatised and probably in need of therapy which I will pay for! (chuckles silently) What and AWFUL op! I shall leave it there.

For 7 month my Sister and I did tests to see if she could be my donor. And she was! She is in perfect health and a great genetic match. We got our transplant date for the 30th of March 2012. We were extatatic! My Sister doesnt have children and she thought her destiny in life was to be my donor. At first I didnt want to hear her, but as the tests became clearer and we went further I saw that maybe she was right. And then, 6 weeks before our transplant surgery, my Dr pulled the plug. My world came crashing down again. My Sister and I were devestated. My Husband and my 2 sweet boys were devestated! Everyone we knew were devestated. My best friend heard through my sobs of the devestating news.  My Mom was devestated. It was awful.

But let me tell you, all these devestated people carried me through this. That was wonderful. Nobody gave me stupid platitudes, nobody said stupid things like “Its for the best” they just carried me through it.  And still are. I am truly blessed by the number of people who are just there for me. I gained a lot after I lost it all.

Not so long ago I told Pete I don’t want to be a slave to renal failure. I cant just wait for some random person to die to provide me with a life. And I hate being on the national donor list. But here I am. Because of the nature of the disease I was diagnosed with, a live donor is not feasable. But neither is a deceased donor. So my Sister, being the amazing person she is. Digs. And she dug until she found something. I’m seeing a Dr in October this year and I will say more about it when the time comes, suffice to say it looks hopeful, more hopeful than it ever looked. Im so excited for this appointment and really cant believe I have to wait so long, but I have no choice.

In the meantime, I will dialyse with my APD machine, and bide my time until then.

I have recently started drinking wine again, and I developed a taste for Bacardi Breezer Pineapple flavour, and I’m enjoying my life again. My boys are now teenagers and that keeps me on my toes!

You gain strength, courage and confidence by every experience by which you really stop and look fear in the face. You are able to say to yourself,  “I have lived through this horror. I can take the next thing that comes along.” You must do the thing you think you cannot do.

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11 thoughts on “Its been a while, but trust me, A LOT has happened!

  1. Awesome post sussie!!!!! You have handled your situation with such poise and grace! I love you and hope the next treatment will be successful. We will always be there for you, you are in our prayers always.. xxx

  2. It has been an honour & a privildge to walk with Elize on her journey of healing & self discovery! The love u have for each other is inspiring!
    All the best for the road ahead! Praying that the new treatment is a success!

  3. Looking back like this, I can’t believe the things we go through in our lives. In the middle of it all you sometimes can’t see the light, hope or future but yet here we are. I think we are more often than not, stronger than we think we are. The amazing thing about Amanda and Elize is that they keep on caring and giving and supporting others while they, themselves struggle trough adversity. The two of you inspire us.

  4. Pingback: #Dialysis and a Not Normal Day | DevonTexas

  5. Thanks for sharing your experience. I really appreciate how you “fell” into this and I’m sorry you have to join this particular club (kidney failure) but it’s not as bad as the alternative! LOL When you have a moment, please visit my blog about life on dialysis. I try to share and educate as much as Ican so others do have to learn on their own. http://www.DevonTexas.WordPress.com.

    Devon

    • Thank you for commenting on my blog! I will definitely go and check out your blog! And yes, it is better than the alternative.

  6. I had to return to read this again. Your experience , as difficult to imagine, is an inspiration. And with two young ones, too! My two boys were much older and perhaps that made it easier on them. They are now 20 and 21 so they were 17and 18 when I started dialysis. Anyway, just dropped by to say hey.

    • You know my boys did take the news very hard, but they are so supportive and very helpful now. I think it doesn’t matter how old our kids are they still worry!

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