I made a pledge with a close friend to climb Mt. Everest a while ago, I have always wanted to climb Everest. I know how much preparation is involved, all the climbing equipment, stamina and training etc. Also gain experience from climbs like Kilimanjaro, some peaks in New Zealand and South America too.
An Aunt said to me that this is my own Mt. Everest. The more I think about it the more it's true. I new what hardship was before this affliction, this has put a new meaning to the word 'difficult'. It has been difficult to breaking point in every aspect.
In fact there have been times when I thought freezing your bits off on a mountain was not so bad compared to this.
On the eve of treatment I am a mix of emotions like anxious, tired, scared, apprehensive, confused, etc.
Because there is so little known about this illness I have had to come to terms with the fact that nothing may happen when I undergo treatment.
But that is so hard.
My two children are so exited at the prospect of me being well again. Their outlook has been so good and positive. Which is helpful to say the least.
I had to explain to them that it might not be successful. (children see with such uncorrupted simplicity, if only things were that easy).
Meanwhile all I can do is think about what I will do if the treatment is a success.
7 comments:
Hey Phil, Mike here (Robbies Brother) Heard about what happened, tough going mate! So happy to hear you have finally been diagnosed and starting your treatment (Fingers crossed) I hope knowing what it is has brought you some sense of relief. Would love to catch up with you, maybe I can come and visit with Robby next time.
Keep well Champ
Mike
All the best with the treatment tomorrow. Hope it's fast, painless and effective.
Mate
Not sure if you will get this before the treatment, but I hope you do.
Hope that it all goes well and that it is outraeously successful. Will be cheering for you from afar. Imagine how strong the sun and clean the air will be when you get to the top of Everest!
Hi Phil
all the best and all bits crossed from the Nice 'Cabin Boy' Fan Club
we missed you on the last birthday trip.
the sun is shining here for you
bises
Karen
Hey Phil
Got your blog address from Stuart - and I have been reading up on your story about the illness and how it has affected you. Terrible and scary to think about how your life can be turned upside down like this - and scary to think about that it can take this long to diagnose an illness. But it also inspiring to read about how you seem to have handled it all. I hope that the treatment will go well, and that your recovery will be speedy. I will follow your progress via your blog and Stuart.
All the best from a cold and wet Denmark.
/Thomas Iversen
Hi Cuz, It's Michelle here. I know we haven't seen each other since we were kids but you have been in my thoughts heaps. Mum (Linda) has filled us in about your battle. We have been shocked to here about all the symptoms and how they have affected your every day life. I can't believe it took so long to diagnose. I truly wish you all the best with the treatment. Thinking of you and your kids heaps. xxx
Hi Phil
Leigh and I are thinking of you and sending love n good thoughts for today and tomorrow, as you begin to climb your Everest.
I think you need a pirate's hat to wear next time you go shopping...
love n lentils,
Jan
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