Ai, it has been a little while since I updated this blog. I obviously arrived home safely from Vietnam and made my way back to Tasmania. Then I got the call to confirm my availability for project in PNG, it was definitely on and I should get my act together!
With Cystic Fibrosis getting out of routine is always fraught with danger, I just survived Vietnam. So I beefed up my exercise, made sure I rode a little more, walked a little more and got myself in good shape to go help my mate Andrew in PNG. He is aware of my health, I stay with him, and he promises to look after me and take me to the gym regularly.
I am there now, to help out for three weeks. Three weeks I deem max without fresh air and good aerobic exercise. And I am just now entering my third and last week here. I ran with the Hash House Harriers a few times (life saver!) as they happily run (safety in numbers and good local knowledge). But I am starting to struggle now. Taking three different antibiotics and a barrage of other stuff, and I think I will be fine. Of course if it comes to the crunch I'll be on the first plane out.
Whilst here I am reading my second book on the El Camino de Santiago de Compostella, my next adventure.
EL CAMINO DE SANTIAGO
And why would a good Jewish born person like me attempt an 800+ kilometer walk with backpack? I will do it to bring attention to Cystic Fibrosis and Organ Donation and provide inspiration to people with disabilities. Of course I also think it would be fun, and might even be the source of another book or documentary - like www.coughingthedistance.com.
Slowly I am starting to work on logistics, taking names of interested people to join me, looking for sponsors who might like to donate money or goods. If you have a good reason to be involved, like to walk or support for 2-6 weeks in September/October 2012 do let me know (email@example.com). Although I will carry my own gear, we may have a support vehicle with us. The vehicle may not be seen for days at a time, but will carry team members that need a break (that won't be me!!) and do some sightseeing. Of course it is also important to have a vehicle for emergency backup as I do have Cystic Fibrosis and tides can always change - besides I am on the wrong side of the life-expactancy bell-curve). Things can always turn ugly, but really it also means people who want to come but not necessarily walk the whole way have the option to come along.