Week 411 “Back Home”

Finally I am back home with Jessie ( Cat)  I have certainly had a great time travelling through Queensland and NSW over the past 8 weeks. Jill would have loved the caravan park at Agnes Water. She certainly would have enjoyed the coffee at 1770 “The Tree” where Jill’s sister , husband and friends celebrated her birthday while our family and friends celebrated at home.

While at Cabulture an outer norther suburb of Brisbane I was able to visit Gay and her husband – Gay was diagnosed with MSA  in 2012. When I spoke to her her strength was evident and the care shown by her husband  was amazing. They are planing their lives with a cruise around  NewZealand in the near future.

I finally left the others heading for an overnight stop at Millmerran Show grounds – only a couple of van there but a real friendly care taker and a cheap stay $20  then across the Queensland/NSW border at  Goondiwindi to Narrabri – arrived early so had a walk around and some shopping – hot 35C. Early rise and then moved south to Mendoran – Free camp site that I shared with 16 others – I went too the pub for a beer and an evening meal. Next stop Forbes where I had an evening meal with other campers in the camp kitchen. Another early rise and I was getting anxious to get home but decided to stop at Narrandera . The last time  2011 Jill and I were returning from Hervey Bay we stayed there and I was able to get the same site. By evening the drive through sites were full. Next morning I only had about 3 hours to get home. I backed up the drive with the aid of my neighbours and was meet at the door by Jessie.

I have now been home a week – a couple of visits to Jill with some flowers, evening meal with my great neighbours – who Jessie thinks more of than me. A feed of whiting from Agnes Water with Pat and Keith and yesterday Michael & Amanda arrived for a few days.

I was contacted by a woman from Corowa who is suffering similar symptoms to Jill although she has not been diagnosed with MSA . She was amazed that we were so close.

I feel it is something I can do – talk to other MSA carers or patients and give some of our experiences. I noticed that the next MSA conference is in Washington DC – USA in October 2014 and my thought currently is to be there.

See you on the net

 

 

 

 

This entry was posted in 9. Exercise is our continued endevour. Bookmark the permalink.

Leave a Reply

Your email address will not be published. Required fields are marked *

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>