Family Wedding, PEG Op..

Just after diagnosis in 2014 I bought this board which was a little easier to paddle

Just after diagnosis in 2014 I bought this board which was a little easier to paddle

This month marks 3 years since my diagnosis & with MND symptoms 12 months prior I'm into my 5th year with this horrible disease & fighting it the best I can. Margaret Doody House is a MSWA Respite facility in City Beach that I stayed at the weekend before my daughter's wedding. I thought whilst my son was in Adelaide at the bucks night I'd get an idea what it would be like to be in a care facility. Not the best experience to be honest with other residents being mostly bed ridden. Anyway it was ok for a few nights but not long term, it's not for me at the moment but is probably inevitable I'll end up in a similar facility.

It's been a big lead up to Michelle's wedding & it didn't disappoint one bit. She looked beautiful for the big day & the venue was amazing! I couldn't fault the staff at Mandoon Estate they were terrific in organising the ceremony setup & keeping our glasses full at the reception. Such a wonderful day for Michelle, David & my family.

To other news with me.. I had a follow up meeting with my Neurologist regarding my PEG operation & it will be done within the next couple of weeks. I'll be in hospital for 4 to 5 days & family will be shown how to use & manage feeding me. This will be yet another part of my independence gone but it's required for my survival so I really don't have a choice. Extra care will also be needed once I return home & I'm just in the process of arranging that now. Apart from that I've been enjoying this sun through the start of winter, so much warmer than last year.

out and about.. the boys from Kisstake

out and about.. the boys from Kisstake