A photo of me at home

A photo of me at home
A new photo of me and Jean at home

Tuesday, 22 October 2013

Life with MND - 2013 - September

September
 
On the 3rd, an engineer and Occupation Therapist both involved with Wheelchair Care made a ‘home visit’ and measured me up for a new chair to help posture.

On 4th with great reluctance, but further weakening of arms mean I am unable now to support my electric razor and I’ve had to ask morning care team to shave me. Shaving and cleaning teeth have always felt very personal to me, but one gone and feel cleaning teeth will not be far behind.

On the fifth, Jean had both big toe nails completely removed, because of ingrown nails. The mind shudders at the very thought of it! The removal went as planned, then it involves months of bathing in hot salt water and changing dressings, and on the Saturday she was at our timeshare in Aviemore for a week’s respite.

As a core tiredness creeps over the body the effort for typing procedures was lacking. Luckily I had the foresight of forward planning and had the procedures all printed out, just as well as I’d two new carers during the week, plus our Allison, our daughter, who did one night’s sleepover. With Ross, who lives locally tending my needs during the rest of the week, including sleepovers.

 On the 26th, L eon our great grandchild had his first birthday and I took a severe deterioration in my MND condition. Could it be life for one just beginning , whilst  another  was on the way out, I’d like to think so anyway!

To end the month, Jean phoned Doctor. On3oth and requested that I was ready for a P E G to be fitted (Percutaneous endoscopic gastrostomy) instead of taking in liquid and food through the mouth it’s a device fitted into the abdominal wall to get special food supplement into the system. This is in preparation when not able for any reason to take food or fluid in through the mouth.

This month’s notes may seem terse, but the effort and focus needed now to compose my notes creates a sense of urgency.

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