NHS

It’s been an interesting couple of weeks dealing with the NHS. I strongly support the idea of a health system for the people. The NHS tries to fulfil his roll but is underfunded ripped off by suppliers, doctors, and surgeons. GP’s on 100k plus are now nearly all going part time. The result, surgeries are finding ways to prevent people getting appointments, instead of what should be happening. They should be finding better ways to serve “the people “.

We pay these doctors great salaries and because NHS management have put such pressure on surgeries to self fund. This they do through clinics and other services but these are at the expense of the appointments systems.

There needs to be a complete re-think of the whole system and not by those who run it. There have been recommendations by some very good business owners but these have been ignored. Funding needs to be increased. A few pounds per month from each of us would still be cheaper than private medical insurance.

The NHS is one of the UK’s finest creations and admired around the world. Let’s at least make it possible to get a doctors appointment and cut out all the obstructions to do so.

The fight goes on

This week I had good news after my yearly bladder cystoscope. I am all clear of tumours. Then the bad news is because I have on going problems they want to do a bladder function test, which I have on the 24th. My problem is that Parkinson’s can also have an effect on the bladder functions. PD has been showing me this week it’s evil side and how despite my efforts to fight Mr P he is going to invade my life even more.

I have been having a clear out this weekend mainly the loft. Mr P had other ideas! Messing with my balance, strength, fatigue, thinking, and generally slowing me down. I have been trying to ignore it and carry on but it’s been hard. It been harder than ever before. I will not be beaten and despite waking this morning with cramps, stiff muscles all over I am going to carry on. I will not yet let it win. Trouble is I feel a new worsening of the affects of the PD which shows it’s progressive nature.

On a funnier note my memory is so bad I’ll most likely forget all the above by tomorrow. Another effect of PD with Lewy body.

I am staying positive and letting the light of positivity wash over me. There’s always something funny or happy in every moment of the day. I find that inner light to shine out no matter what. My next blog I’ll explore the skills needed to find peace and light to overcome Mr P.

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