This is what you voted for

I will no longer be able to have my LifeLine care alarm due to an increase in the weekly cost of the service.

While I have never had to use it I have come close to pressing that little red button many times, and it has given me such peace of mind during my poorliest days to know that pressing a simple button will automatically get a message to Mr Tree Surgeon, my Wonder Mum, or as a last port of call the emergency services.

I have paid 18p per week for what is surely a life saving service for so many people. The cost is increasing to £1.50 per week, which will be £78 per year. Not a massive amount of money but I’ll remind you that I am on disability benefits; benefits that I live in constant fear of having taken away from me. (So worried and conscious of money am I that I no longer take the whole host of supplements that may well help with my health condition because I’m just cannot afford to financially.)

I can raise the issue of affordability with the Council but I would rather any subsidies went to those who need such a service far more than I do.

“despite the unprecedented financial pressure the Council is facing, [the £1.50] continues to be less than the cost of providing the service.”

From my understanding, the council have taken on the majority of the cost of these alarm systems but because of cuts to their own funding, they are no longer able to do so on the same scale. Hence why each service user is being asked to pay what is quite a considerable bit more.

What saddens me most is that there will be people who rely on these LifeLine alarms in a way that I do not have to. It is likely that they too though are unable to afford to keep their alarm systems because of the increase in cost. I am not writing this post as a sob story or for sympathy, but simply to highlight what it happening to some of the most vulnerable people in society. I am incredibly lucky that having my LifeLine machine will not impact too heavily on my ability to call for help. Touch wood. During my bouts of paralysis I am unable to press the emergency button anyway. And I have grown so used to riding out crashes and then texting for help (if I’m suffering more than I can handle alone) when I am able to function enough to do so.

The majority of people in our little country will be oblivious to things like this. Lucky them. Ignorance sure is bliss.

Published by Anna Redshaw

Blogging about life in the slow lane with an invisible, chronic illness. I wasn't always a sick chick so this is somewhat of a life changing experience!

4 thoughts on “This is what you voted for

  1. I hate the fact that we even use telecare. Where I live all they do is phone my already exhausted partner who is meant to drop what she does and rush to my attention.. the reality is she can’t drive and is often two bus rides away.. the result being social services send police ambulance and fire service along as they don’t know what I need… last time I had got stuck on a commode, I haven’t used it since… I didn’t need all the emergency services to get me off the commode… but council policy is to contact the emergency services.. the red button doesn’t give me any peace of mind… a carer would.


  2. I’m sorry you have to go through this. My grandma has a Life Alert care service too and I can’t imagine her living alone without it because of financial reasons. Good luck to you in everything, things will get better!


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