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- when you see your dream car at the village day car show and you wish they did cars like this on the mobility scheme.unfortunately because you’re visually impaired you cannot drive but you imagine you and your PA cruising around in this sort of car in this colour with the top down music blurring and having a rave in your car Scheme to bring this car out on it this was back in July when I went to my local village day
- Family Allergies Prevent Woman Getting New Guide Dog
- Little mermaid meet greet from the mermaid herself at my local village day 2026 this is what the right amount of funding means that you can live and have an amazing experience is like rather than just dreaming about having them and seeing other people on social media having them while you are not this is why Ifight for my right to freedom and independence. If you Battle continue fighting that war because when you’re out the other side of it well at least your first war you will be grateful that you fought it. I’m living proof that you will be grateful for the fact of people that honestly just didn’t want you to have freedom and and independence telling you that it wouldn’t be possible due to your name who make decisions about funding and allocation of your care and support budgets
- Canada Puts Assisted Dying Expansion For Mental Illness On Hold
- enjoying participating in life again after spending 11 months to one year not being able to do anything due to lack of funding and the diagnosis of FND and before that not being able to do anything because regardless of FND for six years I had An adequate package and inadequate funding for support and a care agency that actually didn’t Care LOL they said they were Care agency to Care and actually didn’t give a shit but now I’m with my own PA who I have control your Over who gets employed with me and who I want and who takes care of me and what skills I want them to have to be employed with me this is what good support means accessing life again and being included rather than exluded this access to life is something I thought I would never regain again but here is me accessing life back in July when I decided to go to my Caribbean social club Having a cup of tea because whoever who has got to know me will know that me and T are a perfect pair where there’s me there’s a cup of tea To a point where our infections are so high that we honestly don’t know whether we are going to live or not for this access to life to be given back to us it’s disgusting and local authorities need to give equal access to funding for our Carers/PA Us getting so ill they should think about preventing illness not firefighting it after it happens but I’m still grateful and glad for the access to life again I appreciate every single moment of access to life I have But I would appreciate it if we didn’t have to get to a point where we were so sick that we were wondering whether we were going to be a live or not for them to take action yet if I lived in a county next door to me Access the funding and the access to funding for PAs and Carers needs to be standardised wherever you live in the UK post code Lottery thing is bullshit in my opinion and needs to stop
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