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AIBU?

Share your dilemmas and get honest opinions from other Mumsnetters.

To be so fed up - today - of being a parent to a disabled child

231 replies

Montereyjaaack · 21/08/2025 19:46

I’ve NC for this. Sorry this is very long.

i adore my DD. She’s so brilliant in every way she can be. But I’m so utterly fed up of lack of sleep, lack of support and lack of money.
Im also so sick and tired of the shit I see from people online whinging about disabled people and benefits and “free” cars etc.

I want nothing more than for my daughter to be safe and happy. I’m sick of worrying about her future. I’m sick of services stopping or not being available in the first place. I’m sick of not being able to have a proper income or a satisfying job.

Im terrified of what will come if her when I die. I’m already 50 and she’s not yet 10. She’s non-verbal, can’t use ANY communication systems (PECs, signing or technology). She can’t walk. She can’t stand. She can’t eat.

Shes probably autistic but is just in a waiting list and the assessment probably won’t mean much because they admit they don’t know how to assess her.

She has no respite. So-called carers provided by the council for 6 hours a week are beyond useless and more of a burden to me than she is.

Everything is a struggle - everything. She doesn’t sleep more than 5 hours and makes so much noise when she wakes. There are safety issues around her inability to swallow safely so someone had to keep an eye of actually intervene to suction her during the night to add to the joy.

I’ve had to wash her bedclothes every day (plus clothes etc) this past week because she had iron medication (as she’s anaemic) and flooded her pads with diahorrea that burst into her bed, her duvet etc.

No family help (I have a husband but less said about that the better) as family are older/in different countries.

The hospice she received support and respite overnight a couple of times a year has discharged her as she’s apparently lucky she isn’t likely to die before18. So Jo overnight care ever unless something magical happens to the UK economy.

There are no actual respite services in this county. I couldn’t afford private respite even if it did exist as I work 10 hours a week in term time and only started that before Christmas last year so haven’t been able to save. And then have carer’s allowance and child benefit.

She loves being out and about- so I have to have a WAV from Motability- so all the mobility component of DLA goes on that . Then petrol - already £200 over summer holidays. We are limited as to where we can go because she’s doubly incontinent so very very limited time out and where there are changing facilities to hoist her.

I am generally a cheerful person but now in perimenopause so I’m just reaching my fucking breaking point with a period that is so heavy I feel faint all the time but still have to go and go and go because she’s so limited - she can’t play with toys or use a tablet because of how her physical limitations affect her.

I am so sick of trying to stay afloat. I used to have a fairly well paid job. I used to have time to myself. But this is it until we are both in wheelchairs or care or something equally shit.

It probably isn’t an AIBU but am I unreasonable for feeling this is it? It doesn’t get better does it?

OP posts:
Seawolves · 27/08/2025 20:56

@Montereyjaaack We are fortunate that he when he qualified for mobility on DLA we were awarded a wheelchair vehicle with a hoist and a seat that converts to a changing bed in the back, it took almost 18 months to arrive (to the point where his DLA was due for renewal before we took delivery) but now we have it it has been an absolute godsend.

I hear you on the overnight care. It's the broken nights I find the hardest, between pain, needing suctioning, seizures, vomiting, his bloody feed pump malfunctioning, needing to turn him, giving his meds at midnight and his random "let's party" awakenings I am running on empty some days.

Holmints · 27/08/2025 21:02

Seawolves · 27/08/2025 20:06

Our Tonie box is a lifesaver sometimes, some of the Enid Blyton ones play for hours!

There’s a Tonie 2 about to be released with more night time features too. Wish I’d invented them!

Montereyjaaack · 28/08/2025 06:30

She had a Toni box when she was younger - it stopped working very quickly for some reason (I mean it broke) and we didn’t replace it because she was never keen. Part of her problems are her repetitive interests.
She stopped watching new cartoons or films when she was 5 and won’t watch anything new - she’s actually slept a bit better tonight but woke me up crying because something she didn’t know came on her Kindle Fire (she swiped it and sometimes it puts different shows on.
@Seawolves - I had no idea WAVs like that even existed! We’ve been trying to find a powered wheelchair that lies flat. Actually tested one yesterday but she’s still too small to use it so back to the drawing board on that

OP posts:
Anewuser · 29/08/2025 10:31

@Montereyjaaack please don’t take this the wrong way because I know you say she’s had genetic testing but was it Whole Genome 100,000 sequencing? It took us years to finally get a genetic diagnosis, and whilst it doesn’t change anything, at least we have an answer.

@Seawolves that WAV sounds amazing and exactly what we’ve always needed. We bought a mobile hoist so we could hoist him onto the floor of the wav but then he got too big for that. Our motability contract is up in November so we’re looking now. Please would you mind telling me what you have? TIA.

Seawolves · 29/08/2025 11:10

@Anewuser A VW Crafter and the conversion was done by Brook Miller, the seat under the hoist pulls down into a bench.

To be so fed up - today - of being a parent to a disabled child
Anewuser · 30/08/2025 13:12

@Seawolves that's really useful, thank you.

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