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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:
KPPlumbing · 21/08/2025 20:42

Rainbowqueeen · 21/08/2025 19:53

That’s really tough OP.

Sending hugs. Please go and see your GP. HRT was life changing for me.

I'm sorry, but how on earth will HRT help the OP, with the very real, logistical, practical and emotional difficulties she faces every day?!

She's dealing with a profoundly challenging set of circumstances. It can't be treated with hormones!

MynameisJune · 21/08/2025 20:42

@Montereyjaaack I’m so sorry life dealt you and your DD such a shitty hand. And I’m sorry that funding for social care is absolutely abysmal.

It’s okay to admit that you’re living a bit of a nightmare, absolutely no one would blame you. You can love your DD and also despair at the situation. I wish I could solve your problems but I know how shit services are in the Uk for disabled people.

Seawolves · 21/08/2025 20:46

Destiny123 · 21/08/2025 20:35

Sorry to hear

Approach your council for short breaks respite, you'll be entitled to 1 weekend a month, I'm about to become a respite foster carer

www.gov.uk/apply-short-term-care-for-child

Ask for a different format or iron, some cause diarrhoea/constipation/nothing

Xx

That's a lovely sentiment but foster/LINK carers are thin on the ground in most areas.

My little one is entitled to quite a lot of continuing healthcare hours but we can't find the carers to offer the care package he's entitled to and I have been looking for carers for over a year.

Montereyjaaack · 21/08/2025 20:48

Thank you all. I guess it’s not an AIBU but sometimes I think am I just being weak?

I adore my DD - she’s hilarious, she’s full of life and (I know it makes no sense to say she’s hilarious if she’s nonverbal but she is, very hard to explain). I love her cuddles. I love her little face. She is my entire world. I just sometimes wish there could be practical help once a month or something.

Re the council carers - I’m working on the uselessness but it’s complex and I’m just worn out trying to fix something that’s meant to be a solution!

I understand the suggestion of residential care but until I am far far too unable to function that would never be a solution. She needs me and we have a wonderful bond. It’s just tough some days

OP posts:
Komododragonchocolatecoin · 21/08/2025 20:51

I used to think disabled children and their carers got loads of support...until I had a disabled child. No one gives a shit and the benefits cover next to nothing. It sucks. We had a good day today. I wish you one soon xx

Hohofortherobbers · 21/08/2025 20:51

Im so sorry, your situation is heartbreaking. You have worries already about what her long-term care will be, can you investigate these now and start making connections. Would council fund a residential place for her now?

thequeenoftarts · 21/08/2025 20:51

Your post is heart rending to read. I'm very sorry that it is so hard for you both. I do think think you are blooming amazing and your daughter is so lucky to have you in her corner. No, you are not unreasonable, you are the one left holding the baby literally, while everyone else gets to live their lives. I don't have the answers for you, but I wanted to send you 🌻 flowers as I think your child is blessed to have you as her Mum.

NotbloodyGivingupYet · 21/08/2025 20:54

KPPlumbing · 21/08/2025 20:42

I'm sorry, but how on earth will HRT help the OP, with the very real, logistical, practical and emotional difficulties she faces every day?!

She's dealing with a profoundly challenging set of circumstances. It can't be treated with hormones!

It might just help her feel a little bit more able to cope. It's one aspect of the Ops life that maybe someone can help her with. Don't beat up people who are trying to offer help.

likeafishneedsabike · 21/08/2025 20:54

I have no expertise or advice but my heart goes out to your. Your post makes me want to jump in my car and come to help you.

tothelefttotheleft · 21/08/2025 20:57

I wish people who don't live with this reality wouldn't talk about respite or residential care.

Don't you think someone living like this has explored those options?

LoveSandbanks · 21/08/2025 20:58

DarkFate · 21/08/2025 20:10

I’m not to big to admit I would put a child with those significant needs in residential care, and go and see her everyday instead/take her out when I could.

It’s not that easy anymore. You’d then get charged with child abandonment!

it wasn’t that long ago when it would be almost unthinkable that a severely disabled child would remain in the family home. Now I’m not sure there are any facilities available at all.

LoveHearts69 · 21/08/2025 21:00

I have NT young children with no family help and that’s hard enough, my heart really goes out to you because this does sound so bloody tough. That’s awful that you don’t get respite. Sending hugs and if you were my friend I’d love to help. Maybe reach out to friends if you can, they might be more willing to help than you think ❤️

Montereyjaaack · 21/08/2025 21:03

I can’t respond to you all individually but I appreciate everyone. MN is great sometimes!
re HRT - I can’t take oestrogen (I know that sounds daft but there’s a reason) and I definitely would try it. I’m a year off Sertraline (and very glad to be!) which was GP’s suggestion. It didn’t help at all.
I really really wish there was structured support- outside the hospice scene - because I do valued the occasional night’s sleep right through while knowing she had nurse professionals able to do what she needs.
And nothing sadly alleviates the fear of the future.
I often fantasise about moving to a country where care provision would be better but I really don’t think it exists!
I remember watching Colin Farrell talking about his disabled son and what he does for him and his setting up a foundation for disabled kids and their families and thinking I wish I had the wherewithal to do that for UK families

OP posts:
Wowwee1234 · 21/08/2025 21:04

SleeplessInWherever · 21/08/2025 20:34

Most people with high needs kids can’t access reasonable respite care, nevermind residential.

I think most people actually wouldn’t put their kids in residential anyway tbh. In reality, you want to keep them safe at home with you and keep battling on, for as long as possible.

That's unfair. Residential care can be amazing and helps many people with very difficult situations, although not for everyone obviously.

Glassmatt · 21/08/2025 21:06

Life isn’t fair and it’s situations like this that should make people realise how lucky they are. I’m so sorry this is your life and the life of your LO. It’s sickening to think you feel utterly deserted because there is no funding to help. Even if there was respite care once a week so you got time to yourself to recharge

Robin67 · 21/08/2025 21:08

Nothing about you is unreasonable. You are a literal superhero in my eyes. 🌺

carly2803 · 21/08/2025 21:08

I have no advice OP but I just want to say I think your doing an amazing job. Working with a broken system is not easy.

Your daughter is lucky to have you, and all that you do for her.

Destiny123 · 21/08/2025 21:10

Seawolves · 21/08/2025 20:46

That's a lovely sentiment but foster/LINK carers are thin on the ground in most areas.

My little one is entitled to quite a lot of continuing healthcare hours but we can't find the carers to offer the care package he's entitled to and I have been looking for carers for over a year.

Depends on the area some have v little/no waiting lists, always worth a try contacting

https://www.surreycc.gov.uk/children/support-and-advice/children-with-disabilities/short-breaks

I'll be offering 2-3 weekends a month (Dr so work 1 weekend a month) as soon as I'm approved to help as many as possible

Surrey short breaks for disabled children - Surrey County Council

Find information about what Short Breaks are, what we have on offer, our Short Breaks statement and links to other services we have to offer.

https://www.surreycc.gov.uk/children/support-and-advice/children-with-disabilities/short-breaks

Destiny123 · 21/08/2025 21:12

If Surrey based (or kent) happy to help

Destiny123 · 21/08/2025 21:16

Seawolves · 21/08/2025 20:46

That's a lovely sentiment but foster/LINK carers are thin on the ground in most areas.

My little one is entitled to quite a lot of continuing healthcare hours but we can't find the carers to offer the care package he's entitled to and I have been looking for carers for over a year.

See the link above but in our area you don't have to find carers the council has a list of people they match you with and provide 24 overnights a year of respite care

ItalianRedParka · 21/08/2025 21:19

SleeplessInWherever · 21/08/2025 20:34

Most people with high needs kids can’t access reasonable respite care, nevermind residential.

I think most people actually wouldn’t put their kids in residential anyway tbh. In reality, you want to keep them safe at home with you and keep battling on, for as long as possible.

In my experience they can. I used to work in nhs commissioning. It's hard but not undoable

x2boys · 21/08/2025 21:20

tothelefttotheleft · 21/08/2025 20:57

I wish people who don't live with this reality wouldn't talk about respite or residential care.

Don't you think someone living like this has explored those options?

It's everytime ,there is thread like this respite and residential school, s are mentioned i would be embarrassed to post about something I knew nothing about but it doesn't stop posters and certainly doesn't help the Op.

Hellenbach · 21/08/2025 21:20

Sorry you’re finding life so overwhelming. The school holidays with a SEN child are exhausting. I’m a lone parent and I’m on my knees at this point.
I’ve got a Mencap case worker who can’t do much other than listen but I feel it makes a difference.
If it’s affordable I’d suggest therapy sessions, just so you can offload to a non-judgemental person and dump all your worst fears and anxieties.
It’s a tough path for sure.

x2boys · 21/08/2025 21:21

ItalianRedParka · 21/08/2025 21:19

In my experience they can. I used to work in nhs commissioning. It's hard but not undoable

It's extremely hard and not something the Op wants anyway.

hattie43 · 21/08/2025 21:24

I take my hat off to you . I know I wouldn’t be able to deal with this at all .

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