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Partner seriously ill after baby, feeling like a single parent

86 replies

SilverLemon · 17/05/2026 21:01

Me and my fiancé welcomed our first baby in August last year. I've had about 2-3 months at the beginning of feeling like a team parenting our daughter and I'm so exhausted.

He was a completely healthy man before my pregnancy and I thought so during it but looking back the first symptoms and signs were starting. I put them down to the life changes we were going through and his father becoming terminally ill during my pregnancy and ultimately passing away two weeks after our baby was born.

Towards the end of my pregnancy and first few months following our daughter's arrival he was complaining of dizziness and then his legs feeling heavy when walking. In November he suddenly couldn't urinate all day and needed a catheter. A few days later he was in hospital with sepsis and since then it's all been down hill.

Luckily the sepsis was caught quickly and there was no organ damage or time in ICU, he was in hospital for over a week. But once discharged all his symptoms just amplified tenfold and have continued to get progressively worse.

I have now become his carer and feel like a single parent raising our daughter. He now cannot walk unaided and uses a Zimmerframe, he has regular falls at home, has essentially become housebound, his speech has changed, I'm pretty certain he is depressed and he can't really do anything for himself due to his balance issues. He wants to lay in bed all day, is awake all night and asleep all day.

I was ok at the beginning, believed it was just stress and that it would get better soon. But it hasn't. Two further hospital stays and lots of testing and we're still none the wiser of what's causing his symptoms. We know it's something neurological and he's now been referred to a specialist hospital, which we're still waiting to hear from. The delays in getting care and support are something I could dedicate a whole post too.

I feel like a single parent. I do everything for my daughter. He can't parent her right now, the best he can do is sit with her whilst he's in bed or when he occasionally comes downstairs which gives me 30 minutes to an hour to catch up on household tasks. Otherwise I'm with her all day doing everything. I know he wishes he could do more and I see how much this hurts him.

I'm just so exhausted. Being everything for everyone for over 5 months now. This wasn't how it was meant to be. We were supposed to be a team and equal. He was supposed to take her to swimming lessons, make her meals now she's on solids, take her for walks in the pram. I was supposed to get some breaks. Some time to try and reclaim some of my identity back, some time to feel like a romantic couple. My maternity leave has just been overshadowed by his illness. I'm going back to work in 3 months time and there's just so much uncertainty.

I just can't see the light at the end of the tunnel right now. It feels like he's dying. Every day I'm crying. But I can't talk to him and burden him further , I have to be the strong one but keeping it all inside is hurting me too. I feel suffocated by the responsibility of looking after him and our daughter. There's just no breaks. Sometimes I don't even want to be around him because it's so hard. I don't have any friends, just my mum and nan and the occasional message from a work colleague. He has no close family now, he's pulled away from his friends, they don't know how bad it is. He's currently on sick leave and I'm on the no money part of my maternity leave, just have savings now. That's another worry, finances.

Honestly there's so much more I could write but it would turn into a dissertation. I just need to offload and it would be comforting to hear similar stories. I feel so alone in my current reality and just unrelatable to any other new parents.

Thanks for reading.

OP posts:
Thread gallery
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RMAC67 · 18/05/2026 09:29

I’m so sorry you’re going through this OP.

I have MS, and it wasn’t picked up by the initial MRI. I had a second one with dye, and a lumbar puncture to finally get a diagnosis.
I would push for further tests, and i
hope you both get the answers.

There is great advice on this thread. Speak to
citizens advice first, and they will be able to tell you what help you’re entitled to. The pips system is awful, keep applying.

Wishing your family all the best 💐

ScaryM0nster · 18/05/2026 09:36

You are solo parenting and you are a carer. The carer bit is worth keeping in mind when you’re talking to your work as it comes with quite a few protections.

Periperi2025 · 18/05/2026 09:51

Without sounding like I'm writing your DP off, I think you need to look at all this through the lense of a solo parent. So long term work plan, childcare, finances and benefits.

Your situation is exactly what benefits are designed for, so really push for them and access them all.

What are his family doing to support him, can you get them more involved?

Could you, DP and baby move back in with family, so that you have more support with baby/ him or both.

As difficult as this is, you are not married, does your DP have a will or life insurance to protect you and your baby should the worst happen?

Are you in a union at work, the big unions (Unite, Unison etc) will have hardship/ benevolent funds for people in you situation?

Interested in this thread?

Then you might like threads about these subjects:

DaisyDooley · 18/05/2026 10:32

Do yourself a list of everything you NEED to do
1)PIP
2)Carers Allowance
3)Carers Uk (for support/advice)
4)Council- adult social services- get a social worker involved so you can get support. My husbands OT has been fab since we were allocated her
5)Sort out your return to work -who will look after baby? Who will look after DH?
6)Write down as it happens EVERYTHING to do with your husbands medical care. You may need this.
7) You need some self care. Can anybody look after baby for an afternoon just so you can have some ‘you’ time?
8) Get your shopping delivered. Meal plan easy meals.
9) Contcact your husbands friends, get them to come round and see him - and you go out.

The finances, your husbands health/day to day care care, the baby and YOU are the urgent things.

When my husband became paraplegic I found this group.
it’s a CIC , often on tv, run by a solicitor. I couldn’t have managed to get PIP without them. https://www.fightback4justice.co.uk/?fbclid=IwY2xjawR3uYNleHRuA2FlbQIxMABicmlkETFQaTd1REZJNGFmeG5mVXVrc3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHh2gVSVtziG6nsPI2bB_CsO7_jT2MOPAU8rgutHeh6Zyjoklkt9kZbbx1RXD_aem_oDksf-QV6R2SjkvnFi6BBg

They are amazing.
Do not be worried about asking for help. You have a massive burden on your shoulders and you need help.
Your husbands health issues may not be permanent. Just get through today, tomorrow, this week.
But please please try to get some support. I drove myself to a breakdown doing everything.

https://www.fightback4justice.co.uk/?fbclid=IwY2xjawR3uYNleHRuA2FlbQIxMABicmlkETFQaTd1REZJNGFmeG5mVXVrc3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHh2gVSVtziG6nsPI2bB_CsO7_jT2MOPAU8rgutHeh6Zyjoklkt9kZbbx1RXD_aem_oDksf-QV6R2SjkvnFi6BBg

Crwysmam · 18/05/2026 12:27

Sometimes life hits hard. All your plans and hopes are dashed and it is very difficult not to resent the person who you thought was going to be your biggest supporter and cheer leader. Instead you spend your time just keeping your head above water.

Even with all the help in the world, financially and physically it’s hard to see a future.

I was diagnosed with breast cancer 4 yrs ago., 2 mnths after I finished treatment my DH had a stroke. We are at the other end of life to you but had so many plans for our retirement after working hard and bringing up a family.

It has been tough. DH made a good recovery but was unable to work after his stroke. We were in an incredibly fortunate position though, I had just sold my business, and we were both able to retire early on a good joint pension income.

But what people don’t get is the emotional strain it has put on our lives. The constant guilt I feel about doing stuff without DH. He was about to have an essential knee replacement at the time of his stroke, it would have made life so much easier. His rapidly deteriorating mobility post stroke meant he had become depressed and demotivated.

A week ago he had his knee replaced. It’s early days and he’s still in pain but already I can see the improvement in his mood. Despite the pain he can climb the stairs in half the time he took pre op. I am very much his carer at the moment. I have to help him dress and carry everything around for him. But I’m optimistic that this time next year we will be able to enjoy all the things that we haven’t been able to consider doing for the last 10yrs.

I just hope it’s not too late for him to regain his love of life again. Chronic illness is draining for the sufferer and their carer. It can be very difficult to see a future. It’s easy, from the outside, to feel that financial support is the answer but the impact on your mental wellbeing is probably more important.

My DH is acutely aware of how my ongoing breast cancer treatment impacts on my health. To the outside world I’m fit and well, I’m not, the meds I take can floor me at times. He encourages me to take time out so that I can decompress. He can cope for a couple of days, so that I can have a break.

Try and get some respite, arrange for someone to spend time with your DH so you can have a break. Ask for help before it destroys your relationship.

BridgetJonesV2 · 18/05/2026 13:09

The tests coming back as negative jumped out at me, in honesty.

Do you think there is a chance he's playing on this OP?

Because in truth, I'm not sure that you can do 100% of the grunt work here and stay sane/well.

sunshinestar1986 · 18/05/2026 13:40

BridgetJonesV2 · 18/05/2026 13:09

The tests coming back as negative jumped out at me, in honesty.

Do you think there is a chance he's playing on this OP?

Because in truth, I'm not sure that you can do 100% of the grunt work here and stay sane/well.

It's probably FND

SilverLemon · 18/05/2026 15:16

BridgetJonesV2 · 18/05/2026 13:09

The tests coming back as negative jumped out at me, in honesty.

Do you think there is a chance he's playing on this OP?

Because in truth, I'm not sure that you can do 100% of the grunt work here and stay sane/well.

Absolutely not. The difficulties he's facing, no one could put them on. He's got confirmed clinical signs of neurological deficits.

OP posts:
SilverLemon · 18/05/2026 15:20

Crwysmam · 18/05/2026 12:27

Sometimes life hits hard. All your plans and hopes are dashed and it is very difficult not to resent the person who you thought was going to be your biggest supporter and cheer leader. Instead you spend your time just keeping your head above water.

Even with all the help in the world, financially and physically it’s hard to see a future.

I was diagnosed with breast cancer 4 yrs ago., 2 mnths after I finished treatment my DH had a stroke. We are at the other end of life to you but had so many plans for our retirement after working hard and bringing up a family.

It has been tough. DH made a good recovery but was unable to work after his stroke. We were in an incredibly fortunate position though, I had just sold my business, and we were both able to retire early on a good joint pension income.

But what people don’t get is the emotional strain it has put on our lives. The constant guilt I feel about doing stuff without DH. He was about to have an essential knee replacement at the time of his stroke, it would have made life so much easier. His rapidly deteriorating mobility post stroke meant he had become depressed and demotivated.

A week ago he had his knee replaced. It’s early days and he’s still in pain but already I can see the improvement in his mood. Despite the pain he can climb the stairs in half the time he took pre op. I am very much his carer at the moment. I have to help him dress and carry everything around for him. But I’m optimistic that this time next year we will be able to enjoy all the things that we haven’t been able to consider doing for the last 10yrs.

I just hope it’s not too late for him to regain his love of life again. Chronic illness is draining for the sufferer and their carer. It can be very difficult to see a future. It’s easy, from the outside, to feel that financial support is the answer but the impact on your mental wellbeing is probably more important.

My DH is acutely aware of how my ongoing breast cancer treatment impacts on my health. To the outside world I’m fit and well, I’m not, the meds I take can floor me at times. He encourages me to take time out so that I can decompress. He can cope for a couple of days, so that I can have a break.

Try and get some respite, arrange for someone to spend time with your DH so you can have a break. Ask for help before it destroys your relationship.

Edited

Thank you for sharing your story. I really hope things continue to move in the right direction for you and your dh

OP posts:
violetcuriosity · 18/05/2026 15:24

Have his brain and spinal MRIs come back clear? I’ve had acute transverse myelitis and had the exact same clinical picture but was treated quickly. Have they attempted IV steroids/IVIG/PLEX? I’m assuming antibody testing has been done?

Confuserr · 18/05/2026 15:27

SilverLemon · 18/05/2026 15:16

Absolutely not. The difficulties he's facing, no one could put them on. He's got confirmed clinical signs of neurological deficits.

Indeed, noone can "fake" sepsis!

SilverLemon · 18/05/2026 16:55

violetcuriosity · 18/05/2026 15:24

Have his brain and spinal MRIs come back clear? I’ve had acute transverse myelitis and had the exact same clinical picture but was treated quickly. Have they attempted IV steroids/IVIG/PLEX? I’m assuming antibody testing has been done?

Yep, he's had brain/spine MRI twice now, 2 months apart, all normal. He's had antibody testing which has been negative, some more actually came back through today that were sent off months ago for encephalitis which were all negative.

Nope, they've not attempted any sort of treatment, it's very frustrating.

OP posts:
Trotula · 18/05/2026 21:17

What an awful situation for you to be in at a time when you need help.
Have they considered Gillain Barre syndrome? I don’t think it is easy to diagnose but does present with some of the symptoms you’ve described.
https://www.nhs.uk/conditions/guillain-barre-syndrome/
Can DH family support you in any way?

nhs.uk

Guillain-Barré syndrome

Find out about Guillain-Barré syndrome, including its symptoms, how it's treated, how long it takes to recover and when to get medical help.

https://www.nhs.uk/conditions/guillain-barre-syndrome/

putitonthewrongway · 18/05/2026 21:51

I’m so sorry for what you are going through I have no great advice just lots of sympathy 💐 I went through something similar last year when my husband had terminal cancer (I am not in any way suggesting that your partner has cancer). But I mean in the sense of being in a carer role and being a mother to a five year old and a 1 year old. It was horrific and relentless. I felt pulled three ways and I felt like I was doing a rubbish job of looking after all of them.

I don’t live in the UK, so my suggestion might not be useful, but I would suggest getting signed off work with stress until you can get your life into some kind of order. It takes a while to adjust to being the only one able to parent but I promise you will adjust and it will become the new “norm” (though I’m not saying it’s easy).

You have been dealt a really shit hand but do not lose hope. Best of luck I hope he gets his diagnoses soon and he is able to receive some treatment 💐

peppaispoop · 18/05/2026 21:55

Are you sure he’s not having you on?

putitonthewrongway · 18/05/2026 22:06

peppaispoop · 18/05/2026 21:55

Are you sure he’s not having you on?

The OP says he had sepsis and confirmed signs of neurological deficits

Penkie · 18/05/2026 22:09

I think that getting a diagnosis has to be the priority because from there, you can apply for all sorts of support.
I would go to the doctor with a list of "Could it be this" possibilities explaining which symptoms are making you question this.
It's a very challenging situation for you, and I hope things change soon.

Crispynoodle · 18/05/2026 22:10

You need carers can you refer yourselves to social services?
also bizarrely this sounds very much like a person I know who suffered a spinal stroke (even as an ex nurse I had never heard of them)

OpheliaNightingale · 18/05/2026 22:25

Please get him to have his vitamin B12 checked.

Velvetgoldmine · 18/05/2026 22:29

Please ask them to check for MSA. The symptoms sound very much like those my partner had. MSA is hard to diagnose, but can present initially like Parkinson's. If you would like more info on symptoms please message me.

springy0c · 18/05/2026 22:30

Sounds like myasthenia gravis an autoimmune disorder can be diagnosed by a simple blood test and treatable with medication

violetcuriosity · 19/05/2026 07:28

SilverLemon · 18/05/2026 16:55

Yep, he's had brain/spine MRI twice now, 2 months apart, all normal. He's had antibody testing which has been negative, some more actually came back through today that were sent off months ago for encephalitis which were all negative.

Nope, they've not attempted any sort of treatment, it's very frustrating.

I think it might be time to start pushing for steroid treatment as a first port of call just to see if there is any response- I had 3 days of IV methyl prednisone and have been on a tapering dose for the last 7 weeks. It is well known that anitbodies do not always show, especially if the inflammation is subtle enough to not show on MRI (not minimising the symptomatic impact). Can you ask for a referral to John Radcliffe in Oxford or the one in Liverpool if you’re closer? I think it’s time to start becoming a complete pain in the arse. I had to go back to A&E 5 days in a row before I was taken seriously and luckily had very efficient care after that.

On a side note, I had antibody tests sent off to Oxford 7 weeks ago, how many weeks did your husband’s take to come back? The wait is awful.

SilverLemon · 19/05/2026 08:08

violetcuriosity · 19/05/2026 07:28

I think it might be time to start pushing for steroid treatment as a first port of call just to see if there is any response- I had 3 days of IV methyl prednisone and have been on a tapering dose for the last 7 weeks. It is well known that anitbodies do not always show, especially if the inflammation is subtle enough to not show on MRI (not minimising the symptomatic impact). Can you ask for a referral to John Radcliffe in Oxford or the one in Liverpool if you’re closer? I think it’s time to start becoming a complete pain in the arse. I had to go back to A&E 5 days in a row before I was taken seriously and luckily had very efficient care after that.

On a side note, I had antibody tests sent off to Oxford 7 weeks ago, how many weeks did your husband’s take to come back? The wait is awful.

Yes, I'm going to ask for that. He has his neurology appointment in a couple of weeks.

He's been referred to UCLH neurology following his last admission last month, but still waiting to hear back.

I've just looked and it was over 11 weeks for the antibody testing results.

OP posts:
SilverLemon · 19/05/2026 08:09

springy0c · 18/05/2026 22:30

Sounds like myasthenia gravis an autoimmune disorder can be diagnosed by a simple blood test and treatable with medication

Had a blood test for that ordered by the GP, negative unfortunately as when I looked it up it did fit a lot of his symptoms

OP posts:
springy0c · 20/05/2026 08:45

SilverLemon · 19/05/2026 08:09

Had a blood test for that ordered by the GP, negative unfortunately as when I looked it up it did fit a lot of his symptoms

10 to 15 per cent of cases don’t show up on blood tests. Something to be aware about when discussing with consultants