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Virginity, Sex, Disability and Safety.

By Disability, The Love Lounge

The Question

Hello,

I tripped upon your organization while looking up sex and cerebral palsy on YouTube. I’m writing to you about losing my virginity, sex, disability and safety.

I am 51 years old, spastic quadriplegic born with cerebral palsy and use a power wheelchair for mobility. I’ve had a couple crushes when I was a teenager and in college but that was it. My parents never talked to me about sex other than the most basic education of how one becomes pregnant and the high school sex Ed.

I would like to experience sex before I die, but I also don’t believe in sex unless I am in a long-term relationship. I have been struggling for many years with several health challenges that have made my cerebral palsy worse and left me with unmanaged chronic pain. Due to my multiple health challenges and many family issues I do not have the ability or interest to go out to bars. I am also scared about my safety in dating a man. For example what do I do if I want to have a little privacy to be intimate but due to disability you can’t get away if it becomes more than you want and the other person doesn’t respect that. What do you do?

I’m really embarrassed to email you this but thankful that there is this platform. I feel like a freak!

G x

 

Our Answer

Hi G,

It took great courage for you to write into us and I’m so glad you reached out. I can feel your predicament here in being caught up in a bit of a moral dilemma. Also, you have some big practical issues which are making it more difficult for you.

It would be useful to know more about your family issues which you say are urgent and making it less likely for you to go out. Understanding this, I may be able to see how you could overcome this. Also, if you have any carer that works with you. As they may be able to facilitate you getting out socially and also make you feel safer if meeting someone.

Hearing your concerns, it seems to me that it comes down to a choice of what is your biggest priority now. Is it about losing your virginity? Or is it doing the act within a long-term relationship or marriage?

Currently, with the situation as you describe, it sounds like it will be difficult for you to be getting out and meeting someone. This can take a lot of  effort at the best of times, so with your family difficulties, meeting the right person could take even longer.  Are you willing to wait quite a while longer to lose your virginity within a loving relationship?

If you don’t want to wait, there’s the option of seeking out a sexual encounter, perhaps not in a relationship. This is where it would completely depend on how you feel going against your current beliefs about the parameters within which a sexual relationship should be conducted.  And if you feel you would be comfortable undertaking such an experience.

a graphic of a mobile phone with a person and lovehearts in white and the background is pink

In the UK a charity called TLC have sex workers who work with disabled clients. Exactly for the reasons you say. They guarantee safety and can offer a ‘boyfriend/girlfriend experience’ too. Here is the link to their website. https://tlc-trust.org.uk/

It may be that you could take it slow and steady rather than going full steam ahead on the first time.  There is a cost to this service and it’s quite expensive but the workers are trustworthy and experienced in working with disabled clients.

If this isn’t a consideration for you, maybe try internet dating to try and engage with someone, building a rapport before taking it further. Again, if you have a friend or a carer you can trust, they could go out with you the first time you meet your date. You mention your fear around someone wanting to go further than you want, and how do you stay safe. You’re right, we are more vulnerable as disabled daters and have to think of more options to keep safe.  I would suggest a friend or carer being in the same location as you, but not sitting near you to allow you some privacy and normality for you and your date. If you needed help,  your friend can keep an eye on things and it would be easy to catch their attention. They can then ‘rescue’ you from any awkward situation.

With internet dating there’s another dilemma we all face. Do we declare our disability openly and attract those who are open to dating someone disabled? Or don’t declare it, attract more people, get talking to some people first, then drop the disabled bomb?!

The world of dating and disability can be a minefield. But it can also be fun. Losing your virginity is an important human right and feeling stopped from doing so is deeply frustrating.  Ultimately, it’s your choice with how you wish to go about it.  I just hope your current living situation allows you to make a free choice. It is your body and your life after all. Do what feels right for you.

Best regards,

Zoe

Keep up to date with all Love Lounge chat and our campaigns by connecting with us on twitter @ETUKUndressing or on Instagram @UndressingDisability  

If you’d like to get our experts advice with your own dilemma feel free to get in touch. 

 

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Stress Impacts Your Libido - a face covered with hands and another two hands pressing down on the side of the head

How Stress Impacts Your Libido and General Health

By Disability, Undressing Disability

This article is about how stress impacts your libido and general health.

What is stress?

When we’re feeling stressed, our body has a physical reaction which triggers the release of cortisol and adrenalin. These stress hormones send us into what is known as ‘fight or flight’ mode. Instead of being relaxed we are on edge, worried or overwhelmed. Everyone has different things that trigger stress but for the majority of people stress impacts your libido, your mental health, and your physical wellbeing.

Physical Symptoms of Stress

Stress is exhausting and lowers our tolerance for many things. Some symptoms of stress are:
• Sweaty palms
• Foggy mind and/or irrational thinking
• Irritability and/or low mood
• Rapid heartbeat
• Shallow breathing
• Insomnia

When stressed, we just don’t have the capacity to be thinking about others, only focussing on ourselves. A lack of tolerance for others, irrational thinking and even aggression can impact our relationships by pushing your partner away. In turn, the lack of closeness can lead to more worry about your relationship and perhaps lead to low self-esteem.

Stress and Libido

Stress can affect both men’s and women’s libido. The stress hormone cortisol disrupts your testosterone levels, which is responsible for men and women’s sex drives. It can also:

• Narrow your arteries, meaning men may experience erectile dysfunction
• Take you longer to become aroused and reach orgasm

When you’re stressed and have worries and thoughts running through your head it’s not surprising that your libido might decrease.
If stress is impacting your libido, trust that this can change. It doesn’t mean your sex drive will be low forever. It can fluctuate at any time and for many reasons. Intimacy may help reduce your stress too. So kisses, a loving cuddle or massage can alleviate your tension and stress. And with time, this may help your libido increase.
Masturbation can be a big stress reliever too, so it’s not just a partner that can make you feel good!

What can we do to manage stress?

When you feel stressed and are aware of the physiological changes, try and take control back by refocusing your thoughts. Ask yourself:

1. What is really going on in this moment?
2. How can I reasonably respond to the situation?

This isn’t easy and will take much practice to regain control of your thoughts.

Here are some tips:
• Slow down your breathing and breathe through your nose, deep into your belly, expanding your diaphragm. Release the breath slowly and forcefully, emptying the lungs.
• You can use mindfulness with your breathing too. Notice the air flowing through your nostrils and how your chest and belly rises. How does it feel? This exercise of thought focus will divert the panic response of fight or flight.

Managing relationships whilst stressed

If you recognise that you’re being snappy and impatient with your loved ones, don’t be too proud to admit it’s happening.
When you’ve got time to collect your thoughts, be honest with them. Say

‘I’m stressed at the moment and know I’m being irritable. Bear with me’.

This will help dissipate their bad feelings towards you, rather than you not admitting it, feeling guilty yet still displaying the unhelpful behaviours! Also just being open and chatting the problem over with them may help you. The old adage ‘a problem shared is a problem halved’ is so true.
• Always remember – talk, reach out, use techniques, seek support! It’s out there.
• Speak to your doctor if stress is impacting your day to day life.

Useful Resources

The Stress Management Society – 30 Day Challenge

Mental Health Foundation – How to Manage Stress

NHS – 10 Stress Busters

 

Keep up to date with all our Undressing Disability chat by joining us on twitter @ETUKUndressing or on Instagram @UndressingDisability.

A woman with a disabled partner - she has brown curly hair leans down and puts her arms around a blonde man in a black top, they look lovingly at each other and smile

Family Reaction To My Relationship with a Disabled Guy

By Disability, The Love Lounge

The Question

Dear Love Lounge,

I need your advice on my family’s reaction to my relationship with a disabled guy. My parents have met my partner numerous times over the past year, and we all get along well. Last month we moved in together and plan to get married. My Dad has suddenly gone a bit weird about it all, asking questions like “Who will put up shelves for you, and who will cut the grass? I’ve pointed out that its not 1950 and that I can put up shelves and cut the grass but he’s still going on about it.

My partner knows there’s something upsetting me but I haven’t told him about my Dad’s comments yet. I’m not quite sure how to handle that conversation as he loves my folks. It’s really upsetting that my Dad is being off when it should be a happy time for us. Help please!

Ellen x

Our Answer

Hi Ellen,

Thanks for opening up about this scenario. I think it is more common than you may think, although that doesn’t make it feel any easier for you!
Being in a relationship with a disabled partner can indeed bring practical problems. But there are invariably solutions to most of them. Your parents naturally want their daughter to be looked after well but your Dad is focussing on what your partner can’t do!

The generations before us had their jobs clearly divided into ‘blue and pink’ jobs. Many of us now subscribe to that notion less and less. Perhaps your Dad’s perception is that to be the ‘man of the house’ you have to put up shelves and mow the lawn. This is how he felt he supported the family and looked after his girls. Doing these blue jobs validated him as a husband and father.

I wonder if it might be worth a chat with him about this way of thinking – as this isn’t necessarily dependent on your partners disability. You could have a non-disabled partner who is useless at putting up shelves!

I would also consider mentioning this to your Dad – what would happen if you married a non-disabled person and then they became a wheelchair user? You would naturally have to adapt to a new way of life as he may no longer be able to do these tasks. I doubt your Dad would encourage you to leave them because they can no longer mow a lawn.

It sounds like your Dad is a little fearful of the future and has gone into fatherly protective mode.
A simple, adult to adult chat to reassure him may be all he needs.

I think not getting angry or defensive will help you. It appears this is really coming from a place of concern from your Dad rather than a place of mean prejudice. A gentle talk, with confidence and assertion from yourself about how you will manage the household and the relationship as a whole, will allay his fears. It’s encouraging that he gets on well with your partner and has known him for a year. Your Dad will have seen the lovely attributes of your boyfriend; those you’ve fallen in love with. Hence why being in a relationship with a disabled partner doesn’t bother you, as it is about much more than practicalities of a disability.

It’s great that your partner really likes your parents, and I can understand why you may not want to disclose your Dad’s comments.  It could hurt your partner and emasculate him perhaps.  Or conversely, he may totally empathise with your Dad and be willing to talk to him to reassure him.  He may express how he contributes to the partnership and what that looks like to him.  His dedication, emotional support, commitment, love – all more important than him making Wimbledon-quality lawns!

And hey, if it’s such an issue, or your partner fancies mowing – he could always get hoisted up on to a ride-on one 😉

Good luck with the chats.  I have every confidence this can be easily sorted with a bit of empathy and compassion from both sides!

Zoe x

Stay Connected

Got a question for our Love Lounge team? Please contact us and we’ll do our best to help. Follow us on twitter and Instagram to keep up to date with all our goings on. Join our Undressing Disability Hub to learn more about sex and disability and to access free resources. #UndressingDisability #LoveLoungeUK

 

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A starry sky

My Vagina is The Star – Kiruna’s First Smear Test

By Disability, Undressing Disability

A guest blog by Kiruna Stamell.

I am a dwarf woman, a little person, person of restricted growth, person of short stature. That is my ‘thing’. Or the ‘thing’ people focus on.

As a result, I had this long-held belief that I had received my ‘lot’ in life. You know, I had my ‘thing’. I been served my life’s challenge. Somehow this made me arrogantly believe I was superior to getting cancer, herpes, murdered by a serial killer or being struck by lightning. I was simply too unique to be touched by common problems.

I am not alone as a disabled person in this thinking. It seems to be a common idea amongst us disabled folk and reinforced by non-disabled people that we already ‘carry our burden’. We are externally defined by our impairments so often, we too subconsciously internalise the belief, that our impairments are our [winces] ‘thing’.

So, a vaginal or cervical cancer thing was not on the list of things to worry about.

The ‘woman’ part of my identity felt flimsy, secondary to the desexualised label of ‘dwarf’, but she’s always been there. And one day, I woke up to the reality that my health isn’t just about my impairment.

I don’t know what happened, but I think it was a desire to feel like every other woman. All my average height and non-disabled friends were having their vaginas looked at and I wanted someone to look at mine.

Also, I had had a period refuse to stop and thought this was weird. So did my doctor.

My First Smear Test

The first challenge was that I was a virgin, and the doctors were funny about putting a speculum inside a virgin. I think, this is why I got sent to a proper gynaecologist straight away.

I was not so precious. I liked that my vagina was getting a lot of attention and being taken seriously. It took the medical focus off my height. All eyes were on my foof, and my foof was equalising!

At my first smear, lubricant was liberally applied. This was really helpful.

There were a couple of challenges:

  • The building was an old hospital, so door handles were too high for me to open, so I had to be escorted through the building.
  • Getting onto the bed was a challenge. Doing it gracefully and with no knickers on more so, as for me it was a literal climb. They made a step up onto it out of a chair and a smaller step stool.

I discovered that my cervix sits very high up and to the front. I’ve remembered this detail for all subsequent smears, telling the nurse saves so much time!

I find the weirdest bit is when the speculum parts. It feels a bit like when the dentist pulls your cheeks apart. Sometimes, my vagina creaks. Not audibly but like a sound you feel in your body. On a good cervical smear day, it just opens up and if to say ‘wow’. These occasions are rarer, and I only really remember that happening with the lube.

I find it reassuring getting a smear. I find it a really good reminder that being a ‘dwarf’ isn’t my only ‘thing’. I feel connected to humanity knowing I need to look after my sexual health as much as anyone else does.

When I am on that bed getting a smear, my vagina is the star. In that moment it is the most unique thing about me.

Cervical Screening Campaign

Learn more about our Cervical Cancer Red Tape campaign. which aims to remove the barriers that many disabled women face when accessing cervical screening and sexual health services. Search hashtag #CervicalScreeningRedTape to join the conversation and follow us on Instagram and Twitter.

We hope our tips for improving access to cervical screening make a difference. If you work in the healthcare sector please feel free to share them with your network.

 

Cervical Screening and Deaf Awareness

By Disability, Undressing Disability

Cervical screening saves lives and its so important that women have regular check-ups. So why did a survey by Jo’s Cervical Cancer Trust highlight that 88% of disabled women found accessing a smear test more difficult because of their impairment? Claire, our Deputy CEO shares her experience of cervical screening as a deaf woman.

6 Monthly Check Ups

A few years ago, I had to go for cervical screening tests every 6 months. It definitely wasn’t my favourite way to pass the time, but I know first-hand how essential it is. You see a smear test showed that I had moderate to severe abnormal cells caused by the HPV virus. Luckily for me it was picked up and I had laser therapy to destroy the abnormal cells. Now that’s resolved I go for a smear test every 3 years and hope for a positive experience. Unfortunately, a lack of deaf awareness frequently creates problems. As a result, I battle with feelings of anxiety before, during and after the test takes place. And I’m not alone. A study by Jo’s Cervical Cancer Trust found that 88% of disabled women found cervical screening tests difficult because of their impairments. Something needs to change!

My First Smear Test

The first time I had a smear test I didn’t really understand what was going on. I’m sure that’s common for many women but when you’re deaf there’s extra things to feel anxious about. For example, at my doctor’s surgery the examination room is right next to the busy waiting room. Before my smear test the nurse left the room for me to get undressed. She said she’d knock to make sure I was behind the cubicle curtain before coming back in. As I can’t hear the knock on the door, I felt panicked that I’d be exposed.

I explained that I was deaf, but unfortunately the nurse didn’t adapt her behaviour to ensure I was properly briefed. When preparing for the test she kept turning her head away to organise the equipment. This made it impossible to lipread, so I lay there with my anxiety growing by the second.

Once my knees were up and a sheet covering me, I couldn’t see what was about to happen. I knew she was talking to me, but I couldn’t hear what she was saying. I said “I can’t hear you” and instead of moving her head so I could lipread, she just stopped talking.

When she inserted the speculum there was no warning, so I tensed my body, and it was really painful. (I’m told by hearing friends that the nurse tells you when it’s about to be inserted and whilst it may be uncomfortable it usually doesn’t hurt.)

I also left the test with no idea of when to expect the results and went home upset and worried.

Deaf Awareness

My next experience of cervical screening was much more positive. The nurse told me her cousin was deaf, so she had great deaf awareness. Here’s what she did to make the smear test a much easier experience for me.

1. She explained the procedure from start to finish before asking me to get ready and lie on the bed.
2. Whilst explaining she maintained eye contact, used gestures, and demonstrated with the speculum what would happen. When I didn’t understand one part, she got a pen and paper and wrote it down.
3. When leaving the room for me to get undressed she said she’d be back in 5 minutes, rather than saying ‘she’d knock’. I looked at the time on my phone, got ready and waited.
4. We agreed that she would tap my leg as a sign that she was about to insert the speculum, giving me a moment to relax and prepare.
5. She understood that I was very anxious because of my previous experience and reassured me.

Make Appointments, Not Assumptions

If you are deaf and have never had a smear test, then please don’t be put off by my initial experience. Cervical Screening saves lives. My aim of sharing such a personal insight is that it will help bring about change, and help the disabled community have equal access to the services others access easily.

For medical professionals reading this hopefully my tips will be useful and improve deaf awareness within your surgery or clinic. Find more insight on our campaign page. 
#CervicalScreeningRedTape

Follow Our Campaign

Read more about our #CervicalScreeningRedTape campaign and follow us on twitter @ETUKUndressing and Instagram @UndressingDisability.

 

Worried about Cervical Screening?

Visit the Jo’s Cervical Cancer Trust website where you’ll find lots of practical information, advice and a forum where you can pose questions and share experiences.

#CervicalScreeningRedTape campaign

By Disability, Undressing Disability

Our #CervicalScreeningRedTape campaign aims to highlight the fact that many disabled women are finding it difficult to access cervical screening.

The Issues

Common barriers to accessing cervical screening are:

  • Disabled women not being offered a smear test as it is often assumed that they are not sexually active and are less likely to need a test.
  • Physical barriers such as a lack of non-adjustable beds in GP surgeries.
  • Fear. Due to a previously negative experience. Or a self-consciousness as their body may differ to what they believe medical staff are used to seeing.
  • Expense. Often disabled women have to travel further than their local surgery to attend an accessible clinic.

Potential Solutions

What can be done to improve access to smear tests for disabled women? Below are four potential solutions.

  1. Recognise that disabled adults can enjoy an active sex life and offer as standard cervical screening and sexual health tests.
  2. Ask what an individual’s needs are. If your surgery does not have accessible facilities that meet the needs of a disabled patient, then have a procedure in place where you can offer an alternative location. This saves both you and the disabled woman a lot of time and effort phoning around. Read Emily’s blog for a real-life example. 
  3. Realise that standard procedures won’t work for everyone. For example, due to physicality it may be easier for a woman to have a smear lying on her side rather than on her back. We are all different, and often know our bodies well. So if it’s feasible to do things differently, be willing to give it a try.
  4. Most women are apprehensive about having a smear test but for many disabled women there is an extra layer of nervousness. Reassurance prior to the test being booked can help alleviate this fear.

We fully appreciate the challenges our NHS is facing during the pandemic and know that wait times may be longer than usual, however we hope our solutions can become best practice.

Useful Resources

Undressing Disability Podcast

Dr Larisa Corda OBGYN and presenter Sam Renke are guests on Episode 2 of our Undressing Disability podcast. Joined by our CEO Jennie Williams they share personal experiences of the issues around accessing cervical screening raised in this #CervicalScreeningRedTape campaign.

 

Blog

Emily wrote about her experience as a wheelchair user of trying to access her first ever smear test in this blog article.

The Undressing Disability Hub

Last year we launched our Undressing Disability Hub which is free to join. It is full of free resources on topics relating to sex and disability. Members include professionals working in the fields of medicine, psychology, and care homes. As well as sex educators and those searching for a safe network to learn and share information on the topic of sex and disability.

Sign up for free today.

Worried about Cervical Screening?

Jo’s Cervical Cancer Trust is a charity which provides information and support on the topic of cervical cancer. Their website https://www.jostrust.org.uk/ is full of valuable insight and they do an incredible job raising awareness and saving lives with their work.

#CervicalScreeningRedTape 

Stay Up To Date

Follow our campaign on social media on twitter @ETUKUndressing and Instagram @UndressingDisability. #CervicalScreeningRedTape

 

Bedroom Adventures Logo is a black lacy eye mask with the brand name in curvy black writing below

Win A Decor Heart Wedge From Bedroom Adventures

By Disability, Undressing Disability

This competition is now closed. Congratulations to winner Rosie Glen.

A graphic of a crown with the word WINNER written on it and the name Rosie Glen below. The background is bright blue

It’s competition time!

Thanks to Bedroom Adventures we have a Décor Heart Wedge to give away to one lucky winner. Perfectly contoured for the derriere, the Décor Heart Wedge provides a sweet incline for deeper penetration and G-spot positioning during lovemaking. This compact version of the Wedge combines passion with fashion as a positioning aid that doubles as a decorative pillow.

A merlot red coloured heart shaped cushion

Prize:

1 x The Décor Wedge, gifted by Bedroom Adventures.

How to Enter:

Simply sign up to the Undressing Disability hub, complete your profile and a profile photo and you’ll automatically be entered.

Competition Ends:

Thursday 26th November at 12 noon

Winner Announced:

Tuesday 1st December at 12 noon.

Terms & Conditions: All new and existing hub members who have completed a profile, including uploading an image as a profile picture, will be entered into the competition. The winner will be contacted by email and also messaged on the hub. The winner must respond within 24 hours to confirm they wish to receive the prize, if not a new winner will be selected. Your prize will then be posted directly to you.

A lady in black basque and knickers poses on a bed holding the heart wedge

More Product Details

  • Compact version of the Wedge provides lift and angles for deeper penetration.
  • Perfectly contoured for the derriere.
  • Ultra soft velvish material in designer colours to match your bedding.
  • Removable, machine-washable cover.
  • Moisture-proof liner prevents moisture from penetrating the foam interior.
  • Measurement in inches: 18L x 14W x 7H

Bedroom Adventures

Thank you to Bedroom Adventures for the generous gift of this prize. Damian, owner of Bedroom Adventures is one of our Love Lounge sexperts, offering practical advice on getting the most from your sexual relationships. If we can help solve a dating dilemma or relationship question contact us in confidence.

Follow our Undressing Disability campaign on social media. Find us on Instagram and twitter, or search hashtag #UndressingDisability.

 

hanging rack with shirts on hangers

Styling It Out and Sweaty Pits

By Disability, The Love Lounge

The Question

Hi,

Two things I need your advice on, styling it out and sweaty pits! One is fashion, the second is  less sexy. I’ve been single for ages, focusing on my studies and getting a job following a time of ill health. In the last eighteen months I’ve managed to lose the extra weight I had piled on after surgery.

I’m feeling confident about myself but have zero clue when it comes to clothes. I’ve either got work shirts or hoodies and want to look trendier than that. I see blokes with a bit of style and think they look cool but I’ve no idea how to put clothes together.

The more personal issue is that sometimes I get wet patches on my shirt when I’m having a sweaty day. I think it’s a side effect of medication I’m taking. I’m embarrassed by it. I prefer to layer clothes on my top half to avoid people noticing. And I’m going to see if there’s a stronger deodorant I can use as I don’t want sweaty pits when I’m dating.

Any tips on where I can look for style advice. My mates are as clueless as me.

Cheers.

Our Answer

Hi! Thanks so much for writing in to the Love Lounge.

It’s great that you’re feeling confident. That’s more than half the battle when it comes to fashion! I’d recommend going into a department store, like Topshop or River Island and taking advantage of their Personal Styling Service. It’s usually free and involves a staff member who specialises in styling going around the store with you. They’ll pick out clothes that suit your new body type, complement your skin tone and make you feel great. It’s a brilliant thing to experience as it’ll then provide you with tips to use when you go out shopping on your own. If that’s not for you then search YouTube for videos with titles like ‘BooHoo Try On Haul’ where the fashionistas suggest how to put outfits together.

A bit of advice. Don’t worry too much about what’s in fashion and what others are wearing. Instead, use that energy to focus on what makes you feel amazing inside. Good clothes have the ability to boost your mood internally, too.

Styling It Out and Sweaty Pits - a trendy young guy wears a burgundy velvet suit jacket with a patterned T-shirt underneath. He has a hipster beard, a man bun and sunglasses

Sweaty Pits

Regarding the wet patches, I’d recommend discussing this with your doctor. They may be able to change your medication to minimise this side effect. Layering clothes, experimenting with deodorants and even doing a bit of research on what colours and materials work best with sweat patches will all go some way in helping you feel comfortable. However hopefully there is a more permanent solution!

Wishing you all the best – you’ll be as stylish as can be in no time!
Em x

Send Us Your Questions

Can our team help with a dating dilemma, sex or relationship question? Get in touch and we’ll do our utmost to find the answers you need. Follow us on Instagram @UndressingDisability and twitter @ETUKUndressing.
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Worried About My Boyfriend's Behaviour - a woman sits leaning against the back of the sofa looking sad, her boyfriend wears a blue and white checked shirt, has dark hair and a beard and stares into the distance looking grumpy

Worried About My Boyfriend’s Behaviour

By Disability, The Love Lounge

The Question

Dear Love Lounge,

I’m worried about my boyfriend’s behaviour. We met about 4 months ago and things have moved fast. We are crazy about each other and he has moved in. At first it was all very romantic, and he made me feel great. He complimented my appearance and was kind and generous and loving. My family are happy that I’ve met someone but wanted me to wait a while longer before he moved in, worrying I might get hurt as this is my first relationship. I dismissed their concerns as I’m 27 and wish they’d stop babying me. My mum was my carer until I got a PA and my own flat a few years ago, and she can forget I’m not a kid anymore.

In the last few weeks, my boyfriend has been short tempered and a lot less affectionate. Little things about me seem to annoy him. When we’re with friends and family he is fine but when we’re alone he frequently makes comments about my weight and has told me that I’m ‘stupid’ and ‘dense.’ I think he might also have used my bank card as it went missing from my wallet then reappeared. I have cried about this which made him more annoyed so I’m nervous of talking to him about his mood in case I make it worse. I know that couples can ‘have their moments’ as my sister so it may just be the norm?

Advice welcome.

 

Our Answer

Hi there, and thanks so much for writing in to us.

First things first, anything that makes you feel this upset and unhappy isn’t the norm.  Couples absolutely ‘have their moments’ but you are right to be worried about your boyfriend’s behaviour change. He is being neither kind nor respectful to you by the sounds of it, and this behaviour should not be accepted.

It’s good to hear that everything was great at the beginning. Has anything changed dramatically for your partner since then? Big changes at work, with money or even with family and friends can have a major impact on how we behave. And whilst it doesn’t make what he’s doing right, it might explain the reasoning behind his behaviour.

It is worrying that your boyfriend is only acting this way when you’re alone. This suggests to me that he knows the way he is acting is not acceptable.

Communication is key here. You must let him know plainly and simply (without getting too emotional if you can) that you won’t stand for comments from him that are demeaning or degrading. You won’t accept comments that make you feel bad about yourself – no-one deserves that in a relationship.

At the same time, let him know that if there is anything going on for him that you can help with, you’d be more than happy to. And if you can’t help, you’ll support him to sort it out himself. Remind him that you love him and of how great everything was at the beginning. But to get back to that, he must change his ways and how he treats you.

Tread carefully regarding the bank card – he might have genuinely picked yours up by mistake – and if no money has left your account, it seems unnecessary to accuse him of stealing. Have a chat with him about everything. How he reacts will probably tell you all you need to know about the future of your relationship.

Good luck!
Em x

 

Send Us Your Questions

Can our team help with a dating dilemma, sex or relationship question? Get in touch and we’ll do our utmost to find the answers you need. Follow us on Instagram @UndressingDisability and twitter @ETUKUndressing.

 

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Grip Issues - How To Spice Up Your Sex Life - A dark haired woman leans forward to touch her male partner, he kisses her forehead. She is laughing and there is a window in the background

Grip Issues – How To Spice Up Your Sex Life

By Disability

I’m hoping to spice up my sex life with my boyfriend.  We’ve been together for 3 years and things have started to become a bit same-y in the bedroom. Have you got any recommendations of toys or equipment we could use? We’re open to anything, but my cerebral palsy means I struggle with grip, and going on top takes a fair bit of time and effort!

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