FabSwingers.com > Forums > The Lounge > Calling all fabbers with disabilities
Calling all fabbers with disabilities
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By (user no longer on site) OP
over a year ago
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Just wondering if there’s anyone else like me who’s got either a hidden or visible disability of any degree? You don’t need to share what if you don’t need to.
Be interesting to hear how you manage a good sex life and what adaptations you may or may not need.
I have chronic pain (fibromyalgia) and ME/CFS and some other stuff (won’t go into it) so although not visible I’m knackered lol. Day to day varies but when I do too much I’m screwed literally and metaphorically lol. X
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By (user no longer on site) OP
over a year ago
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"Well I wasn't expecting to see a thread like this.. yes I have fibromyalgia and arthrytis. Mrs B.
 "
It’s important to be talked about and accepted. Disabled people/sick people have sex too lol.
Sorry to hear that. Pain sucks! Always here to chat or bitch too as someone who “gets it”. X |
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By (user no longer on site)
over a year ago
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"Well I wasn't expecting to see a thread like this.. yes I have fibromyalgia and arthrytis. Mrs B.
It’s important to be talked about and accepted. Disabled people/sick people have sex too lol.
Sorry to hear that. Pain sucks! Always here to chat or bitch too as someone who “gets it”. X"
Yep, CFS/ME, have Fibro markers too. I'm still stupidly strong but get tired pretty quickly and suffer for days. Shame that more medical professionals don't recognise it appropriately, worst thing is there are likely to be many more that don't fully recover post Covid.  |
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By (user no longer on site)
over a year ago
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"Just wondering if there’s anyone else like me who’s got either a hidden or visible disability of any degree? You don’t need to share what if you don’t need to.
Be interesting to hear how you manage a good sex life and what adaptations you may or may not need.
I have chronic pain (fibromyalgia) and ME/CFS and some other stuff (won’t go into it) so although not visible I’m knackered lol. Day to day varies but when I do too much I’m screwed literally and metaphorically lol. X
"
I don't look at it as a disability cos I'm at a rehabilitative stage of an extremely severe brain infection - so I get tired very easily. |
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I don't tend think of myself as having disabilities.
However, I wear hearing aids and have balance problems related to the hearing loss.
Rarely causes any issues but hot tubs or pools in clubs are generally a no no. |
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By (user no longer on site) OP
over a year ago
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"Just wondering if there’s anyone else like me who’s got either a hidden or visible disability of any degree? You don’t need to share what if you don’t need to.
Be interesting to hear how you manage a good sex life and what adaptations you may or may not need.
I have chronic pain (fibromyalgia) and ME/CFS and some other stuff (won’t go into it) so although not visible I’m knackered lol. Day to day varies but when I do too much I’m screwed literally and metaphorically lol. X
I don't look at it as a disability cos I'm at a rehabilitative stage of an extremely severe brain infection - so I get tired very easily. "
I had viral meningitis which was what kicked off my ME. Initially they called it post viral fatigue but because I didn’t recover at all they did some more digging and diagnosed the ME.
Take care. Rest up and pace xx |
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By (user no longer on site) OP
over a year ago
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"Hidden disability here.
I rarely let it get in the way of a very active life.
I'll wait until I really am unable to do anything to give up. "
I try to but some days are harder than others. Great attitude though xx |
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By (user no longer on site) OP
over a year ago
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"I don't tend think of myself as having disabilities.
However, I wear hearing aids and have balance problems related to the hearing loss.
Rarely causes any issues but hot tubs or pools in clubs are generally a no no."
Thank you for sharing. Yes water and ear infections and hearing impairments are difficult my first girlfriend was hearing impaired. She had hearing aids and lip reads. X |
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By (user no longer on site) OP
over a year ago
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"I have invisible disabilities. Generally not a sex life issue. Occasionally comes up. Generally just need people willing to work with me. I've got a lot of work arounds"
For me it can interfere with a long term partner more I suppose. It’s the whole not being able to do certain positions or being in pain after or exhausted etc. One night stands I tend to suck it up (not that I have many!). I’ve had shoulder surgery so if I’m being restrained in anyway I have to be careful etc. Like you say you find a way to work around it. Xx |
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By (user no longer on site) OP
over a year ago
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"Well I wasn't expecting to see a thread like this.. yes I have fibromyalgia and arthrytis. Mrs B.
It’s important to be talked about and accepted. Disabled people/sick people have sex too lol.
Sorry to hear that. Pain sucks! Always here to chat or bitch too as someone who “gets it”. X
Yep, CFS/ME, have Fibro markers too. I'm still stupidly strong but get tired pretty quickly and suffer for days. Shame that more medical professionals don't recognise it appropriately, worst thing is there are likely to be many more that don't fully recover post Covid. "
I’m on loads of online support groups and we are inundated of post viral fatigue cases following Covid but they are very different to fibro and ME.
Sorry to hear that. Get an appointment with A good rheumatologist having the diagnosis on paper helps xx |
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By (user no longer on site)
over a year ago
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Partner suffers with Fibro. Suffers daily, especially if she had a active day before such as lots of walking etc.
Certain food triggers/makes it worse. Such as caffeine, and taking naps also makes her bad.
Sex life is amazing, just sometimes she can't do everything she wants, such as being on top etc.
Just need to find someone understanding and note down what the triggers are, if there are any. I know Fibro has a a spectrum of severity, so some has triggers some doesn't I guess?
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A heart condition and chronic pain from endometriosis. Also fucking knackered all the time or lay with my legs up the back of the sofa trying to ease the aching.
I manage my sex life by being aware of how I can enjoy sex and communicating with my sexual partners. I'm lucky to have people who work with me to make it great for us both. Also bonus points if they'll rub my sore calves and ankles when my pain flares up. My partner says I make sex noises when he does it  . |
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"I don't tend think of myself as having disabilities.
However, I wear hearing aids and have balance problems related to the hearing loss.
Rarely causes any issues but hot tubs or pools in clubs are generally a no no.
Thank you for sharing. Yes water and ear infections and hearing impairments are difficult my first girlfriend was hearing impaired. She had hearing aids and lip reads. X"
There's lots of people with hidden disabilities.
I know many are unaware of mine, as I wear hidden aids and manage the dizziness well most of the time.
I hope it helps people to be more understanding and supportive of those with disabilities, especially less obvious ones. |
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By (user no longer on site)
over a year ago
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Hypermobility, severe.
Means I cannot stand or walk for long periods and getting on top is short bursts.
I am fine most the time during, but will suffer after.
Also makes me exhausted alot of the time. |
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Me! I became disabled after my last pregnancy, due to pelvic and peripheral nerve injury caused by the growing baby plus a severely prolapsed disc (with massive nerve root compression). I use a wheelchair now for anything other than walking to/from the car because it reduces my pain and means I can go as far as I'd like. I spent nearly 3 years trying to cope on crutches but realised the chair would give me my freedom back. I play wheelchair sports, go out on medium/long pushes with a running club (5-10k and a bit more) and take nerve modulating drugs for my pain.
Sex wise, doesn't affect me much. I can't do standing or squatting but that's about it. I do have reduced sensation but still enjoy sex and cum with someone who knows what they're doing and is patient  |
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By (user no longer on site)
over a year ago
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chronic pain (after breaking my back), severe hypermobility, degenerative kidney disease, split pelvis ... amongst a whole host of severe MH issues.. And whatever else i've forgotten.
proper catch aren't i 
try not to let it affect things too badly.. but there's things i just can't do.. Or can only do for a little while.. and either way, I'll be in clip for days afterwards!
nice to know we aren't alone, thanks OP!
Px  |
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By (user no longer on site) OP
over a year ago
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"A heart condition and chronic pain from endometriosis. Also fucking knackered all the time or lay with my legs up the back of the sofa trying to ease the aching.
I manage my sex life by being aware of how I can enjoy sex and communicating with my sexual partners. I'm lucky to have people who work with me to make it great for us both. Also bonus points if they'll rub my sore calves and ankles when my pain flares up. My partner says I make sex noises when he does it . "
Hey I’m a fellow endo warrior too it’s up there as one of the most painful conditions. I feel ya. Got my pre op appointment for my first lap soon xx |
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By (user no longer on site) OP
over a year ago
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"I don't tend think of myself as having disabilities.
However, I wear hearing aids and have balance problems related to the hearing loss.
Rarely causes any issues but hot tubs or pools in clubs are generally a no no.
Thank you for sharing. Yes water and ear infections and hearing impairments are difficult my first girlfriend was hearing impaired. She had hearing aids and lip reads. X
There's lots of people with hidden disabilities.
I know many are unaware of mine, as I wear hidden aids and manage the dizziness well most of the time.
I hope it helps people to be more understanding and supportive of those with disabilities, especially less obvious ones. "
This was my aim by raising awareness xx |
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By (user no longer on site) OP
over a year ago
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"Hypermobility, severe.
Means I cannot stand or walk for long periods and getting on top is short bursts.
I am fine most the time during, but will suffer after.
Also makes me exhausted alot of the time."
Oh hypermobilty is brutal is yours EDS ? X |
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By (user no longer on site) OP
over a year ago
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"chronic pain (after breaking my back), severe hypermobility, degenerative kidney disease, split pelvis ... amongst a whole host of severe MH issues.. And whatever else i've forgotten.
proper catch aren't i
try not to let it affect things too badly.. but there's things i just can't do.. Or can only do for a little while.. and either way, I'll be in clip for days afterwards!
nice to know we aren't alone, thanks OP!
Px "
Oh I feel ya. I didn’t put my list coz it scares even me. I live with a diagnosis of BPD. It’s all fun and games. Life’s sent to challenge ya hey.
Mental health is also important to talk about.
Again always here as someone who gets it xx |
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By (user no longer on site) OP
over a year ago
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Thank you everyone for all your participation. It’s amazing what people go through and how much we endure.
Always here if anyone wants a chat to someone who gets it.
X |
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I have arthritis and nerve damage in my knees and legs . Started off after stepping on a piece of lego and twisting my leg to get off it x
The only part of my sex life that suffers is I can't get on top. My knees just won't allow it |
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"A heart condition and chronic pain from endometriosis. Also fucking knackered all the time or lay with my legs up the back of the sofa trying to ease the aching.
I manage my sex life by being aware of how I can enjoy sex and communicating with my sexual partners. I'm lucky to have people who work with me to make it great for us both. Also bonus points if they'll rub my sore calves and ankles when my pain flares up. My partner says I make sex noises when he does it .
Hey I’m a fellow endo warrior too it’s up there as one of the most painful conditions. I feel ya. Got my pre op appointment for my first lap soon xx"
Best of luck for it! |
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By (user no longer on site) OP
over a year ago
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"I have arthritis and nerve damage in my knees and legs . Started off after stepping on a piece of lego and twisting my leg to get off it x
The only part of my sex life that suffers is I can't get on top. My knees just won't allow it "
Oh bless you. Arthritis is painful enough though x |
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By (user no longer on site) OP
over a year ago
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"A heart condition and chronic pain from endometriosis. Also fucking knackered all the time or lay with my legs up the back of the sofa trying to ease the aching.
I manage my sex life by being aware of how I can enjoy sex and communicating with my sexual partners. I'm lucky to have people who work with me to make it great for us both. Also bonus points if they'll rub my sore calves and ankles when my pain flares up. My partner says I make sex noises when he does it .
Hey I’m a fellow endo warrior too it’s up there as one of the most painful conditions. I feel ya. Got my pre op appointment for my first lap soon xx
Best of luck for it! "
Thank you  |
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By (user no longer on site)
over a year ago
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"Hypermobility, severe.
Means I cannot stand or walk for long periods and getting on top is short bursts.
I am fine most the time during, but will suffer after.
Also makes me exhausted alot of the time.
Oh hypermobilty is brutal is yours EDS ? X"
I believe so but not diagnosed. I show alot of the symptoms though.
Espescially the easily bruising, cant even poke me! Lol |
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By (user no longer on site)
over a year ago
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Absolouetly shocking bad back. Sometimes I cant do the most simple things in life like walking. Hoovering up. Hanging washing up and I even lean over the sink to wash the pots. |
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By (user no longer on site)
over a year ago
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I also have fibro - it affects me every day, there just aren't enough pain killers in the world.
Fab has given me one area of my life which isn't affected by my fibro - my social life has taken a massive hit because of my fatigue - but with fab I can enjoy sex on my terms, and actually the endorphins definitely help my pain, and helps me forget it for a few hours at least. I will hide my profile when I'm feeling particularly poorly.
Great post, it makes me feel a little bit less alone with this xx |
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By (user no longer on site) OP
over a year ago
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"Absolouetly shocking bad back. Sometimes I cant do the most simple things in life like walking. Hoovering up. Hanging washing up and I even lean over the sink to wash the pots. "
I feel ya. Being busty doesn’t help either does it x |
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By (user no longer on site) OP
over a year ago
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"I also have fibro - it affects me every day, there just aren't enough pain killers in the world.
Fab has given me one area of my life which isn't affected by my fibro - my social life has taken a massive hit because of my fatigue - but with fab I can enjoy sex on my terms, and actually the endorphins definitely help my pain, and helps me forget it for a few hours at least. I will hide my profile when I'm feeling particularly poorly.
Great post, it makes me feel a little bit less alone with this xx"
All in this together. As I’ve said to others always here to have a chat if you need it xx |
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By (user no longer on site) OP
over a year ago
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"between us we have loads Arri has fibrro, i have epelepsy and arthritis, among other things, but drugs keep us prety much on the go xx"
Yay for drugs lol (legal ones) x |
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By (user no longer on site)
over a year ago
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I have dyspraxia which is defined as a disability, but I've never considered it a disability. Makes some every day tasks difficult but I can tackle those or find a way to work through them. It's just a part of me. |
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By (user no longer on site) OP
over a year ago
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"I have dyspraxia which is defined as a disability, but I've never considered it a disability. Makes some every day tasks difficult but I can tackle those or find a way to work through them. It's just a part of me."
I totally get it. That’s a positive attitude xx |
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By *erces LetiferMan
over a year ago
Somewhere off the edge of the map... 'ere there be monsters |
"The wife has fibromyalgia and hypermobility. It effects our social life as well as our sex life.
. I’m sorry to hear that. Xx"
Thanks. Just makes you realise life’s for living and we should all have as much fun and pleasure as we possibly can. x |
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By (user no longer on site) OP
over a year ago
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"The wife has fibromyalgia and hypermobility. It effects our social life as well as our sex life.
. I’m sorry to hear that. Xx
Thanks. Just makes you realise life’s for living and we should all have as much fun and pleasure as we possibly can. x"
A fucking men. I totally agree hence me being here before my health gets too bad. X |
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I have Aspergers. It doesn't tend to effect my/our sex life.
The only real issue is that I can get fixated on something (e.g. an upcoming meet, new toy coming in the post, etc.). On those occasions, Alice needs to give me a loving slap and kinda bring me out of it.
I like being slapped, so it's a win-win! |
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By (user no longer on site) OP
over a year ago
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"I have Aspergers. It doesn't tend to effect my/our sex life.
The only real issue is that I can get fixated on something (e.g. an upcoming meet, new toy coming in the post, etc.). On those occasions, Alice needs to give me a loving slap and kinda bring me out of it.
I like being slapped, so it's a win-win! "
Ahhh fixation it’s really common with ASC.
Haha I don’t slap my clients but a gentle reminder or change of focus works just as well haha.
 |
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"I have SSD from the chronic pain of a spinal injury, PTSD, all from military service. I still enjoy sex, but now it takes me a long time to cum!"
I know how you feel with the long time to cum thing. Same boat here with nerve damage |
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I've suffered with psioratic arthritis for the last 7 years, and currently have a gout flare up in ma hand/wrist. It can be paiful at times, buy I know there are plenty of people in much worse position than me  |
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By (user no longer on site)
over a year ago
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"Just wondering if there’s anyone else like me who’s got either a hidden or visible disability of any degree? You don’t need to share what if you don’t need to.
Be interesting to hear how you manage a good sex life and what adaptations you may or may not need.
I have chronic pain (fibromyalgia) and ME/CFS and some other stuff (won’t go into it) so although not visible I’m knackered lol. Day to day varies but when I do too much I’m screwed literally and metaphorically lol. X
I don't look at it as a disability cos I'm at a rehabilitative stage of an extremely severe brain infection - so I get tired very easily.
I had viral meningitis which was what kicked off my ME. Initially they called it post viral fatigue but because I didn’t recover at all they did some more digging and diagnosed the ME.
Take care. Rest up and pace xx"
Thank you - meningitis and encephalitis here. I can sleep for England. |
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By (user no longer on site)
over a year ago
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"I don't tend think of myself as having disabilities.
However, I wear hearing aids and have balance problems related to the hearing loss.
Rarely causes any issues but hot tubs or pools in clubs are generally a no no.
Thank you for sharing. Yes water and ear infections and hearing impairments are difficult my first girlfriend was hearing impaired. She had hearing aids and lip reads. X
There's lots of people with hidden disabilities.
I know many are unaware of mine, as I wear hidden aids and manage the dizziness well most of the time.
I hope it helps people to be more understanding and supportive of those with disabilities, especially less obvious ones.
This was my aim by raising awareness xx"
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By (user no longer on site)
over a year ago
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"Absolouetly shocking bad back. Sometimes I cant do the most simple things in life like walking. Hoovering up. Hanging washing up and I even lean over the sink to wash the pots.
I feel ya. Being busty doesn’t help either does it x"
no it doesnt help at all. I keep saying to hubby he needs something with weights on his chest everyday and see how it pulls him forward. I've lost an inch of my height lol. Not the best place to lose it  |
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By (user no longer on site)
over a year ago
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"I've suffered with psioratic arthritis for the last 7 years, and currently have a gout flare up in ma hand/wrist. It can be paiful at times, buy I know there are plenty of people in much worse position than me "
pains pain regardless of the cause  |
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By (user no longer on site) OP
over a year ago
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"Ahhh fixation it’s really common with ASC.
Haha I don’t slap my clients but a gentle reminder or change of focus works just as well haha.
Thanks for using a C instead of a D."
I find the term disorder really offensive. It’s a not a disorder it’s the way people with autism are wonderfully wired and unique so prefer the term condition. |
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By (user no longer on site) OP
over a year ago
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"Absolouetly shocking bad back. Sometimes I cant do the most simple things in life like walking. Hoovering up. Hanging washing up and I even lean over the sink to wash the pots.
I feel ya. Being busty doesn’t help either does it x no it doesnt help at all. I keep saying to hubby he needs something with weights on his chest everyday and see how it pulls him forward. I've lost an inch of my height lol. Not the best place to lose it "
Chiropractor has really really helped me x |
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"Autism.
Doesn't affect sex badly (quite the opposite in fact!) but socials are a major challenge.
We empathise "
Thanks. I never tell people before a meet because most people have a preconceived idea of what an autistic person is like.
I'm not shy, I'm quiet. There's a difference.
Also 'signals' like body language, facial expressions and tone of voice are completely lost on me.
I can't perceive them at all. |
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"Autism.
Doesn't affect sex badly (quite the opposite in fact!) but socials are a major challenge.
We empathise
Thanks. I never tell people before a meet because most people have a preconceived idea of what an autistic person is like.
I'm not shy, I'm quiet. There's a difference.
Also 'signals' like body language, facial expressions and tone of voice are completely lost on me.
I can't perceive them at all."
Again, without giving away secrets, we totally get it |
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By (user no longer on site) OP
over a year ago
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"IBD. Not great to chat about
I'm well most of the time, doesn't affect my day to day unless I'm having a flare up. "
IBD is nasty though I have IBS and that’s bad enough. Bless you xx |
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By *eesideMan
over a year ago
margate sumwear by the sea |
"Hi.
I have hidden disabilitys.
I'm dyslexic and asparagus.
Same as me but I hide them well.
T"
I did that to but it only made them wors.
Especially my asparagus.
Now I stopped hideing them and both more my asparagus than dyslexia have gotten a lot better.
Thow my spelling is mostly better down to Alto spell software. |
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Yep, hidden ones here. The people who need to know about them are told and we work around them I tend to keep them quite well hidden in day to day life, I dont like alot of fuss  alot of people close to me dont know. |
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By (user no longer on site) OP
over a year ago
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"Yep, hidden ones here. The people who need to know about them are told and we work around them I tend to keep them quite well hidden in day to day life, I dont like alot of fuss alot of people close to me dont know. "
Oh bless you I have only just accepted mine so trying to talk about it more x |
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Severe migrains, high blood pressure, and metal knees . I take candestaten with makes my bones ache which inturn makes my knees hurt more than they already do. If been accident prone was a disability that too lol |
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By (user no longer on site) OP
over a year ago
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"Severe migrains, high blood pressure, and metal knees . I take candestaten with makes my bones ache which inturn makes my knees hurt more than they already do. If been accident prone was a disability that too lol"
Ouch all sounds like fun and games. Amitryptaline helps with migraines but makes you quite sleepy so might not help the clumsiness. Swings and roundabouts hey! |
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By (user no longer on site)
over a year ago
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I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with  |
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By (user no longer on site)
over a year ago
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Had tickets to see Lady Ga Ga at the O2 a couple of years back and she had to cancel because of this. Still waiting for her to visit the UK.
Best wishes,
Adam x |
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By (user no longer on site) OP
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with "
You manage really well with it though I wouldn’t have known on my other posts. It’s a struggle. There’s a few others who are on the spectrum here |
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By (user no longer on site) OP
over a year ago
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"Had tickets to see Lady Ga Ga at the O2 a couple of years back and she had to cancel because of this. Still waiting for her to visit the UK.
Best wishes,
Adam x"
Yep lady G is very open about her struggle with Fibro. She collapsed with pain and fatigue bless her. X |
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with
You manage really well with it though I wouldn’t have known on my other posts. It’s a struggle. There’s a few others who are on the spectrum here "
Yeah I do well to hide it , mind if people know what to look for they usually ask me if I am , which I'm happy to answer and talk about , but yeah as you say youd not really know until I tell people , but yeah I struggle to make friends and maintain relationships but I'm really trying hard to make new friends and maintain regular chatting |
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By (user no longer on site)
over a year ago
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I have schizophrenia, anxiety and depression
seen someone mention Raynauds as well
I got that in my finger once
it went black and and i lost the feeling in my finger
thankfully it came back though
still won a pro evo tourney on the playstation with it |
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with "
I'm exactly the same.
I'm also like a dog with a bone sometimes and just can't leave things that I probably should.
|
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with
I'm exactly the same.
I'm also like a dog with a bone sometimes and just can't leave things that I probably should.
"
Thats me all over , sometimes its just extremely hard to let things go isn't it |
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with
I'm exactly the same.
I'm also like a dog with a bone sometimes and just can't leave things that I probably should.
Thats me all over , sometimes its just extremely hard to let things go isn't it "
Impossible at times and its got me into trouble a fair bit. |
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with
I'm exactly the same.
I'm also like a dog with a bone sometimes and just can't leave things that I probably should.
Thats me all over , sometimes its just extremely hard to let things go isn't it
Impossible at times and its got me into trouble a fair bit."
Oh I can imagine , I often get told I need to relax and let things go , but sometimes I can lose sleep if something is constantly on my mind |
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What a great post I’m a carer and look after people with disability’s.
Won’t mention My dodgy hip, bad knees curvature oF spine !!
I hope it’s a better world and most people are nice and more caring |
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By (user no longer on site)
over a year ago
|
"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with
I'm exactly the same.
I'm also like a dog with a bone sometimes and just can't leave things that I probably should.
Thats me all over , sometimes its just extremely hard to let things go isn't it
Impossible at times and its got me into trouble a fair bit.
Oh I can imagine , I often get told I need to relax and let things go , but sometimes I can lose sleep if something is constantly on my mind "
Yes it really isn't that simple.
You know you should just "let it go" but you just cant x |
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By (user no longer on site) OP
over a year ago
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"What a great post I’m a carer and look after people with disability’s.
Won’t mention My dodgy hip, bad knees curvature oF spine !!
I hope it’s a better world and most people are nice and more caring "
I’m also a carer but starting to think I’m the one who needs one x |
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with
I'm exactly the same.
I'm also like a dog with a bone sometimes and just can't leave things that I probably should.
Thats me all over , sometimes its just extremely hard to let things go isn't it
Impossible at times and its got me into trouble a fair bit.
Oh I can imagine , I often get told I need to relax and let things go , but sometimes I can lose sleep if something is constantly on my mind
Yes it really isn't that simple.
You know you should just "let it go" but you just cant x"
Yeah exactly , like then if its stuck in my head if I can not resolve it as quick as possible I end up over thinking about things and getting worse x |
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By *mmmMaybeCouple
over a year ago
West Wales |
"What a great post I’m a carer and look after people with disability’s.
Won’t mention My dodgy hip, bad knees curvature oF spine !!
I hope it’s a better world and most people are nice and more caring
I’m also a carer but starting to think I’m the one who needs one x"
H was in the industry for fifteen years until the Dr was fed up with her bad back, sent her off for an MRI & it turned out that at 36yrs old she has degenerative disc disease & Fibro amongst the other stuff she was already dealing with.
We thought the back was just the job & asked if they could fuse the lower vertebrae but it's every disc in her back! it's an hereditary thing & there's nothing to be done except pain relief. She's now walking with a stick at 40 :-/
S |
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"I would call it more health conditions than disabilities but I have asthma, IBS, gluten allergy, severe hormonal migraines, and chronic fatigue. Other than that I’m all good. "
Have you ever found anything to help with hormonal migraines,they are nasty |
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By *ouanna JoWoman
over a year ago
A little village |
"I would call it more health conditions than disabilities but I have asthma, IBS, gluten allergy, severe hormonal migraines, and chronic fatigue. Other than that I’m all good.
Have you ever found anything to help with hormonal migraines,they are nasty "
They are absolutely dreadful aren’t they
Sumatriptan on prescription from docs, cold ice pack on my temples and resting in a dark room is the combination that tends to work for me (only if I catch it in time otherwise the meds don’t work as well). Sumatriptan makes me very drowsy though so I have be at home (preferably in bed) before I take it. Have you been to doctors? x |
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"I would call it more health conditions than disabilities but I have asthma, IBS, gluten allergy, severe hormonal migraines, and chronic fatigue. Other than that I’m all good.
Have you ever found anything to help with hormonal migraines,they are nasty
They are absolutely dreadful aren’t they
Sumatriptan on prescription from docs, cold ice pack on my temples and resting in a dark room is the combination that tends to work for me (only if I catch it in time otherwise the meds don’t work as well). Sumatriptan makes me very drowsy though so I have be at home (preferably in bed) before I take it. Have you been to doctors? x "
Yes but with no joy,I didn't get on with sumatriptan and the only thing I have found that helps is syndol from the chemist now they have put the muscle relaxant back in it.
I absolutely dread them though! |
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By (user no longer on site)
over a year ago
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Health conditions I'd say, rather than disabilities, but employers etc consider them to count.
I have BPD, bipolar, OCD and I'm a recovering bulimic. These can be pretty severe and have landed me in hospital a few times.
I wouldn't wish them on anyone, but you learn to live with it. |
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"invisible disabilities dyslexia spelling is very bad but if you had to talk to me in real life I am very brain "
Same here. I use grammatical app, to help me with my spelling. But I don't consider it as a disability. |
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By *ouanna JoWoman
over a year ago
A little village |
"I would call it more health conditions than disabilities but I have asthma, IBS, gluten allergy, severe hormonal migraines, and chronic fatigue. Other than that I’m all good.
Have you ever found anything to help with hormonal migraines,they are nasty
They are absolutely dreadful aren’t they
Sumatriptan on prescription from docs, cold ice pack on my temples and resting in a dark room is the combination that tends to work for me (only if I catch it in time otherwise the meds don’t work as well). Sumatriptan makes me very drowsy though so I have be at home (preferably in bed) before I take it. Have you been to doctors? x
Yes but with no joy,I didn't get on with sumatriptan and the only thing I have found that helps is syndol from the chemist now they have put the muscle relaxant back in it.
I absolutely dread them though!"
Oh really, that’s shit.
Glad you’ve found something that helps though. I feel for you, they’re so debilitating. I’m written off for days at a time sometimes.. x |
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By (user no longer on site)
over a year ago
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"I have autism , which affects me mentally and socially , I'm very black and white , there isn't no grey ...I struggle to pick up on sarcasm and social cues.....but I'm lovely and easy to talk to and get along with "
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By (user no longer on site)
over a year ago
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Sometimes...well most the time , with my autism and the fact I struggle with social cues , I struggle to tell if anyone likes me or is making a move as I'm not great with subtlety , would rather be direct Haha x |
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"Sometimes...well most the time , with my autism and the fact I struggle with social cues , I struggle to tell if anyone likes me or is making a move as I'm not great with subtlety , would rather be direct Haha x"
Similar. Someone could be giving me a 'take me to bed or lose me forever' look. Or it could be 'I've had enough, go and bother someone else' tone of voice and I'd struggle to tell the difference! Although I've improved enormously as I've grown older.
Have you tried clubs? They are overwhelming at first but stick with it and you'll be glad you did. |
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By *smCouple
over a year ago
Liskeard |
I have fibro and arthritis/ dodgy knees means I can’t kneel or go on all fours for long so have adapted , my late husband had cerebral palsy, one side of his body was mostly in spasm or not working ,, we had a hell of a lot of fun finding the positions that worked for us , including tying his hands up to the bed lol
He never let his disability get in the way of doing something ,
His Moto was I’ll find a way or make my own . I try and live by that x
My fibro makes me beyond tired so sometimes having the Sub do all the work is great lol |
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By (user no longer on site) OP
over a year ago
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"I have fibro and arthritis/ dodgy knees means I can’t kneel or go on all fours for long so have adapted , my late husband had cerebral palsy, one side of his body was mostly in spasm or not working ,, we had a hell of a lot of fun finding the positions that worked for us , including tying his hands up to the bed lol
He never let his disability get in the way of doing something ,
His Moto was I’ll find a way or make my own . I try and live by that x
My fibro makes me beyond tired so sometimes having the Sub do all the work is great lol "
Your late husband sounds amazing what a wicked attitude. Bless him. |
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By *erces LetiferMan
over a year ago
Somewhere off the edge of the map... 'ere there be monsters |
"I have fibro and arthritis/ dodgy knees means I can’t kneel or go on all fours for long so have adapted , my late husband had cerebral palsy, one side of his body was mostly in spasm or not working ,, we had a hell of a lot of fun finding the positions that worked for us , including tying his hands up to the bed lol
He never let his disability get in the way of doing something ,
His Moto was I’ll find a way or make my own . I try and live by that x
My fibro makes me beyond tired so sometimes having the Sub do all the work is great lol
Your late husband sounds amazing what a wicked attitude. Bless him. "
Right? I raise my glass to him and all like him who keep on keepin' on. What a shining example to the world. x |
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"Is cancer and chemo classed as a disability? If so, count us in... If not.. Er.... As you were.. "
According to the Equalities Act, a cancer diagnosis is an immediate tick in the disability box, no matter what the prognosis. Come and join the rest of the Fab Ward for Slight Seconds |
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By (user no longer on site) OP
over a year ago
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"Is cancer and chemo classed as a disability? If so, count us in... If not.. Er.... As you were..
According to the Equalities Act, a cancer diagnosis is an immediate tick in the disability box, no matter what the prognosis. Come and join the rest of the Fab Ward for Slight Seconds "
Someone who knows their legislation yay! I’m battling with my employer at the min. |
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By (user no longer on site) OP
over a year ago
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"I have fibro and arthritis/ dodgy knees means I can’t kneel or go on all fours for long so have adapted , my late husband had cerebral palsy, one side of his body was mostly in spasm or not working ,, we had a hell of a lot of fun finding the positions that worked for us , including tying his hands up to the bed lol
He never let his disability get in the way of doing something ,
His Moto was I’ll find a way or make my own . I try and live by that x
My fibro makes me beyond tired so sometimes having the Sub do all the work is great lol
Your late husband sounds amazing what a wicked attitude. Bless him.
Right? I raise my glass to him and all like him who keep on keepin' on. What a shining example to the world. x"
You’re lush come and chat on kik I wanna take advantage of a tipsy you x |
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"Is cancer and chemo classed as a disability? If so, count us in... If not.. Er.... As you were..
According to the Equalities Act, a cancer diagnosis is an immediate tick in the disability box, no matter what the prognosis. Come and join the rest of the Fab Ward for Slight Seconds
Someone who knows their legislation yay! I’m battling with my employer at the min. "
Its rather sad, but I think I can quote the Act verbatim |
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By (user no longer on site) OP
over a year ago
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"Is cancer and chemo classed as a disability? If so, count us in... If not.. Er.... As you were..
According to the Equalities Act, a cancer diagnosis is an immediate tick in the disability box, no matter what the prognosis. Come and join the rest of the Fab Ward for Slight Seconds
Someone who knows their legislation yay! I’m battling with my employer at the min.
Its rather sad, but I think I can quote the Act verbatim "
Not sad at all useful. My boss was working with one of the ladies who helped found the act yet showed me zero sympathy or interest when I asked for short shifts and reasonable adjustments. |
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"Is cancer and chemo classed as a disability? If so, count us in... If not.. Er.... As you were..
According to the Equalities Act, a cancer diagnosis is an immediate tick in the disability box, no matter what the prognosis. Come and join the rest of the Fab Ward for Slight Seconds
Someone who knows their legislation yay! I’m battling with my employer at the min.
Its rather sad, but I think I can quote the Act verbatim
Not sad at all useful. My boss was working with one of the ladies who helped found the act yet showed me zero sympathy or interest when I asked for short shifts and reasonable adjustments. "
I must say that after an initial false start, my employer have been brilliant. Working at home reminds me daily of how accessible my workplace is and my home is not  |
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By *erces LetiferMan
over a year ago
Somewhere off the edge of the map... 'ere there be monsters |
"I have fibro and arthritis/ dodgy knees means I can’t kneel or go on all fours for long so have adapted , my late husband had cerebral palsy, one side of his body was mostly in spasm or not working ,, we had a hell of a lot of fun finding the positions that worked for us , including tying his hands up to the bed lol
He never let his disability get in the way of doing something ,
His Moto was I’ll find a way or make my own . I try and live by that x
My fibro makes me beyond tired so sometimes having the Sub do all the work is great lol
Your late husband sounds amazing what a wicked attitude. Bless him.
Right? I raise my glass to him and all like him who keep on keepin' on. What a shining example to the world. x
You’re lush come and chat on kik I wanna take advantage of a tipsy you x"
Oh my! |
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