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Fibromyalgia

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By *weethearts.of.midlothian OP   Couple
44 weeks ago

Edinburgh/midlothian

Hey guys and gals. I'm sure I'm not the only one on here who suffers from this god awful affliction. Anyone have tips or tricks for flare ups? And does it inpead your sex lives?

Thanks in advance

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By *tb28Man
44 weeks ago

mount vernon

I help to treat this at my work. I have done some work with the fibro charity as well. If you want more information feel free to pm

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By (user no longer on site)
44 weeks ago

Me too Fibromyalgia and MECFS. If I’m having a flare then yes I don’t feel that sexy.

For me it’s managing and recognising my limits. Like I’ve just came back from a holiday in Lisbon and push myself so new the next few days would be sleep and rest x

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By *weethearts.of.midlothian OP   Couple
44 weeks ago

Edinburgh/midlothian


"I help to treat this at my work. I have done some work with the fibro charity as well. If you want more information feel free to pm"

Thanks

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By *weethearts.of.midlothian OP   Couple
44 weeks ago

Edinburgh/midlothian


"Me too Fibromyalgia and MECFS. If I’m having a flare then yes I don’t feel that sexy.

For me it’s managing and recognising my limits. Like I’ve just came back from a holiday in Lisbon and push myself so new the next few days would be sleep and rest x

Thank you

"

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By *assy LassieWoman
44 weeks ago

Near Glasgow


"Me too Fibromyalgia and MECFS. If I’m having a flare then yes I don’t feel that sexy.

For me it’s managing and recognising my limits. Like I’ve just came back from a holiday in Lisbon and push myself so new the next few days would be sleep and rest x

"

I agree. I always need to factor in prep and recovery times around any days or nights out.

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By *r Cheeks GlasgowMan
44 weeks ago

Glasgow

I have fibromyalgia and my life is pretty rubbish as others who have it will know.

I still want to be sexual but find it difficult meeting up etc cause I never know one day to next how I’m gonna be and I’m definitely not going to be throwing anyone around the bedroom lol

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By *andy_FraserTV/TS
44 weeks ago

Edinburgh

My partner has recently been talking about skeletial pain, and my first thought was fibromyalgia. What she described sounded so much like what a friend with fibromyalgia said it was like (back in her early days).

However she's on so much medication and has so many other things wrong with her, I didn't want to suggest it, and add to any woes.

She is speaking to her GP and specialist consultants though, so I suspect they'll come to some form of conclusion.

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By *tirlingbenMan
44 weeks ago

Stirling

A friend swears by CBD oil, says it really makes a difference

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By *r Cheeks GlasgowMan
44 weeks ago

Glasgow

Tried cbd didn’t like it

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By *angbuddyMan
29 weeks ago

Chippenham

I suffer from this too, my form of prescribed meds are not for everyone. Message me if you wish

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By *rincessArielWoman
16 weeks ago

The bottom of the Ocean

Fellow fibro warrior here!

I had an amazing meet yesterday evening while I was feeling good. But new I'd be paying for it today. And true to form I have slept pretty much all day.

You just need to listen to your body. If it's telling you to rest then maybe organise that gang bang for another time. Lol

Also all my close friends on here that I meet with regularly know about my fibromyalgia and are really supportive, especially if I'm having a bad day and have to cancel on them. Xx

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By (user no longer on site)
16 weeks ago

It put an stop to my wife’s interest on being on here , was a long time ago , it’s taken a few years for her to get a bit of drive back but still has bad times , she tries to be positive, I just don’t push her at all

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By *witchywomanWoman
16 weeks ago

GLASGOW

It can be tough, but knowing re aftercare and having limits in place that things change all the time helps. And for them to understand that you responding one way one time doesn't mean it will be the same the next. I do a lot of alternative things to help keep me going too.

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By *oaby AyrshireMan
15 weeks ago

Ayrshire

Had fibro for nearly 15yrs, the best thing to help is to listen to your body always ! Not someone telling you to do this, that or the other especially when they dont have fibro! Not all fibro warriors suffer the same symptoms but its always good to talk to other fibro suffers who might get relieve doing something one way or the other way that maybe might help. Whenever im asked about it ,told I look fine , get a job etc my response is always the same....

" If you dont have it , you will never understand it , now fuck off! Works a treat for me rather than try and explain why I can walk one day and not another !

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By *witchywomanWoman
15 weeks ago

GLASGOW


"Had fibro for nearly 15yrs, the best thing to help is to listen to your body always ! Not someone telling you to do this, that or the other especially when they dont have fibro! Not all fibro warriors suffer the same symptoms but its always good to talk to other fibro suffers who might get relieve doing something one way or the other way that maybe might help. Whenever im asked about it ,told I look fine , get a job etc my response is always the same....

" If you dont have it , you will never understand it , now fuck off! Works a treat for me rather than try and explain why I can walk one day and not another ! "

Totally agree!

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By *lex and dollCouple
12 weeks ago

Falkirk

Female friend didn’t work for year and a half with it but someone put her onto the cbd oils but she had to research them to get the strongest ones available. She said there is a huge diffrence in strength. But when she found the correct one it turned her life around and almost took all the symptoms away

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By *oShrinkingVioletWoman
12 weeks ago

the land of unicorns and fairytales

I’ve been suffering with fibro for years

The worst thing about fibro isn’t the pain or the fatigue but the things you lose !

You become unreliable, you struggle to make and keep plans, you struggle to get out of bed some days

You lose partners/friends - they don’t understand, they get sick of you skipping off early, they get annoyed at you turning up late, changing your mind last minute or simply not waking up and missing things, your now boring cause you don’t drink or wanna go dancing you prefer something slower and chilled, they take everything personal and think you’re finding excuses not to show up

You lose jobs - you’re off sick lots, you can’t function the same anymore and make mistakes at work or take longer to do your job, you miss lots of days and don’t phone in sick because you never actually woke up

You lose your confidence - you feel old, you feel boring, you feel drained, you don’t want to spend hours getting ready, you just want to be comfortable and chilled, without the war paint on you don’t feel quite ready for battle

You lose your drive/ambition - you no longer feel the same about things like this because you’re worried in the back of your mind about how it’s going to affect your fibro, that adventure you would have jumped at the chance of before you start overthinking it and stressing about it and talk yourself out of it

You lose your independence - if you’re going through a particularly bad flare you can’t do everything you could before, have to ask people to help you, can’t go shopping alone, can’t tidy your house by yourself, struggle to make meals, struggle to go for a shower

And the list doesn’t stop there !!

Then there’s the whole negative impact all of the above has on your mental health !!

The constant grief over the things you’ve lost, the low feeling of self worth, crying over the things you’ve lost can’t do but feel you should be doing

And then to top it off you have folk saying to you it can’t be that bad, everyone gets tired working full time, but you were fine last week, how can you do that if you have fibro, you don’t look sick to me, I know someone with fibro and they still work full time and go out and do everything else no problem

Could go on all day about how fibro affects a person but only from a personal perspective because everyone else is different

Biggest thing for me about fibro is learning that when I have my good days don’t hang about waiting for people to show up !! They don’t put anything on hold for you when you’re ill, they don’t change plans to accommodate you so why wait for them ! Jus get out there and do what you can today and fuck everyone else

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By (user no longer on site)
12 weeks ago

My reply after NSV’s lived experience post will look shite but il put it anyway.

I lobe with CRPS in both my legs which is pretty rare and is also a bit of a c*nt. whilst CRPS and Fibromyalgia are different they do have some similar traits and symptoms. I found that heat therapy helps but I can’t overdo that as the muscles swell and I get compartment compression symptoms

To entirely contradict that though, cold water dipping did have huge benefits for me but I noticed that this slightly reduced the pain whilst enhancing the fatigue so I packed that in.

The best thing for me is a weighted blanket on the high pain days.

To put some slight humour in, to get the weighted blanket effect whilst getting some attention, I let my sausage dogs up and they sleep on my legs if I get all the blankets out

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By *oShrinkingVioletWoman
12 weeks ago

the land of unicorns and fairytales


"My reply after NSV’s lived experience post will look shite but il put it anyway.

I lobe with CRPS in both my legs which is pretty rare and is also a bit of a c*nt. whilst CRPS and Fibromyalgia are different they do have some similar traits and symptoms. I found that heat therapy helps but I can’t overdo that as the muscles swell and I get compartment compression symptoms

To entirely contradict that though, cold water dipping did have huge benefits for me but I noticed that this slightly reduced the pain whilst enhancing the fatigue so I packed that in.

The best thing for me is a weighted blanket on the high pain days.

To put some slight humour in, to get the weighted blanket effect whilst getting some attention, I let my sausage dogs up and they sleep on my legs if I get all the blankets out "

Sending hugs

Nothing else that trying to find something that works, I loved the cold water therapy however my raynaulds is worse than ever now, it’s no longer just the cold that affects me but the lack of circulation so something as simple as my hand being bent at an angle for too long and the fingers go numb, heat therapy is amazing until I try to stand up and my BP sends me crashing to the floor.

I do love the idea of a weighted blanket though I defo find when I’ve left my ironing on the bed and my covers are tight because of it I sleep better always thought it was because self consciously I was feeling like I was sharing the bed

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By *rWriter1286Man
11 weeks ago

Hamilton

As one of the rare males with fibromyalgia I can understand the frustration with it. I think the unpredictability of it is what gets me at times. The flare ups that happen for no rhyme or reason. Hope you all feel better soon with it.

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By *hatwedointheshadowsWoman
11 weeks ago

back’o’beyond


"Hey guys and gals. I'm sure I'm not the only one on here who suffers from this god awful affliction. Anyone have tips or tricks for flare ups? And does it inpead your sex lives?

Thanks in advance "

For me I have found the electro wand helps the electric stimulates the nerve endings in the skin and the day or 2nd day after I feel it helps and going to club settings with equipment to help with support like a spanking bench has helped me lot xx

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By *hills2017Couple
11 weeks ago

Newport

fella has had fibro for 20+ years tried so many different things to the point that the dr gave up on him last few years managed to get him a prescription for his fibro and other issues from a private clinic for medical cannabis that has changed his life around to the point that we have been able to start travelling the uk and have accomplished a lot of miles on the 2 wheels and getting back out available for the single ladies to join us he still has his major flare ups but they are more manageable and we are able to plan around them helping distract it as well does help

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