SLEEPING up to 15 hours-a-day, feeling too exhausted to eat and covered in painful rashes, fibromyalgia has left Emma Gregory feeling like an old woman at just 31 years old. The former personal trainer, from Merseyside, now faces an added battle with people who dont believe shes ill, because shes too pretty to be sick.

SLEEPING up to 15 hours-a-day, feeling too exhausted to consume and covered in painful rashes, fibromyalgia has left Emma Gregory feeling like an “outdated woman” at just 31 years old.

The former personal trainer, from Merseyside, now faces an added struggle with individuals who don’t imagine she’s ill, because she’s “too pretty” to be ill.

Fibromyalgia is a long-term situation which reasons pain far and wide the frame. 

Symptoms include pain, stiffness, problems with sleep and headaches – however there is no cure and the purpose is unknown.

Speaking to Fabulous, Emma, who was once identified with the condition in 2019, opens up about her painful enjoy…

Two years ago, life was once completely different to how it is now. I was a full-time personal trainer, working out at least once an afternoon and dealing in a gym. I’d eat up to 2,500 energy an afternoon to gas my workouts, and felt are compatible, strong and healthy. 

Now, I’m trapped at home, sleeping for up to 15 hours-a-day and struggling to in finding the energy to even devour. Even a gradual yoga session is steadily too tiring. That’s what fibromyalgia has completed to me.

Two summers in the past, I started to notice I was feeling completely exhausted for days after a gymnasium consultation and had in point of fact swollen muscles. 

I attempted to ignore my expanding fatigue as I thought it used to be simply me getting a little older, as I was drawing near my 30s. 

But then it started getting worse and worse. I started to feel totally exhausted and tired virtually all day to the point I wasn’t in a position to entire fundamental tasks like converting the bedding, let on my own move to the gymnasium.

What is fibromyalgia?

According to the NHS, fibromyalgia is a long-term condition that causes ache everywhere the body.

As neatly as widespread ache, other people with fibromyalgia may additionally have:

  • increased sensitivity to ache
  • excessive tiredness (fatigue)
  • muscle stiffness
  • issue snoozing
  • problems with mental processes (referred to as “fibro-fog”), akin to problems with memory and concentration
  • complications
  • irritable bowel syndrome (IBS), a digestive condition that causes stomach pain and bloating

When I went to the medical doctors, they initially concept it will be Multiple Sclerosis.

During my journey in opposition to an actual prognosis, I used to be taking packets of paracetamol and ibuprofen a week to try and keep watch over the ache. 

After a spherical of assessments, I used to be relieved to uncover it wasn’t MS. But instead, I was identified with Fibromyalgia, ultimate February, just prior to the pandemic began. 

Honestly, I do not know why I advanced it then. The situation can be prompted by a aggravating revel in – I’ve skilled relationship breakdowns and the demise of close family member, but that was all in the past.

(*15*)

I was happy in my process, and living with my partner, 31. I hardly knew the rest in regards to the situation myself – no person in my family had it, but I always gave the impression to be the one who used to be ill. 

Eventually I was prescribed Pregabalin, which is a drugs for nerve pain.

I’ve been taking it for a year now however except in brief improving things initially, my symptoms have were given worse.

Over the ultimate six months I have been experiencing more pain and fatigue and the swelling in my joints began. 

I had my worst pain flare-up just prior to Christmas. I was feeling really tired and tired, and I couldn’t assume directly.

I saved going dizzy and I didn’t know what I was doing day to day. I was so forgetful and disorientated. I might take a seat down to flip the TV on after which couldn’t take into accout how to work the far off.

All my joints hurt and began to swell up in a number of puts, particularly my ankles.

Plus, after I’m having a ache flare-up I am getting rashes on my face, my arms and on my legs.

The pores and skin is going very pink and blotchy and then it will get dry and cracks. The rashes in reality smash my self assurance as they're very visual and actually uncomfortable. 

I’d already had to surrender my process as a PT to grow to be an workplace administrator, after which that came to an finish too in March 2021.

I discovered using to paintings truly painful as my toes harm if I’m in the similar place too lengthy, and had to take a whole lot of unwell depart, which is exhausting while you’re trying to get on. 

The drawback is, aside from the rashes, fibromyalgia is an invisible sickness. People don’t imagine you are ill because there are no obtrusive physical signs to the outside international.

At paintings it’s such as you’re a hindrance, they just think, “Oh crack on”. They don’t perceive when I say my legs are hurting. 

I’ve been told I’m too pretty to be ill and I’m in the ‘high of my life’. People say things like, ‘How can you feel so ill and appear to be you do?’

Just as a result of I’ve been ready to put makeup on, doesn’t imply I’m now not in pain.

I simply need people to let me have something – I’m too ill to pass on circle of relatives walks, bike rides or socialise, a minimum of let me wear some make-up to make myself really feel higher.

People don’t remember that inside of I think like an previous woman and beneath my garments my joints are swollen and throbbing, and my skin is itchy and cracking.

Just because I’m slender with a suntan, other folks don’t realise I’m in ache, residing with brain fog which makes it unattainable to assume immediately.

Sometimes I believe like screaming, I’m slim now not because I work out or I’m on some fancy vitamin, but because half the time I think too ill to devour or too drained to get ready a decent meal. 

No-one dares inform me they don’t believe me that I am ill, however you'll be able to tell from their expressions every so often, they think I’m making all of it up.

I hear other people complaining about lockdown and announcing the way it’s doing their head in, however for me lockdown is now not that other from commonplace life with this illness. 

Mentally that may make me feel very isolated, that nobody actually understands what I’m going through and that infrequently makes me really feel very down.

I’ll admit I've had a few moments once I really feel I just can’t lift on like this anymore. But my instant circle of relatives, boyfriend and close buddies have been truly supportive and feature learn up about the situation so they are able to strengthen me higher. 

In truth, it was my mum who read in The Sun a few cream referred to as Celafen, which is made up of fatty acids, and suggested I try it to see if it will possibly ease the ache in my muscle tissues and joints.

When I used it for the first time I felt it right away pass into my muscles and the pain started to ease within 20 mins and stayed away for many of the evening.

I’d had critical ankle and foot ache for two weeks and it right away eased the swelling.

In the first 12 hours I carried out the cream a few occasions, and after 24 hours I could actually stroll upstairs without a huge combat and get my swollen ft into my footwear. 

It’s helped me cut back my painkiller use through about 50 per cent. Plus, I’ve seemed into diet and discovered that gluten could make symptoms worse.

At one level, doctors concept I had IBS as I was having so many tummy troubles, but it could be that there is a hyperlink between gluten intolerance and fibromyalgia. 

There’s no cure for fibromyalgia, however no less than the cream and my vitamin are in reality helping to ease my symptoms.

  • Actimas Celafen, £10.50 for 50ml, from Actimas – buy here

I’ve found a new task merchandising which I will do from home and that’s truly boosted my mood.

Before that I was actually at my lowest, at house with not anything to do.

I’m not the type of individual to need to go on PIP (receive advantages reinforce for other people with disabilities & long-term illnesses) – I really like to paintings and keep busy. It provides me a routine and takes my mind off the fact I’m sitting in the home. 

Some days are higher than others, and I try to experience life when I will.

I’m hoping to have youngsters sooner or later, despite the fact that a part of me is anxious that it's going to be so tiring pregnancy.

But I check out to stay certain, and I’ll always be proactive in trying to to find things that may make my condition higher and extra bearable – and I proportion my tips about my Instagram page, so I can assist others going thru the similar factor. 

Emma Gregory has been using Actimas Celafen, £10.50 for 50ml to be had from actimas.co.uk

Where to get fortify

The NHS lists a lot of organisation which will help sufferers.

Fibromyalgia Action UK is a charity that provides data and make stronger to other people with fibromyalgia.

If you might have any questions on fibromyalgia, call the charity’s helpline on 0300 999 3333.

The charity also has a network of native support groups you could to find helpful and an online community, where you'll be able to learn about information, events and ongoing research into the situation.

Another fortify crew UK Fibromyalgia.

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And this woman was trolled for having fibromyalgia – other people call her an attention-seeker & even her friends reckon she’s making it up.

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This post first appeared on Thesun.co.uk

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