I get shocking muscle spasms still and everywhere, I only just found this out a few months ago. I was advised by a naturopath and nurse friend to buy a bottle of magnesium oil spray- ( never heard of it) it's not oily...it's just the name, it's awesome, I either spray it on the muscle and rub it right in or spray it on my hand then rub it in a sore or spasming muscle, depending on wether I can reach it with the bottle, really good for pain too, I honestly couldn't believe how quick and good it was. I do take magnesium tabs twice the daily dose but this being topical it goes right to the spot and doesn't get diluted via any organs..it's quite xpchap too- it's really only Epsom salts. And we all know how good a soak in a ES bath is, hope you find what works for you soon, we are all so different, be blessed sarapainfree, have a lovely day.😘💐💐
Thank you I love nothing more than a long hot muscle soak bath every nite I use deep freeze jels for.my pain and also a hot wheat bag sometimes helps especially with my neck I too suffer with the spasam all over and only two weeks ago it started to effect my back and muscles around the spine and had a ambulance called as I couldn't walk doing much better now that side of it has settled down many thanks take care I will look in to the oil as well
Oh that process is designed to put people off.
Just keep in mind that the general acceptance among medical professionals involved with fibro is that very few sufferers improve over time the majority either stay the same or deteriorate..
Whilst at bad news for us sufferers it does give weight to any future PIP claims once you have had the first one accepted
They would be hard pressed to argue to the contrary in any appeal.
Well fingers crossed it all gets excepted I have given them anuff evidence to back up everything iv told them will keep u updated
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This is what I did, I allowed them to contact my gp and get my records as back as they wanted, I had nothing to hide, so they asked for me to sign over all my medical records even for the past 12-18 months,that's what they did and they couldn't believe the amount of notes, however that totally went in my favour as it was all down in black and white, every visit to me doctor was inside there, the dwp said, 'o my goodness this person is really unwell'
i was able to prove my limits and my needs on a day to day, I've been relying on friends and family for a good time now mainly because I didn't want to appeal at the board as it was making things so much worse
I was given diazepam due to cramps and sprains on all my nerves mainly head, hands and shoulders, the spasms are ridiculous, I took 2, and I can honestly say they gave some kind psychotic break, I had imaginary friends, I was calling my family and nothing made sense, thankfully ,there are so many people fforgiving me as they realise iit was out of my control
thank god for family and friends, and obviously all you wonderful people here
Well iv given them letters.off go and hospital I was awarded standard rate care and mobility last year but have recently got worse where I ended up with a ambulance and at hospital so fingers crossed this will all go on my favour but u just never know with the Syston these days u do the rite thing telling them if u get worse but it's all a gamble and the assessment people are not so nice either