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11 Aug 20, 10:37 PM |
#11
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Thread Starter
VIP Dibber
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I've had fibro for quite a while and I've learnt to take it day by day- I have bad periods and then better ones but the last year my symptoms seem to be getting a lot worse to the point that some days I'm in so much pain or so exhausted I struggle to even get out of bed.
I'm not expecting much out of it I kind of feel its going to be going over a lot of the things I already know/do at this point but I'm willing to give it a try |
11 Aug 20, 10:48 PM |
#12
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Imagineer
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This might sound odd but have you considered reflexology ? I had weekly treatments when my depression was at its worst and I felt genuine relief for a couple days thereafter. It didn’t ‘cure’ me but just alleviated the symptoms enough for me to think straight and relax enough for a good nights sleep.
Might be worth researching to see if it’s a recommended holistic treatment. For your condition. |
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11 Aug 20, 10:48 PM |
#13
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Thread Starter
VIP Dibber
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I'm still learning to live with it its a ever changing journey with ups and downs and twists and turns you can only take it a day at a time.
I have found I seem to suffer far more with other ailments and that they can trigger the fibro which in turn makes other things worse. Something as simple as a cough or a cold can trigger a flare up and wipe me out for weeks or even months It must have been a hard decision to give up work but you need to do what's best for your health |
11 Aug 20, 11:03 PM |
#14
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Imagineer
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mandco
It’s the weather that sends me off at Times a 3/4 day spell of nice weather ie warmbut not too hot no sudden dips in temperature then it’s chucking it down cold and the worse bone chilling damp and im floored sore all over even going to,the toilet and our en suite has a higher toilet grab rails elbow taps motion sensor soap dispenser etc It can be equal to a Everest expedition for me Don’t even go,there with getting the necessary clothing down at times in a flare I wear A maxi dress or cafdan going commando round the house if need be I know TMI for most but I’m sure I’m not ot the only one who has too |
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11 Aug 20, 11:18 PM |
#15
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Thread Starter
VIP Dibber
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11 Aug 20, 11:39 PM |
#16
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Imagineer
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I’m so lucky I don’t get=the headaches that most folks do but=I find screen time if I’m in s flare can make things worse Alexa is your friend at times from putting on lights when the darker nights come in audio books music and my biggest helper the slow cooker no more faffing with heavy dishes from the oven
I’ve got a cooker hot /cold tap DH uses it more than me the tea or coffee tastes lousy if you use it it be great above the hob for filling pots etc for me but honestly is of no use to me right now |
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