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Hi

Just wanted to empathise with you. I too have had CFS for many years

and then Fibromyalgia since 1999. I never knew we had so many

muscles, tendons and ligaments but every day I have pain in some area

of the body. I have just looked at my nail beds - no moons! Also I

was told that people with CFS/Fibro have altered finger marks. Just

wondered why this is the case. I can fully sympathise the exhuastion

is overwhelming, together with all of the other symptoms.

I was once told by one doc that we are like a sinking ship due to

having too much cargo on board. If we dump some cargo overboard,

then the ship has a good chance of rising up. I hope that switching

from Thyroxine to Armour will be like dumping some cargo overboard

and give me the chance to float (so to speak) and be able to tackle

the CFS/Fibro symptoms.

Love Caroline

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