Posted , 4 users are following.
Hi,
So 6 months into being diagnosed with post viral fatigue. What I want to know is it possible to detect issues with the brain in people with ME should they get a brain scan ? Thanks
0 likes, 8 replies
Posted , 4 users are following.
Hi,
So 6 months into being diagnosed with post viral fatigue. What I want to know is it possible to detect issues with the brain in people with ME should they get a brain scan ? Thanks
0 likes, 8 replies
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JerseyKaz david59662
Posted
david59662 JerseyKaz
Posted
jacquie14742 david59662
Posted
I had an MRI done due to twitching and neuro symptoms, i think to rule out MS. They found no lesions but did find a pineal cyst...not much is known about these, but i was offered no follow up treatment fo this. I think its good though as Jersey Kay said to rule out other possibilities....do you get twitching?
david59662 jacquie14742
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If they don't then what ? Surely if i mention neurological symptoms i should get an MRI ? I've had tons more energy the past few days, been taking the D-Ribose 5g 3 times/day with 200mg of high quality coq10(ubiquinonoe). Started juicing organic only veggies too. I realise i can't expect an overnight cure but maybe just maybe one month or two or three. When you get no treatment form the GP what do you do ? I say completely saturate the body with as much nutrition as possible. Get fresh air, relax, good company. Omega oils are so important too, hemp and coconut and those from fish. So been feeling better so watch this space. Lots going on with me at the moment in terms of tests etc
jacquie14742 david59662
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JerseyKaz david59662
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It sounds like the shaking thing (especially if its around the same time each day) would be more likely to be a blood sugar or thyroid issue? I had the lyme test too, and the myasthenia for good measure!
JK
david59662 JerseyKaz
Posted
jackie00198 david59662
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