Noticing more and more symptoms, should i be worried or am i just being overly dramatic?
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As i have previously stated in other posts, i am very recently diagnosed with CFS/M.E. Struggling to get the correct treatment and hold down a full time job etc. I have noticed of recent other symptoms which i have either never previously had, or not had often enough to cause me concern. I get regular periods of dizzy spells much more than ever before and i'm noticing that sometimes i just forget how a word is spelt or pronounced or what something is called. Most worryingly for me is that i get the shakes which i have never previously noticed- at least not to this extent. I've had it crop up occasionally but its gotten noticeably more frequent and quite bad at times. My hands are usually where i get the bad shakes. My heart palpitations (which i LOATHE!) have come back quite badly too, and when i have the shakes my heart flutters like mad. I've just had yet another full round of bloods tested and still come back all normal (Hence the CFS/M.E diagnosis. It's taken many years to even get to the point of diagnosis and now i'm fighting a whole new battle just to understand my symptoms and the condition itself. I'm 25, i feel like i'm 75 some weeks. Are any of my symptoms just standard for some with M.E or does anyone think it could be something else/different??
0 likes, 10 replies
Sellins sarah-loui069
Posted
My experience is that you have to treat the symptoms of ME as there is no cure all. I hate mindfulness but it works for some. I found seeing a psychologist very helpful. Be organised, keep lists, spread the load.
sarah-loui069 Sellins
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andrew_08416 sarah-loui069
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I have the same issues amongst others. for me the shakes and dizzyness get worst as the day progresses usually always with muscle weakness and when I push myself to do more. I've the same cognitive issues reglardless of the time of day but also gets worse the more tiered I get. as a child I used to stutter, I learnt how to control the stuttering with concerntration.
But as you probably guessed- I am back stuttering as an adult.
I think humaour is a great thing, my wife and my friends are very supportive. and if I cannot think of the word or find an alterative then the word becomes Bob. easy to remember and impossible to stutter. :-)
if your still worried then do get it checked out.
sarah-loui069 andrew_08416
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artistmike sarah-loui069
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What you are describing are the standard symptoms that most of us suffer from, in some degree or another, and they will increase in severity the more that you do.
I think the main advice that all of us here would give would be to start giving up some of the things you do and learn to take things a good deal more easy. 'Battling on' and 'working through it' don't work with ME/CFS and if your symptoms are getting worse it's a sign that you're overdoing it...
I've had this condition for about fifteen years and I'm still learning about it but one thing I know, you need to find a level plateau at which you can function optimally and then not stretch yourself beyond what works for you and make your symptoms worse and that way you have a good chance of some slow improvement.
It will take time though and you'll have peaks and troughs en route but pacing and rest are your best friends, and physical and mental stress your worst....
sarah-loui069 artistmike
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Ravenwood sarah-loui069
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sarah-loui069 Ravenwood
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artistmike sarah-loui069
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I would make that a priority above everything else. With support from a good doctor you'll find it far easier to deal with friends, family and above all work.... At the moment all you seem to be doing is being forced to make your health worse, which isn't the way it should be....
You should not be apologising to anyone for being ill and you badly need support but it's up to you to create the environment whereby you receive that support, and don't tolerate a doctor who doesn't know his job, there are some good ones out there who will help... :-)
Ravenwood sarah-loui069
Posted