No. They are not part of a panic attack and they are nothing like shivering
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Yep!
---------- Post added at 10:58 ---------- Previous post was at 10:30 ----------
What's that got to do with the price of fish? You said you don't fear ALS and obviously don't have twitching, so your dismissive comments aren't really helpful to those in the throes of this
Frankly everything. Twitches, spasms and a plethora of other physical symptoms are common in stress biology. If you go back and read the first post I made on this thread, that alone is enough to dismiss your fears, especially taking into consideration the amount of time that has passed since the symptoms manifested themselves.
I know first hand how stress affects one physically. Between my real illnesses and dealing with what happened to my wife, I had a laundry list of stress related physical symptoms including twitching. Thing is, I don't suffer with HA and I knew exactly what was causing it. As things calmed down, so did the physical reaction to them.
Positive thoughts
OK, sorry. It was a language misunderstanding though. I thought "twitches" was the same as spasms or shiverings. My bad. I am not a native English speaker.
edit: I really dont understand the big difference between twitches and spasms. It has to do with muscles being stressed anyway.
Read this, people. I think she might be related to you, Mel ;)
http://www.independent.co.uk/life-st...s-1623649.html
Hi,
This is kind of helping me with my anxiety. So thanks for that. I just need to think 38 is unlikely to get ALS without muscle weakness and twitching in lots of places makes it even less so. Doc said my reflexes were super normal although a few days before my friends kept saying your twitchy but I was super stressed and ill.
I just don't get this burning pain I am getting on the muscles. I had terrible flu 4 weeks ago wonder if I am still recovering from that.
Thanks anyway.
Mike
The Als / mnd rabbit hole is a nightmare! , I’m sure that many people will get reassurance from this post that will help , unfortunately though for many people suffering from health anxiety who fear this disease , no amount of medical reassurance works ( and this was certainly me ! ) I spent a year of my life scouring medical info , reading literally every post on the BFS site , trips to doctors , a neurologist and this didn’t help me , the anxiety makes you twist facts/ reality and not process information in he same way that someone without extreme anxiety would . I could have seen the biggest expert in the field and I know I would have come away reassured at first then the doubts would have started , words they had spoken twisted etc . I remember on my neurologist report it read there are no signs of MND , I twisted this into a negative -“ there are no signs yet etc !!”
For those of you not to deep in it , medical info / reassurance I’m sure will
Help , but those deep in it with health anxiety my advice would be try and break the reassurance cycle and focus on tacking the health anxiety , very very hard but doable!