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-   -   Hello lovely people! I have some symptoms after PCS to cheack pls.. (https://www.neurotalk.org/new-member-introductions/252917-hello-lovely-people-symptoms-pcs-cheack-pls.html)

Mack Pol 01-28-2019 07:51 AM

Hello lovely people! I have some symptoms after PCS to cheack pls..
 
Xxx

So in short I was a silly *** or still IAm and had 2 head Cunncussions
Fist proper one at rugby and I was put to sleep for 2 min and second 2 weeks later
When I fought I'm OK..when played and had big pressure to head...yes I'm stupid.
Since then 2 years a go...head aches ...went down in 70%..hurra

1. And still have some pressure relief sssiking noise sometimes in head..then felt some relief...is smaller now compare to my first months..uff
Sometimes I have bad taste in my mouth...
And when is heating on or drinking hot sup it affect it as well.... Yes I know I'm stupid.

2. When driving hard suspension affects my head..irritates me..same with eating after driving. Irritates me ..doctor
Can't help me much than prescribed Amitrypteline at night...helps and Steraline antidepressant recently...as they didn't know what they can do I didn't rest it when all this started as I was expecting my first child and I was working as field service engineer...to keep my family
.......,...when lifting 20kg sometimes pumps my headaches
after driving I'm more irritated..
Fumes from cars..strong smells trigger my head aches..like bleetch cleaner..
Fatigue is less now but not cleared
Brain fog can come to me letet in week when working.

Can I drink coffee tea or beer? Sometimes as doctor say I'm fine but I fell not 100%
I went thrue hell and hope noone will end up like me...but I know It could be much worse..
....is my drivibg damaging my brain as is 2 years and 4 months...can't get good night sleep
With out amitrypteline...and Setaline make me less emotional..
I'm 33 I loved my beer...I hope one day I'll ok

kiwi33 01-28-2019 01:49 PM

Hi Mac Pol

Welcome to NeuroTalk :).

I am sorry to read about your experiences with concussion.

The TBI/PCS forum (https://www.neurotalk.org/forum92/) is very active so I am sure that if you describe what you have experienced there you will get lots of support and good ideas from other members.

Best wishes.


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