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Sufferer New. lou gehrigs/als caregiver to late wife

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Hello All: After being diagnosed with " Caregivers PTSD" I feel like Ive been labeled in a Way. I knew being the primary caregiver for my late wife who had ALS was taking a toll on Me but just didn't have the time to think about what the effects would be after her passing away. It's been almost a year and after trying to get my head straight on my own I did seek professional help. Tried a couple Meds that just made me feel sick and dizzy. Back to just doing my Best on my own. Is it " Normal " to feel like your about to explode? Or having tremors? I'm going to just start reading posts. Thanks in advance for anyone reading this. And for any insight and support I may find here.
 
Welcome to the forums! I'm so sorry about the loss of your wife. ALS is horrible. I'm glad you are reaching out for support. Are you working with a solid therapist? It could help reduce your symptoms and lengthen the fuse before exploding. And yeah, my hands shake quite a bit too. A grief support group might be a good option too to explore as well.
 
Sorry for the reasons that led you here, but must say you've landed in a good space for learning more and finding support. So many deeply resonate with what you feel. Welcome, and I share my sympathies in the loss of your wife. I'm glad you were there for her.
 
Yep, hand tremors trying to hold back the rage.... you are in the right place.... and we understand good days too by the way !!
Welcome !!!
 
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