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1 year - VNS update.

Today marks 1 year since I got my VNS - Vagus Nerve Stimulater for my epilepsy. Now this one year hasn't been the best so the results from the device is hard to tell if it's working. Not only have I had so much on my mind that every time I would have a seizure or a Ora that remembering to use my bracelet to set off the device has been hard.  I was hoping that when I had this surgery I would have had better results. 
Things in life happen, as my doctor understands that my body can't handle stress, getting sick, lack of sleep. 
So within this 1st year of having my VNS I've had 5+ seizures that doesn't count the ones that I don't know about.  
I was looking forward to going through this next treatment with all my loved ones. But unfortunately an important person decided to leave my life and my families life that was unbelievable. So that choice made a huge affect on how this new therapy(vns) was going to go. 
As of now I'm going day by day and today marks the start to a new year for my VNS. So let's see how this year goes and the results of round 2. 
Thanks to my family, boyfriend & friends for supporting me. I couldn't ask for anything else. 

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