Good morning! I was actually eager to get out of bed this morning because I looked forward to see what everybody was talking about today. I just joined last night, so I'm like a child with a new toy. Nobody in my house truly knows how I feel on a daily basis. They know that I hurt and they are supportive, but they can't even begin to understand; sometimes I don't. I would like to hear from someone who has to use a wheelchair. I feel like I am heading in that direction. How confined are you and how did you get your mind in gear for the inevitable, or is it inevitable?
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As I sit here this morning in the pre-dawn hours and write these thoughts, I am reminded of how my wife would often wake up early to send me a text,or a link, or an I love you note that I would see when I woke up.Today is day 61 without my love of my life. I am learning to cope, and trying heal but this is truley a walk through Hell. I try to honor my wife by staying strong, but at times I feel...
I was diagnosed with Temporal Lobe Epilepsy a couple of days ago. Apparently the Deja vu and nausea episodes I have been having for the last 7 years or so are actually seizures. Thankfully, because I have only ever had focal aware seizures I am allowed to keep my licence. However I am struggling to come to terms with the diagnosis. It doesn't really seem real. I'm interested to know how others...