Hi selly, I remember when hubby was first diagnosed feeling like it was all a bad dream and every time I woke up in the morning it was like a slap in the face that would literally take my breath away. A slap of reality that broke me every morning. Needless to say that feeling has thankfully passed and only hits every now and then. The friends aspect is so hard, hubby found the same thing that people just stopped coming over stopped calling. I suppose they didn't know what to say but as hubby pointed out one day "he was still the same person" . As for treatment I have had that conversation so many times before, if we didn't accidently find out how long could we have gone without anything changing. Unfortunately for us the diagnosis is not good and hasn't been from the start , so some days I wish we never knew so we could have continued with life the way we were. Although the strength mentally emotionally and physically that my husband is showing amazes me every day and I am so proud. As for my babies they are amazing and are the reason I keep going. Take care and it's good to know we are not alone! Ox
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