I decided that it's time to update my status. I am and always have been PPSS.
I started progressing rapidly and 1988 when I was 38 years old, this was because my 18-year-old son died unexpectedly and an accident. So from approximately the 1990s, I only have use of my head and neck.
This is not been too bad to deal with as I have a great wheelchair that I drive by using my head. I put myself into a hospital for disabled people and it is great here! I have my own large room, television and laptop connected to will full-screen so that I can watch movies on DVDs etc.
The past few months I have been progressing again, new symptoms had laid dormant for so long I thought I was set for life. But, we all know better never let your guard down. But it was fun living in a fool's paradise.
Now I am meeting with a very nice speech therapist who will work with me on my "Dysarthria (speech) and Dysphagia (swallowing).
Well I have to stop for now, I'll write more on Sunday. Hope you're all feeling good! Go Warriors!.
I started progressing rapidly and 1988 when I was 38 years old, this was because my 18-year-old son died unexpectedly and an accident. So from approximately the 1990s, I only have use of my head and neck.
This is not been too bad to deal with as I have a great wheelchair that I drive by using my head. I put myself into a hospital for disabled people and it is great here! I have my own large room, television and laptop connected to will full-screen so that I can watch movies on DVDs etc.
The past few months I have been progressing again, new symptoms had laid dormant for so long I thought I was set for life. But, we all know better never let your guard down. But it was fun living in a fool's paradise.
Now I am meeting with a very nice speech therapist who will work with me on my "Dysarthria (speech) and Dysphagia (swallowing).
Well I have to stop for now, I'll write more on Sunday. Hope you're all feeling good! Go Warriors!.
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