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I have been writing a blog for the last 2 months or so about my experiences with MS. I am in my late 20's, diagnosed this year (2011).
My blog is not for everyone, there is some crude language and topics. But the blog is 100% honest. I hold nothing back. I don't reveal my name or too many personal details and that allows me to be a little more open, and discuss things that I probably wouldn't talk about in detail otherwise.
I have discussed sex, depression, medications/drugs, etc..
There is a steady flow of traffic and comment discussion there.
I am in a rough place in life right now and that has left me a bit cynical and that comes out a bit in the writing.
People seem to like it because it's not peaches and cream. It is as real as it gets and again, nothing is held back (except my identity).
I thought I would share it here in case someone of the younger crowd finds something that they can relate to.
Other newly diagnosed have to have some of the same thoughts, feelings and issues that I have.
There is a popular posts section on the right side with some topics that might be good reading. Also I am on Gilenya if you are looking for info on that. I was on Rebif, which was the worst experience of my life.
The tag on this site is that it's not your Mom's MS Blog...Hope someone finds it helpful.
I have been writing a blog for the last 2 months or so about my experiences with MS. I am in my late 20's, diagnosed this year (2011).
My blog is not for everyone, there is some crude language and topics. But the blog is 100% honest. I hold nothing back. I don't reveal my name or too many personal details and that allows me to be a little more open, and discuss things that I probably wouldn't talk about in detail otherwise.
I have discussed sex, depression, medications/drugs, etc..
There is a steady flow of traffic and comment discussion there.
I am in a rough place in life right now and that has left me a bit cynical and that comes out a bit in the writing.
People seem to like it because it's not peaches and cream. It is as real as it gets and again, nothing is held back (except my identity).
I thought I would share it here in case someone of the younger crowd finds something that they can relate to.
Other newly diagnosed have to have some of the same thoughts, feelings and issues that I have.
There is a popular posts section on the right side with some topics that might be good reading. Also I am on Gilenya if you are looking for info on that. I was on Rebif, which was the worst experience of my life.
The tag on this site is that it's not your Mom's MS Blog...Hope someone finds it helpful.
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