I have only been on this site for a few months. I have been diagnosed with transverse myelitis and MS for four years so what I deal with is still fairly new to me.
Many people ask questions about meds or symptoms that they have. Some write about how they are feeling, emotionally and physically.
This is what I have enjoyed about this site. It has given me a better perspective about MS and how it affects everyone differently and about the real struggles we go through with MS that no one else can understand.
I don't mind reading the jokes. The laughter is great medicine.
I didn't think there would be so much pettiness. This is a tightknit group. Many have been on it for years.
I kind of keep myself in the background. I will stay on this site and hopefully I will read more about dealing with MS; ups and downs, jokes, pictures!