Squeezing the MS lemon...
During those six uncertain years, when my diagnosis hung in the balance, I started an online community for people like me.
I first started using the Internet in 1995. I quickly discovered that it was a great way to make contact with other people with MS.
At that time there wasn't a website that could put you in touch with people who shared your symptoms or interests. So I decided to start a website myself. I called it Jooly's Joint.
Jooly's Joint is almost 12 years old now and has tens of thousands of members from all over the world. It is a huge blessing in my life, an enormous responsiblity and a privilege to be a part of.
Had I not gone through those miserable years of uncertainty about my diagnosis, then Jooly's Joint might never have been created.
I'm still not glad that I have MS. But I feel incredibly blessed to have been driven by MS to create Jooly's Joint.
During those six uncertain years, when my diagnosis hung in the balance, I started an online community for people like me.
I first started using the Internet in 1995. I quickly discovered that it was a great way to make contact with other people with MS.
At that time there wasn't a website that could put you in touch with people who shared your symptoms or interests. So I decided to start a website myself. I called it Jooly's Joint.
Jooly's Joint is almost 12 years old now and has tens of thousands of members from all over the world. It is a huge blessing in my life, an enormous responsiblity and a privilege to be a part of.
Had I not gone through those miserable years of uncertainty about my diagnosis, then Jooly's Joint might never have been created.
I'm still not glad that I have MS. But I feel incredibly blessed to have been driven by MS to create Jooly's Joint.
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