It seems like a lot of people on here are using LDN and having at least some success with it. I've read a bit about it and am feeling interested and hopeful.
I asked my GI about it at my last appointment, and he hadn't heard of it. That felt a little discouraging.
What were your experiences like talking to doctors about LDN? Were they familiar with it? Who prescribed it? Did it take convincing, or were they confident about it?
I've been on Entocort since my diagnosis last month, and it has been working well so far, but it is likely to continue to work for a year at the most...so I want to have as much information as I can and know my options when I need to make a change in my treatment.
I asked my GI about it at my last appointment, and he hadn't heard of it. That felt a little discouraging.
What were your experiences like talking to doctors about LDN? Were they familiar with it? Who prescribed it? Did it take convincing, or were they confident about it?
I've been on Entocort since my diagnosis last month, and it has been working well so far, but it is likely to continue to work for a year at the most...so I want to have as much information as I can and know my options when I need to make a change in my treatment.