In retrospect I wish I had kept a diary of what was happening, the dates and the drugs etc I was given. If you are newly diagnosed then I suggest you do this - because you are so sick your memory is not so good so it's good if it's written down. I suggest that if you have a partner then it is useful for them to be at appointments to begin with - you often hear different things from the Doc and it helps your partner to understand it all.


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I hope you've had a chance by now to read through the forum as it will give you a pretty good sense of how broad the question of treatment for this disease is, for example, and how we- family and weggie alike- have to come to grips with the fact that you can get better with proper treatment, but there is no cure. You can go into remission, but there is no guarantee you won't have a flare later down the road. While that sounds grim, I'd say we weggies on this forum have pretty good attitudes about our disease. Also, I hope we can help you formulate questions for you and your mother to pose to her doctors. We are in this together.

