I’ve posted a few times about finding a doctor, finding the right doctor, when it’s time to find a new doctor and so on. You see, if you have had carcinoid cancer / neuroendocrine cancer for any length of time now then you know that finding a doctor that can help you is quite difficult. Just in case you haven’t read any of those posts here’s is a great post from LucysNoidBlog that you will find helpful. Here’s a blurb from the article.
Somewhere in the US, a patient with neuroendocrine cancer is searching for another doctor – someone who offers appropriate treatment or can at least explain what is happening; what to expect, what can or can’t be done. The patient is fed up with doctors who either don’t know enough to treat them or haven’t bothered to stay current on new treatment options. The patient may not know how to find another doctor but they know one thing for sure – the doctor they have is not going to help them cope (much less beat) this cancer. Read More
As soon as I’ve finished going through my old posts and linking to relevant “stuff to get” items then I will be “hitting the links!” Sorry for the bad pun, but the plan is to update my links section and I will be linking to LucysNoidBlog and a few others that I have found. In the mean time, take a look at her blog if you haven’t already. It’s very informative.