I have had me NETS for 15 years and it is a very rare complex and nasty cancer that is not easy to detect and is found in many countries.

As i say i have 15 years of a mass of experience including many reatments.

If i can be oo assistance to anyone please let me know?

My first bit of information is that if you have not got access to a NET doctor and if your GP can do it then get onto it straight away as these Onchologists are the best people to deal with this cancer.

Finally, NEUROENDOCRINE UK site on line.

All the best

Andy