Hi, I'm new here, its my third time recurrent of Her2 +, this time it spread to my lymph. I've got result by biopsy, So far I did just one CT scan last Friday, still waiting for next week ‘s doctor’s meeting to review the results. I've been booked to oncologist on early April.
I'm so worried the waiting time is too long, or is it normal?
When do you guys get the treatment started?
Hi FaithinGod and a very warm welcome to the online community which I hope you'll find is both an informative and supportive place to be.
I’m Anne, one of the Community Champions here on the Online Community and, although I'm not a member of this group, I noticed that your post hadn't had any replies yet. Responding to you will 'bump' it back to the top of the discussion list again.
While you're waiting for replies, it would be great if you could put something about your diagnosis and treatment to date into your profile as it really helps others when replying to you and also when looking for someone on a similar pathway. It also means that you don't have to keep repeating yourself. To do this click on your username and then select 'Profile'. You can amend it at any time and if you're not sure what to write you can take a look at mine by clicking on my username.
"Never regret a day in your life, good days give you happiness, bad days give you experience"
