Facing Cancer Recurrence, PTSD & Acknowledging Mental Health
It's extremely difficult to face the fact of recurring cancers. After treatments we try and get away from it all and live our life. Then along comes another CT scan or PET scan and POW, you have to face another cancer. My reaction was developing PTSD.
You can read what I wrote in my blog: https://my20yearscancer.com/blog/
How do we cope? How do we react? What do we do?
How have you all reacted to another cancer? Or the possibility of another one? Has your "already compromised" mental health been able to deal with it? How? Or not?
Interested in more discussions like this? Go to the Cancer: Managing Symptoms Support Group.
@sakota- I am on the east coast and go to MGH. One big fear with cancers is that "doctors wont get it all". I think that this is a legitimate fear. Legitimate because it sometimes happens. Sometimes doctors can't remove the entire cancer. Sometimes radiologists miss a tumor altogether. This happened to me.
With this, we have to deal/work with what we get. It's not perfect, it's not ideal, but all we have are humans to make decisions and act.
I did merry but I am beginning
To regret that decision. I changed to dealing with drs here and I just don’t feel right about what they say. My biggest fear is that they will miss sometthing and then it will be too late. Do you go to mayo at Rochester. Maybe sometime we can schedule at the same time. Right now I’m waiting to hear for appt with pulmonologist in February Keep the faith and the power
Sakota, I continue to travel 9 hours each way to have all my follow ups done at the Mayo Clinic in Rochester. After the beginning of my journey I feel they are the only ones I want to deal with concerning my cancer. I have a primary physician here but all my cancer treatment is done at Mayo. Please consider this if you can.
Sakota- Did you move away from Mayo? If you are uncertain or do not feel right about a doctor then get a second opinion. I am so glad that you are stable now! When do you go back for another scan?
@merry and Linda. Thanks for the wishes. And yes I did get a stable report. But you know what I don’t know if I trust the dr here. I was with the drs at mayo and trusted so much the surgeon and radiologist. It almost sounds like this dr is saying ok you been stable a year maybe you are in the clear but I know that’s not right. This about the dr here is probably my imagination.but yet I don’t feel right about the stable thing and he is missing something. Thanks again sveryone
Sakota- Fingers crossed for you! Let us know.
Sakota-thinking of you today and hoping you receive stable results.
@linda 10- lol. Supposedly multifocal adenocarcinoma is not that uncommon. Wonder where everyone is...
Unfortunately I don't know anyone else with multifocal adenocarcinoma. I feel very fortunate that there are at least 3 of us here.
@linda10 and @sakota. I was going to introduce the two of you tomorrow morning. I'm glad that you have met. Maybe we can grow our group by bringing in others who also have multifocal adenocarcinoma. If you know of anyone invite them to join us!