Emotions and anxiety with a cancer diagnosis: How do you cope?
My emotions and anxiety along with ADHD since the diagnosis of cancer is extremely high.
I’m finding it hard to keep up with day to day stuff, not to mention all the treatments, etc.
What or how do we cope? I’m so tired and I still got to face radiation treatments. I go to counseling weekly and I’m ok a good part of the time. But I’m having trouble staying focused and emotionally charged all the time. Any suggestions?
Interested in more discussions like this? Go to the Cancer: Managing Symptoms Support Group.
I will be having my allogeneic transplant at Dana Farber Boston Mass. as an Out Patient and will have to relocate. My husband needs to be with me 24/7 for 100 days.
Thanks. I have been learning how to limit my time to think about cancer, appointments, insurance, finances, etc. If something requires immediate attention, I still limit the amount of time that I will spend on it. I’ll break it up and go for a walk. Also I’m learning to breathe in, the very minute my mind goes in a negative direction that will make me feel anxious or upset enough to cry. Before, I was crying so hard and so often that my eyes hurt. I was getting headaches and my eyes were twitching all the time. I had to stop! My counselor is helping me with ideas, like…to check myself several times a day. Then I breathe and imagine good things happening in my life now and in the future. It’s helping me.
Thanks for your input. I am getting better and stronger every day. I’m still at a standstill at times, but like you said I’m allowing myself grace and some time to find my way out of the storm when it hits, knowing it will come again. But knowing also that when it does come I’m going to find my way out in my own way and in my own time. I’m also relying on God to help me and he always does.
Thanks and God bless and keep us all in Jesus name.
Glenda.
Thank you so very much!
Hi @joannwkempel I’d like to add my welcome to Connect along with @alive. She and I, along with several others in the blood cancer support group have had stem cell transplants and are here to help you in any way we can.
I’d like to post a few links for you to get started. Actually, I’m going to cut and paste the exact discussion I recently posted with another new member about to have a SCT.
This is what I wrote to @marylou329:
I had an allogenic transplant as did @alive @edb1123 @kt2013 @jenmkr63 @timt347 and several other members. We’re all happy to share our experiences and answer any questions you might have.
Here are a few of our conversations:
My bone marrow transplant story; Will you share yours?
https://connect.mayoclinic.org/discussion/my-bone-marrow-transplant-bmt-story-will-you-share-yours/
~~~
Snapshots of life on the other side of transplant:
https://connect.mayoclinic.org/discussion/snapshots-of-hope-life-on-the-other-side-of-transplant/
All of us are in various stages post transplant. I’m coming up on 5 years so I’m about in the middle timeline of our group. Having a stem cell transplant offers us a second chance with life. It isn’t a guarantee because there can be risks and sometimes a relapse, as in Tim’s case. But it is worth the effort.
Where are you having your transplant? Will you have to relocate and stay in the clinic? Do you require a full time caregiver?
Joann, if you have leukemia, then I’m expecting you’ll be having an allogenic transplant, using donor cells? Would you like to share a little more about what type of cancer you have and how it’s being treated? Has there been a donor match for you?
Welcome @luciag. Cancer is overwhelming at many stages, be it new diagnosis, treatment or even after treatments are done. Can you tell me more about your cancer journey? What type of cancer do you have? Is this a new diagnosis?
I had an allogenic transplant, along with @alive @edb1123 @kt2013 @jenmkr63 @timt347 and several other members. We’re all happy to share our experiences and answer any questions you might have.
Here are a few of our conversations:
My bone marrow transplant story; Will you share yours?
https://connect.mayoclinic.org/discussion/my-bone-marrow-transplant-bmt-story-will-you-share-yours/
~~~
Snapshots of life on the other side of transplant:
https://connect.mayoclinic.org/discussion/snapshots-of-hope-life-on-the-other-side-of-transplant/
All of us are in various stages post transplant. I’m coming up on 5 years so I’m about in the middle timeline of our group. Having a stem cell transplant offers us a second chance with life. It isn’t a guarantee because there can be risks and sometimes a relapse, as in Tim’s case. But it is worth the effort.
Where are you having your transplant? Will you have to relocate and stay in the clinic? Do you require a full time caregiver?
I will be having an Allogenic transplant from a Donor. I would love to be connected with someone who has been through it. Thank you for your quick response.
Hi @marylou329 I’m here to help you through that stem cell transplant. There are several of us who have had either Allogenic transplants using donor cells or autogenic transplants using their own cells. I’d love to get you “connected” with the right new friends to hold your hand along your new path.
What type of transplant are you having?
I am facing a stem cell transplant in a couple of months as well. I am very nervous and I know it won't be easy, but I have God on my side. I try to surrender my sickness to God and know that He will take care of everything. Some days are easier than others.
Thank you @alive. I’d like to get your views on the process.