I was diagnosed on 01/07 with multiple myeloma. I am just awaiting my treatment dates but have had biopsy, mri and ct scan. I’m due to have chemo and then a stem cell transplant
I am still at the blubbering stage. I can’t speak to anyone about it without crying. I know it will get better, and so will I. It’s the feeling of not being in control. I’m so used to being the organiser etc and I have no say in this phase of my journey. Im very anxious, angry, sad etc. All normal in this situation I believe.
I’ll be looking for “tips” once I start the treatment, so for now, stay safe all.
Hi. Please lean on us. We have all been there Of course so much to take in FYI. I am 17 months post stem cell transplant. You will need to let others do some helping It’s a joney worth taking g even now new treatments are come available. Incredible research. All the tests will guide your care team on what course to take. There are so many helpful guide’s In
acmillan website. We can help and guide from our own experiences. I am living a good life. A new normal. I drive walk. Ride a bike ( which is great because I couldn’t before !). Walk the dog I am retired but still work remotely, It will not control you ! You will control it ! Kevin
Hi Teresa
Welcome to the forum.
I went through the blubbering phase too. To be diagnosed with cancer - let alone one which is incurable - can be pretty traumatic.
Vespa has mentioned the resources on the Macmillan website. Also, the charity Myeloma UK has a peer buddy service, where you can talk with someone who has had myeloma for a while:
Some people can derive support from religion. Personally, I meditate to calm my thoughts.
You say that you feel out of control. That was roughly how I felt at diagnosis in 2022. I can suggest a couple of things from my experience.
- Know your enemy. I read up on myeloma and in particular treatments. I have learnt a whole new vocabulary of t(4, 14), bispecific antibodies, CAR-T and a lot more! You would then be able to have more meaningful discussions with your doctor, know what each chemo drug does etc. We can of course help with the learning process.
- You are largely in control of your lifestyle. I exercise hard (though I couldn't do much until remission), eat healthily, don't smoke and barely drink.
- I planned beyond the 6 months of treatment, deciding where I would want to go on holiday. There is light at the end of the tunnel - focussing on being in control then can help.
People live long lives with myeloma these days!
Chicken2 (over 2 years in remission and enjoying life).
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
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