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A MyMyelomaTeam Member asked a question 💭
want to share a little update about my journey. Recently I went for a CT scan of my lungs, and today the doctor explained the results to me. They found some changes in my left lung compared to before. There are areas where the lung lining looks thicker, and a small mass in the lower part of the left lung has grown a bit since my last scan. Because of these changes, the doctors want to do another test called a bronchoscopy, where they use a small camera to look inside the airways and take samples to understand it better. Hearing all this was not easy for me. It made me emotional because it feels like one thing after another. But at the same time, I am thankful that I am already under medical care and the doctors are taking steps to find out exactly what

Can members tell the difference symptoms or side affects that usually happen to you up till now
Like me side effects always my foot feel cold, neck pain comes and goes
But l don’t have back pain or anything like before.fatigue,body pain no sleep problem and shingles

November 21, 2025
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A MyMyelomaTeam Member

My biggest issues are fatigue and memory problems.

November 21, 2025
A MyMyelomaTeam Member

@A MyMyelomaTeam Member Donna is right, you are dealing with a lot. I’m lucky in that respect. My wife is wonderful and supportive. So is my son. They go out of their way to help me. Most of my friends and extended family have been supportive and helpful. My oncologist/hematologist has increased the testing regimen, and referring me to other specialists as required. They can see how I’ve deteriorated over the years.

November 23, 2025 (edited)
A MyMyelomaTeam Member

I am sorry Angie I had no words of encouragement for you to say but you are the special to replace the fears uncertainty and doubt of a new diagnosis with confidence and trust
Dealing with fear
God bless you AngieNixon
You are not alone

November 25, 2025
A MyMyelomaTeam Member

Oh Robert. I'm so sorry you have so much to deal with. I've been on treatment 8 years also. Big hugs your way. It's so hard to deal with the uncertainty. 🥺

November 22, 2025
A MyMyelomaTeam Member

Fatigue, memory fog, and neuropathy

November 22, 2025

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