← Return to Treatment for NHL: Rituximab & Bendamustine

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@JustinMcClanahan

It is important to remember our differences here on Connect. Each member brings their own experiences, background, beliefs, and knowledge to Connect and more often than not, that is the strength of a diverse community. However, it is good to keep the Community Guidelines (https://connect.mayoclinic.org/page/about-connect/tab/community-guidelines/) in mind when posting.

In particular, Section 2 states:
- Be inclusive. Not everyone shares the same religious or political beliefs. Don't impose your beliefs on others.
- Exercise tolerance and respect toward other participants whose views may differ from your own. Disagreements are fine, but mutual respect is a must.

Back to Non-Hodgkin's Lymphoma and Rituxan treatments. @susanlim, you had mentioned in another discussion that you were still in the wait and watch phase, is this still true or are you potentially facing Rituxan or another treatment? @quiteachiver75, if you are comfortable sharing, have you been diagnosed with NHL as well?

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Replies to "It is important to remember our differences here on Connect. Each member brings their own experiences,..."

Thank you. Agreed.

I am still on watch and wait. A question I had for the group is why do you all seem to have annual CT scans? My doctor is fully opposed to this, saying it subjects the body to unnecessary radiation. The basic protocol I am living with is that in the absence of symptoms or difficult or stigmatizing tumors, that we do nothing except periodic check ups and blood work. I’d be interested in hearing the reasoning behind the annual cat scans.