Mantle cell lymphoma

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 I have been told im in remission. I have had 6 lots of R-CHOP. Now i need 2 years of 8 weekly rituxamab. Any one know what the side effects of this will be. I feel like ive been unwell for 7 months .  

  • Hi   and warm very welcome to the Macmillan Community although I am sorry that you had to find us and especially sorry to hear about your Lymphoma journey thus far.

    I am Mike and I help out around our Lymphoma groups. 

    I don’t have Mantle cell lymphoma but I was diagnosed way back in 1999 at 43 with a rare (8 in a million) incurable but treatable type of Cutaneous T-Cell NHL (a type of slow growing Low-grade non-Hodgkin lymphoma)……. eventually reaching Stage 4a in late 2013 when a second, also rare (4 in a million) type of aggressive Peripheral T-Cell NHL (a type of fast growing High-grade non-Hodgkin lymphoma) took me to stage 4 so although my Lymphoma ‘type’ my be different I most definitely appreciate the challenges of this journey rather well.

    We actually have a dedicated Mantel Cell Lymphoma support group.

    This group is a safe places to talk to others with a similar diagnosis, treatment experience, to ask questions and get support.

    Click on the link above……. and when the group page opens you will see a [Black - Click to Join - Banner] at the bottom of the page, click in this box and this will then confirm that you have joined the group.

    When you are ready……. you can introduce yourself by putting up your very own post by clicking [+ Create new post] or [+] in the top right of the group page.

    You can copy and paste the text from this post into your new post.

    I will keep an eye open for you but if you are not sure what type you have pleased do get back to me on this post and I will help you out further.

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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