Want to connect with others with Splenic B cell Marginal Zone Lymphoma

Posted by April @sabtahis, Jul 24, 2016

There are over 80 different subtypes of lymphoma . This is a slow growing lymphoma.I'd like to know and communicate with any patient if possible.

Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.

@scsimpson

I was diagnosed in May with splenic marginal zone lymphoma. For the past 6 years I have been dealing with Itp. Now it turns out that it was smzl.I had my spleen removed in July. Now I am waiting until April to have another bone marrow biopsie to see if the lymphoma in my marrow go down. Does anyone have any advice?

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Lori,

Yes this will be my first bone marrow biopsy and I appreciate your advice. I will definitely opt for lala land and snacks! Thx. R

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@reneemp

Laurie,

I am wondering if you have found information about how to be proactive with SMZL? I am 58 and recently diagnosed. Waiting for bone marrow biopsy. Thanks. Renee

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Hi Renee, being a veteran of bone marrow biopsies with more than 13 ‘under my belt’ so far. 3 were without anesthesia, the other 10 were in la la land of a mild sedative, which I highly recommend!
It’s the same sedative given for a colonoscopy. You’re under 10 minutes tops and then wake up oblivious to the procedure. At Mayo, I wake up to Lorna Doone’s and Juice. ☺️

If the procedure will be done in a facility where sedation isn’t offered have your NP get you a prescription for lorazapam. A small dose of 1mg or 1.5 mg a half hour before the procedure will help relax you.
You’ll have a local anesthetic injected in the area which will help numb the site of the aspiration.

If I’m having it without anesthesia, I ask one of the nurses to keep engaged in conversation for distraction. That helps quite a bit. The procedure doesn’t take long and usually the sample area feels just a little bruised for the next day or so.

Is this your first biopsy?

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@scsimpson

I was diagnosed in May with splenic marginal zone lymphoma. For the past 6 years I have been dealing with Itp. Now it turns out that it was smzl.I had my spleen removed in July. Now I am waiting until April to have another bone marrow biopsie to see if the lymphoma in my marrow go down. Does anyone have any advice?

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Laurie,

Thanks for getting back to me. I agree about the challenges about being good - healthy diet and exercise. The most challenging thing for me is the fatigue. I use to be much more active and it’s exhausting being tired.

I am a breast cancer survivor so I already am working hard at being healthy. I do admit last night I had some sweet potato chips - yummy!

Thanks for the bone marrow info. Clearly something I am not looking forward too.

Yes, continuing to connect would be nice.

It’s getting cold in Minnesota. Enjoy the day. Renee

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@scsimpson

I was diagnosed in May with splenic marginal zone lymphoma. For the past 6 years I have been dealing with Itp. Now it turns out that it was smzl.I had my spleen removed in July. Now I am waiting until April to have another bone marrow biopsie to see if the lymphoma in my marrow go down. Does anyone have any advice?

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Hello Renee! I love your question and even though I have not found a great deal of research due to the rarity of SMZL, I have discovered that regular exercise and a whole diet have helped. I am also a diabetic, for which I have my A1c tested every nine months. A1c is an average blood glucose reading over a three month span. Those 3 months prior to each test, I am fastidious about my exercise and diet. This last time, my SMZL bloodwork was at the same time. My results for each appointment showed excellent numbers. I do not think it's a coincidence.

That being said - I don't think there is magic to being proactive - but it is challenging to always be "good."

Good luck with the bone marrow biopsy. I had an excellent team (there were 4 or 5 people in the room) with one person at my head whose job was to keep me comfortable. You'll walk out of the procedure but there is discomfort - just wanted you to be prepared.

I would really love to continue talking with you - since SMZL is usually a "wait and watch" condition - it can be frustrating to do just thatt and I rarely find people who want to talk about it!
Laurie

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@kayak4me

My name is Laurie and I was diagnosed almost 2 years ago with SMZL after routine bloodwork for an ortho procedure. I wasn’t officially diagnosed until after a bone marrow biopsy. I am extremely lucky to have been diagnosed early, and quarterly bloodwork find me remaining pretty stable. I am 64 years old and fairly active.

Has anyone seen or heard about healthy lifestyle models for SMZL patients? There isn’t a lot of research because we’re so rare, but I’d like to be as proactive as possible and find resources on diet, exercise, and mindfulness as it pertains to the immune system. So happy to have found a current group!

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Laurie,

I am wondering if you have found information about how to be proactive with SMZL? I am 58 and recently diagnosed. Waiting for bone marrow biopsy. Thanks. Renee

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@cdwilm27

Stan, I do get weekly labs drawn. My H&H went from 10.4 and 32.8 on 10/20 to 11.3 and 35.2 on 10/27. My lowest labs were week 1 when I was 9.9 and 32 on 10/4.

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cdwilm27, Hello, Is nice to see your labs are showing improvement and hope they continue. I think you have finished your infusions and wondering if they will monitor your progress or if other treatments are being considered. ?
The spot in my lung is small, 7 mm, but PET showed activity. I have follow up appointments to determine what is the best course of action. Will look around Mayo connect to see there are other threads that I can also join.
PET did not show any SMZL related issues, other than a spleen measurement increase of 1 cm over the past year.

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Stan, I do get weekly labs drawn. My H&H went from 10.4 and 32.8 on 10/20 to 11.3 and 35.2 on 10/27. My lowest labs were week 1 when I was 9.9 and 32 on 10/4.

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Stan, I will be praying that the spot on your lungs is benign.

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@cdwilm27

So Stan did see my reply from today?

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cdwilm27, Yes, I think I received all the messages. I thought I acknowledged this yesterday, but must not have hit reply because I don't see it posted. Thanks and please stay in touch.

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Yesterday's Rituximab infusion went well. The nurse was able to increase the rate of drops per minute as my body has now accepted this med and no longer causes the reaction I had when first infused. I was out in 2.5 hours. I did have the fatigue that I normally experience after my infusion. Today I feel good. Next Thursday is supposed to be my last infusion. I will meet with the doctor before and discuss my treatment plan. Happy Halloween Friday!

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