1. < Blood Cancers & Disorders

Non Hodgkin's Lymphoma- Watch & Wait Approach

Posted by Jackie, Alumna Mentor @travelgirl, Jun 15, 2018

I would like to meet others who were diagnosed with a lymphoma and are on watch and wait treatment.

I have been on a watch and wait lymphoma watch now for 2 1/2 years. I currently get blood work done every 6 months and a CT Scan once a year.
Has or is anyone else having the cancer monitored like this? Are there people who lived their whole life without ever getting treated for lymphoma?
Would love if we could share our progress on here.
Jackie

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

Moderator
Colleen Young, Connect Director | @colleenyoung | Oct 31, 2018
In reply to @bordercolliecra "Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had..." + (show)
@bordercolliecra

Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had to start treatment as I was stage 3 as my GP had said I was having an early menopause - I was 46 at the time). I had 5 rounds of FMD as Rituximab was too expensive then. I went into molecular remission. In 2011 a lump came up on my head. My GP said it was a cyst but it grew so large I was referred to the Sarcoma specialist. Long story short it was extra nodal NHL. I had bendamustine first but the tumour regrew and I had radiotherapy. Two years ago I started with abdominal pain and only a slightly enlarged spleen was obvious on an ultrasound. I was diagnosed with IBS!! Forward to this August and I started having pains in my left side and between my shoulders. A new GP sent me for an ultrasound which showed a Splenic Cyst and slightly enlarged liver. I have also had a colonoscopy and that was clear. Hopefully I will get answers after the CT scan and seeing my Haematologist next week.

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Hi @bordercolliecra, you can copy and paste your message to this discussion:
- Non Hodgkin's lymphoma https://connect.mayoclinic.org/discussion/non-hodgkins-lymphoma-2c0eb7/

Once you've done that I can delete it from this discussion. Although, @travelgirl is right. It's okay here too.

REPLY
Jackie, Alumna Mentor | @travelgirl | Oct 31, 2018
In reply to @bordercolliecra "How can I delete my posts as I put it on the wrong board. It shouldn't..." + (show)
@bordercolliecra

How can I delete my posts as I put it on the wrong board. It shouldn't be on Watch and Wait?

Jump to this post

@bordercolliecra I think it is fine being posted here. But I will tag Colleen and she can make the final call @colleenyoung

REPLY
Jackie, Alumna Mentor | @travelgirl | Oct 31, 2018
In reply to @bordercolliecra "Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had..." + (show)
@bordercolliecra

Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had to start treatment as I was stage 3 as my GP had said I was having an early menopause - I was 46 at the time). I had 5 rounds of FMD as Rituximab was too expensive then. I went into molecular remission. In 2011 a lump came up on my head. My GP said it was a cyst but it grew so large I was referred to the Sarcoma specialist. Long story short it was extra nodal NHL. I had bendamustine first but the tumour regrew and I had radiotherapy. Two years ago I started with abdominal pain and only a slightly enlarged spleen was obvious on an ultrasound. I was diagnosed with IBS!! Forward to this August and I started having pains in my left side and between my shoulders. A new GP sent me for an ultrasound which showed a Splenic Cyst and slightly enlarged liver. I have also had a colonoscopy and that was clear. Hopefully I will get answers after the CT scan and seeing my Haematologist next week.

Jump to this post

This is fine here.. I think it's ok?

REPLY
bordercolliecra | @bordercolliecra | Oct 31, 2018
In reply to @bordercolliecra "Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had..." + (show)
@bordercolliecra

Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had to start treatment as I was stage 3 as my GP had said I was having an early menopause - I was 46 at the time). I had 5 rounds of FMD as Rituximab was too expensive then. I went into molecular remission. In 2011 a lump came up on my head. My GP said it was a cyst but it grew so large I was referred to the Sarcoma specialist. Long story short it was extra nodal NHL. I had bendamustine first but the tumour regrew and I had radiotherapy. Two years ago I started with abdominal pain and only a slightly enlarged spleen was obvious on an ultrasound. I was diagnosed with IBS!! Forward to this August and I started having pains in my left side and between my shoulders. A new GP sent me for an ultrasound which showed a Splenic Cyst and slightly enlarged liver. I have also had a colonoscopy and that was clear. Hopefully I will get answers after the CT scan and seeing my Haematologist next week.

Jump to this post

How can I delete my posts as I put it on the wrong board. It shouldn't be on Watch and Wait?

REPLY
1 reply
bordercolliecra | @bordercolliecra | Oct 30, 2018

Hi. I am in England. I was diagnosed with Follicular NHL in August 2000. I had to start treatment as I was stage 3 as my GP had said I was having an early menopause - I was 46 at the time). I had 5 rounds of FMD as Rituximab was too expensive then. I went into molecular remission. In 2011 a lump came up on my head. My GP said it was a cyst but it grew so large I was referred to the Sarcoma specialist. Long story short it was extra nodal NHL. I had bendamustine first but the tumour regrew and I had radiotherapy. Two years ago I started with abdominal pain and only a slightly enlarged spleen was obvious on an ultrasound. I was diagnosed with IBS!! Forward to this August and I started having pains in my left side and between my shoulders. A new GP sent me for an ultrasound which showed a Splenic Cyst and slightly enlarged liver. I have also had a colonoscopy and that was clear. Hopefully I will get answers after the CT scan and seeing my Haematologist next week.

REPLY
3 replies
vonbaron36 | @vonbaron36 | Oct 23, 2018
In reply to @travelgirl "@susanlim Welcome to connect @vonbaron36 Do either of you take Vitamin C ? When I was..." + (show)
@travelgirl

@susanlim Welcome to connect @vonbaron36 Do either of you take Vitamin C ? When I was first diagnosed and my lymph nodes were enlarges I started taking that. Vitamin C is good immune booster. One food I ate regularly was Sweet potatoes that has some good vitamins to help boost our recovery. Lots of lean proteins. My lymph nodes shrunk by themselves and with NHL they do go up and down in size. I was told by my Dr that Radiation and chemo does not cure or extend a persons life with NHL. They found a watch and wait to more effective since the lymph nodes are known to go up and down in size. Exercise helps us. Which I have trouble staying consistent with. Read about Vitamin C and ask your Dr about trying to take a larger dose will benefit you?

I wish you the best Jackie

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No I didn't take vitamin C. In fact I don't take any vitamins.

REPLY
susanlim | @susanlim | Oct 23, 2018
In reply to @travelgirl "@susanlim Welcome to connect @vonbaron36 Do either of you take Vitamin C ? When I was..." + (show)
@travelgirl

@susanlim Welcome to connect @vonbaron36 Do either of you take Vitamin C ? When I was first diagnosed and my lymph nodes were enlarges I started taking that. Vitamin C is good immune booster. One food I ate regularly was Sweet potatoes that has some good vitamins to help boost our recovery. Lots of lean proteins. My lymph nodes shrunk by themselves and with NHL they do go up and down in size. I was told by my Dr that Radiation and chemo does not cure or extend a persons life with NHL. They found a watch and wait to more effective since the lymph nodes are known to go up and down in size. Exercise helps us. Which I have trouble staying consistent with. Read about Vitamin C and ask your Dr about trying to take a larger dose will benefit you?

I wish you the best Jackie

Jump to this post

Thanks!

REPLY
Jackie, Alumna Mentor | @travelgirl | Oct 23, 2018

@susanlim Welcome to connect @vonbaron36 Do either of you take Vitamin C ? When I was first diagnosed and my lymph nodes were enlarges I started taking that. Vitamin C is good immune booster. One food I ate regularly was Sweet potatoes that has some good vitamins to help boost our recovery. Lots of lean proteins. My lymph nodes shrunk by themselves and with NHL they do go up and down in size. I was told by my Dr that Radiation and chemo does not cure or extend a persons life with NHL. They found a watch and wait to more effective since the lymph nodes are known to go up and down in size. Exercise helps us. Which I have trouble staying consistent with. Read about Vitamin C and ask your Dr about trying to take a larger dose will benefit you?

I wish you the best Jackie

REPLY
2 replies
susanlim | @susanlim | Oct 23, 2018
In reply to @susanlim "Thank you! About the same. I hope it helps, but I figure it cannot hurt. Wishing..." + (show)
@susanlim

Thank you! About the same. I hope it helps, but I figure it cannot hurt. Wishing you continued good health.

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They would not consider radiation for me because possible region too big (neck and both armpits). So watch and wait.

REPLY
susanlim | @susanlim | Oct 23, 2018
In reply to @vonbaron36 "Also my curcumin has BioPerine for absorbtion. And I use pepper on my eggs also." + (show)
@vonbaron36

Also my curcumin has BioPerine for absorbtion. And I use pepper on my eggs also.

Jump to this post

Thank you! About the same. I hope it helps, but I figure it cannot hurt. Wishing you continued good health.

REPLY
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