Mandy's Myeloma Journey

  • Home
  • Mandy's Myeloma Journey

Mandy's  Myeloma Journey Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Mandy's Myeloma Journey, Hospital, .

This page was created to put my journey of treatment for Multiple Myeloma and it takes it away from my normal page if people don't want to know about it.

My bloods are pristine apparently, phew! 😁Here's to another 6 months in remission 🤞
03/12/2022

My bloods are pristine apparently, phew! 😁
Here's to another 6 months in remission 🤞

21/11/2022
17/05/2022

Consultant advised me today that the bloods look good and I'm still in remission 😁
One result still to come from Southampton, but he thinks they will be okay 🤞
Echo cardiogram also returned good results and all is looking and working as it should ❤️
www.myeloma.org.uk

Send a message to learn more

20/12/2021

Our NHS is brilliant.
Today, I received details that I am eligible for the new pill Lageviro to reduce the effects of covid if caught.
They are sending a PCR test kit so immediate action can be taken if I start to develop symptoms.
Amazing service, just amazing.
👏👏👏😷😷😷👏👏👏

17/11/2021

Consultant appointment today:
No trace of paraproteins (cancer) 😁
Light chains are good, liver and kidney function is normal.
STILL IN REMISSION, but thinking of those that aren't 😔

23/05/2021

So just a quick update:
both vaccines now received and I had my 6 month consultant appointment this week results are that my bloods are clear of any para proteins (cancer) and it looks clear and healthy.

23/04/2021

If you know anyone diagnosed with a blood cancer: Leukaemia, Lymphoma or Myeloma, advise them to contact their GP, so that the rest of the household can be vaccinated.
My 2 boys, 22 & 20 have just booked their appointments for their vaccine.
Keep going NHS, you are still doing a fantastic job.
💉😷💉🤗💉😷💉🙂💉😷💉😀💉

18/11/2020

6 month review today and the Consultant advises that bloods and kidneys are looking good, with no trace of Myeloma. 🙂
Still waiting on one result from Portsmouth but he is confident these will be okay. 🤞
Consultant advises that if he was looking at my bloods, not knowing that I'd had a alot of treatment (chemo, steroids, thalidomide etc) and a stem cell transplant, he would be unaware of my treatment history as the bloods are looking normal - get me!!! 😉

The reality of being in remission - interesting that Jo mentions PTSD!
18/08/2020

The reality of being in remission - interesting that Jo mentions PTSD!

After finally making it to the end of her blood cancer treatment, Joanna entered an anxiety-ridden world. She explains how she's overcoming some of these struggles, so that she can give her second chance at life its best shot.

This is the steroid I took, with thalidomide, other tablets and chemo, to rid the paraproteins (cancer) from my blood, b...
16/06/2020

This is the steroid I took, with thalidomide, other tablets and chemo, to rid the paraproteins (cancer) from my blood, before the stem cell transplant!🌈
They thought there would be something already in use to help with the fight against covid-19.😀
Fingers crossed they now find a vaccine and I can go back to work and shopping again.💉
Stay safe 😘

The drug, dexamethasone, reduced death rates by a third for patients on ventilators, and by a fifth for patients needing oxygen.

Address


Website

Alerts

Be the first to know and let us send you an email when Mandy's Myeloma Journey posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Mandy's Myeloma Journey:

  • Want your practice to be the top-listed Clinic?

Share