Hello! Does anyone have any knowledge if cll is covered by the recent govt / health dept. Advice to stay home? Thank you...
Thank you for your replies. I am already shielding but I'm trying to get my partner's employer to understand that he also shouldn't be working. Would be easier if I had a text/letter from the NHS but not received it yet. At least I can now tell them that CLL is definitely one of the criteria for shielding.
Hi all,
If anyone hasn't heard either by letter or text by Sunday, you can register here:https://www.gov.uk/coronavirus-extremely-vulnerable
or you can do it right now if you wish.
Best wishes to all, stay safe and be well,
Mike
Hi everyone, thank you all... It truly is a frightening time, I feel so helpless... I've still not heard anything, although my boss did a risk assessment on me today, she didn't think I would have to stay home as, "you're pretty low down the list of cancers" as I've not had treatment etc!!! I explained about my immune system being pretty poor, lymphocytes basically shot... and she did the head tilt and shrugged shoulders... Ah well! Stay safe my lovelies, big virtual hugs to each and everyone of you xxx
Sal, unfortunately your boss needs to understand that you are ‘way up’ in the governments extremely vulnerable group.
Just ask them to look at the Governments Information
You need your look after yourself
People falling into this extremely vulnerable group include:
Solid organ transplant recipients.
I'm being shielded at work, by not being put on the front line, but as information is changing so often, we're all playing a bit of catch up! Does it sound bad to say I'm waiting for the text or letter to take the decision out of my hands..? Thanks Mike et Al, responses very much appreciated. S
Government Information for us all.
COVID-19: guidance on shielding and protecting people defined on medical grounds as extremely vulnerable
Information for shielding and protecting people defined on medical grounds as extremely vulnerable from COVID-19.
Dick
It’s important to remember that once you have been diagnosed with a blood cancer you are living with a blood cancer.
I was basically on W&W for 14 years for my type of NHL and I was still classed as having full on blood cancer. During my W&W it was coming and going then a trigger (virus I was told) set it off so went into full on treatment.
I have been in remission for 3 1/2 years now and my team did say that they just don’t know what this new virus will do to any dormant cancer cells that my immune system is ‘just’ keeping under control - so doing my best to keep it at a safe distance.
Hiya all
I was diagnosed with CLL about three years ago and am on watch and wait and probably like many others I haven’t received any communications D from anyone to confirm the latest instruction for high risk persons
i have a daughter who has gastroparesis and is on tpn six days s week as well as a pej drain tube
She received a text last Monday and has received several communications since
I am assuming therefore that if I am on the high risk then I would have received something by now
The guidelines are very clear that anyone with a blood cancer is regarded as extremely vulnerable. Being on watch and wait doesn't negate that.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007