Another newby : Hi I’m reading about CLL but mine... - MPN Voice

MPN Voice

10,886 members15,202 posts

Another newby

Brendaf profile image
7 Replies

Hi I’m reading about CLL but mine is CNL does anyone else have this diagnosis? Apparently I’m only one of five in the country with this very rare blood disorder.

Written by
Brendaf profile image
Brendaf
To view profiles and participate in discussions please or .
7 Replies
stillkicking profile image
stillkicking

Hi Brendaf,

Welcome to the forum. I had not heard of CNL before, so have consulted "Dr Google" and had a read about it. I see what you mean by "rare"... it certainly is! I see that it also is part of the MPN family and that, in the case of CNL it is the neutrophils that are proliferating.

It must be a very lonely thing having a condition as rare as yours and I do hope that, ideally, you do find others with the same condition who can offer help and guidance. Whilst most of us here have other MPNs and are probably busy making too many platelets or red blood cells rather than neutrophils, I know that we do battle with loneliness, fear, fatigue, feeling unwell, "experts" in white coats who don't understand us, experts we find hard to understand, and so on, and I am sure you will find a great deal of support and a warm welcome here.

Kind Thoughts to you,

Peter

Brendaf profile image
Brendaf in reply tostillkicking

Thank you Peter I have been reading all about MPNs but they didn’t really apply to my condition. I’m under the care of Professor Harrison who is keeping an eye on me and it’s just a matter of wait and see which is not ideal but at least she has the knowledge and expertise. Thanks again. Brenda

stillkicking profile image
stillkicking in reply toBrendaf

Hi Brenda,

Pleased to see that you have Prof H keeping an eye on things, but it must be a difficult time for you. I'm guessing that you were only recently diagnosed?

Best wishes, Peter

Ebot profile image
Ebot

Hi Brenda. Well you make the rest of us MPNers look entirely common! I can offer nothing helpful except to say I would take great heart from being under the care Prof H and the team at Guy’s. You are in excellent hands. Always a comfort to have faith in your clinical practitioners. All the best. Keep us posted.

Brendaf profile image
Brendaf in reply toEbot

Hi Ebot thank you for your reply and yes I’m happy to have expertise from Guys hospital. I will keep you all informed if I find any further information. Brenda

Wyebird profile image
Wyebird

Wow you are a rareity, I’ve had to google this. I do hope you get the support you need both medically and emotionally. Welcome to this forum - my life line.

Brendaf profile image
Brendaf in reply toWyebird

Hi Wyebitd thank you for your reply I’m hoping to find someone else with this rare condition but it’s nice to have people with similar conditions who understands what it’s like. Brenda

Not what you're looking for?

You may also like...

Newby

Hi I'm new to this having had my diagnosis of Polycythemia Rubi Vera PV confirmed a week ago. Has...
Hilarya profile image

Hello from a newby!

Hi all Thought I’d introduce myself. I’ve read a lot of your posts and find you all a mine of...

another booster.?

does anyone know if and when we will get another covid booster this year , I’m sure I read that...
sweetpea19 profile image

Newby to ET

Recently been diagnosed with ET. Consultant suggesting Chemo Pill, but only after "going through...
StigerP profile image

Let’s help one another

Hi, I wrote this poem already in another thread but wanted to share it with you all in the hope it...
Aime profile image

Moderation team

Debinha profile image
DebinhaAdministrator
Mazcd profile image
MazcdPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.