New member

[kevinbros]

Good evening

I am new to this site as of yesterday.Diagnosed with myleofibrosis August last year.Currently being treated at UCLH.

[Mrs_Average]

Hi kevinbros

Welcome to the site. Sorry to hear about your diagnosis. I had the same diagnosis last August too. It's a lot to take in. Check out the information on the MPN Voice site and I you'll find many of us on the site have similar experiences.

All the best

[jane13]

hi, u r at a good place for treatment.

[mhos61]

Hi Kevinbros, I would just like to welcome you to the forum, you've made a good decision in joining.

Mary x

[Lainy1]

Hello and welcome,

Sorry to hear about your diagnosis.

This is an amazing site for information and we all support each other through tough times.

Best wishes lainy

[MFBMT2011]

Welcome. Brilliant hospital. Had my stem cell transplant for MF there several years ago. Please share more about you and your diagnosis and current treatment and ask any questions you may have so people can try and help. Chris

[Rachelthepotter]

Hi Kevinbros

Welcome. i had an MF diagnosis in January this year. (2017) and the people on this site have been a huge help. Best regards

[funnyfeet]

Hi and welcome.

You will find lots of information and support from all the lovely people of this site.

[Mazcd Partner MPNVoice]

Hello Kevinbros, welcome to our forum, as you can see we are a friendly bunch and very willing to help and advise you as much as we can. I would urge you to read as much as you can on our website mpnvoice.org.uk and look also at the real stories and videos. Best wishes, Maz

[pj1963]

Hello Kevinbros, I was diagnosed with MF in January 2017 and like everyone given this diagnosis was - and still am, to some extent - shocked and rather frightened. This is a wonderful site for sharing information and experiences.

Best wishes to you

Paula