Hi haven't posted on this 'new' board...

tiddleyboo

Hi!
I've been a member of these forums for a while but there never used to be a parents of JIA kids bit :-)
I have a 6 year old daughter who has 'extended oligo' aka polyarticular! Shes had it since 2 years (possibly symptoms before) and is on methotrexate. We've just had dosage increase after a flare up-still awaiting mtx to kick in!
I also post on the Facebook group which has been very helpful and supportive.
Is there anyone in the Cambridgeshire area?
Look forward to getting to know you all!

CherryDrops

Hi Tiddleyboo!
I havent been here too long but my 10 (almost 11yr old) daugher has poly art and also a disease called Morquio (MPS4A). She is currently on mtx and prednisolene, only diag in feb this yr but have been suffering with various things for a looonnngg time. We do not live in cambridgeshire unfortunately, we live in lincolnshire but I'm still happy to 'chat' cyber or otherwise! They seem a very friendly bunch on here and there is normally someone who knows/understands what you are going through at different stages etc. I also post on the FB page too - it is def a great source of info!
keep smiling and chat soon.

Pegsboard

Hi. I have a daughter who's got oligo arthritis. She's 3 and due to start MTX soon. What's the face book page? Didn't know there was 1!
I live in Yorkshire but, like cherry drops, am happy to chat when I can on here.
Zoe