Does anyone on this website live in the Bournemouth area?

[netty64]

I was just wondering if anyone on here lives in the Bournemouth area and when we are able to have contact with others, whether anyone would like to meet up and maybe for a reality support group?

[SDJD]

Hi Netty, I live in Wimborne. I was diagnosed with ET in 2017. It would be good to meet when we are allowed. Hope you are keeping well.

Love Suzy x

[netty64 in reply to SDJD]

Hi Suzy, I was diagnosed with ET just before xmas.

Take care and hope see you soon

Annette

[Quercus53]

Hi Netty, I'm in Broadstone!

[hunter5582]

If you click on the "More" button there is a "Find People Near Me" function.

[netty64 in reply to hunter5582]

Thanks

[Corfe3000]

Hi Netty, I also live in Wimborne and have ET x

[netty64 in reply to Corfe3000]

Seems like there are quite a few of us that live in the Bournemouth area, will be great to meet up when able x

[mrbrindle]

Hi Netty,

I’m in Ensbury Park, was diagnosed 5 years ago with PV. Started Hydroxy around 5 months ago, so no more venesections .A few side effects as I have read many of you have.

Yes would be great to meet up

All the best

[Sunny699]

Out of interest, Who are people seeing locally? and do you have any feedback? have you been referred to see a specialist anywhere else?

I have had a first session with the haematology department in Poole, I got the impression from that the lady I spoke to that she may not be that experienced with ET.

[netty64 in reply to Sunny699]

I'm under Haematologist Dr. Allotey at RBH

[mrbrindle]

I’m at RBH under Dr Chacko. He’s very thorough and talked me through everything before commencing with Hydroxy