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Hi Everyone Options
Rose-B
#21 Posted : Thursday, May 12, 2011 10:28:48 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 4/20/2010
Posts: 1,749
Location: Somerset


Good news long may in continue


x
crazychick
#22 Posted : Thursday, May 12, 2011 1:36:26 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 12/6/2009
Posts: 177
Hi Patti

Just wanted to say hi to you. I'm Shirley, married with 3 children and 3 grandchildren. I was diagnosed just over 2 years ago, aged 47.

I no longer work as my part time work was too physical and i still find the tiredness difficult to cope with.

I've been on 5 DMARD's and failed on 4 so now on MTX and Humira although i have had to miss the humira for a few weeks as i have vasculitis and also had an infection.

It will be nice to get to know you.

Love Shirley x
sheila_G
#23 Posted : Thursday, May 12, 2011 2:07:38 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 3/28/2011
Posts: 956
Location: North Preston
Hi Pet. I don't understand why you have to wait so long for your appointment to start mxt. As far as I know you can go to whichever hospital you choose. If you can drive and have access to other hospitals I would check them out (rheumatology wisSheila x
Kathleen_C
#24 Posted : Thursday, May 12, 2011 4:07:31 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 12/3/2009
Posts: 1,689
Location: Durham
Hi Pet,

You can change hospitals to any one that you feel would suit you better. I changed from a hospital in Durham to one in Newcastle. My GP was happy to write a referral, and I didn`t wait very long for an appointment.

Kathleen C x

LynW
#25 Posted : Saturday, May 14, 2011 1:21:49 AM Quote
Rank: Advanced Member

Groups: Registered

Joined: 12/4/2009
Posts: 2,127
Location: Thornton Cleveleys
Hi Petti

Sorry to be so late with my welcome (if you have a look at this thread you will understand why ... but be prepared for a good laugh!).

Welcome to the forum. A great place to be for support and information; lots of folk, lots of knowledge and a wealth of tried and tested experiences! Glad you have found us and NRAS!

I'm Lyn, married to Mike, we have four children (well I call them children but perhaps it's time to stop!), Abby 23, Ian and Jake 17, and Louis 16. All four in various stages of education! We live in Thornton Cleveleys in north west Lancashire. I was diagnosed with RA 23 years ago and have since run the gamut of medication and had lots of surgical procedures along the way. Currently on Enbrel, Leflunomide, Prednisolone and Naproxen, and a wagon load of pain killers! Struggling at the moment after knee surgery last summer, a major flare in Cyprus of all places, two lots of knee aspirations and joint injections in 7 weeks, a depo injection that didn't work and basically RA that has not been controlled for the last 12 months! But heyho... no-one said life with RA would be easy and all the lovely friends I have made make it very worthwhile (mostly!)

I do hope you are started on medication very soon. The guidelines are the earlier the better. If you're not happy do consider changing hospitals at this stage because you're going to be seeing plenty of them in the future.

Good luck with whatever you decide. Do keep posting, look forward to getting to know you Smile

Lyn x
My son, Ian, completed the BUPA Great North Run on 15th September running for the National Rheumatoid Arthritis Society (NRAS). You can read his story at http://www.justgiving.com/ianlukewilson

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