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Mindy

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Hi there Mindy, and welcome to the group! Quick intro so we're not

strangers & #61514; I'm 26 years old, married, diagnosed with RA early last

year. I am on Prednisone, it's the only thing I can take as I'm trying to

have a baby - I know the side effects are not good but it's worked wonders!

I've been really bad on keeping up on the posts but have been trying to

catch up after a break and never seem to manage! Just wanted to tell you

that it's normal to be scared when you first hear that you might have RA, I

felt the same way. I was diagnosed about 8 months ago and was totally

crippled with the pain till they found out what was wrong with me. It's kind

of like a grieving process in the beginning (I know the word might seem

misplaced but I really felt that way - grieving for something lost - and you

go through the same process, Shock, crying your eyes out, anger and then

acceptance.) I was terrified of not being able to keep up with my husband

who's only 27, and we had a very active lifestyle. Now I have a wonderful

doctor and Rheumatologist and with the right medication am managing to carry

on my life almost as well as before. I have a new very demanding job that I

was terrified to accept as I was offered it just after my diagnosis, but I

decided to give it a try and just see what happens. I've been there for 4

months now and even though it's hard with the fatigue sometimes I am so

happy that I did take the opportunity because things are turning out to be

much better than I expected. In the beginning you think this is it - the

end of my " normal " life but after imagining the worst I realised that if you

get the right treatment and a bit of luck you really can live a normal life

with this disease. Try to take one day at a time. I hope that you can find

some support here. By the way I read your cracking knuckles question - not

silly at all : ) - I know what you mean, I get the exact same feeling and

for a lot of joints besides the knuckles.

Hugs,

Heidi

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Hi Mindy...have you been screened for fibromyalgia? Many of us with

fibro experience lots of forgetfulness we call " fibro fog. "

Keep being your own best advocate, and keep coming here for

understanding, support & encouragment.

Hugs of Hope...

Tess

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