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louslatts

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  • 4 posts
  • Female
  • 01-01-70
  • Living in United Kingdom

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louslatts
Translate   10 years ago

My name is Lou, and for the past 7 years I have had RA Not good as then I was in my 20s I am now 32 well 33 in a few weeks and have only just got on the right tablets for my joints. First off I will tell you a bit about how it affects me some days you feel like all your little joints ie fingers toes knees etc hurt like they are being ripped off. It's worse when you just get up. But it's not just that a lot comes off having RA like the fatigue syndrome with it and the brain fog it makes #life very hard. People might think there is nothing wrong with me when they see me but they don't see me when I am at home and having a bad day. So people always think when you see someone who looks heathy they might not be. Since being on my new tablets it's been ok helped a lot the first lot they gave me made me feel shit. I didn't want to move from my bed. But now I feel I am finally getting somewhere with my treatment. Will try and write a new blog once a day for all. Thank you for reading and take care and good health.

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    louslatts
    Translate   10 years ago

    #life is hard at times. But you have to keep smiling and hold your head up high. The hard times make us happier about the good times in our #life. Money is not everything love and being loved is

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      Translate   10 years ago

      ❤️Love ❤️ Love a word people use daily yet do they mean it. When I say love I mean it. I love my partner off 17 years and I love my mom and I love my cats. I think people need to think before they use this word as if you don't mean it don't say it. These days I think things are being loved and people are being used. Time to get it back to loving people and using things.

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        louslatts
        Translate   10 years ago

        Emphasma And #life Coping With This Illnesse Hello, first off I am the partner care giver of my man who has this horrible disease. I lost my father 3 years ago to this disease to. And then just two years after I find out my man has got it. He is only 40 years old and this illness affects him in every way. He had to give up work and now it's rare we go out. He can't even get dresses in the mornings without it taking it out off his body. He goes moody with me over nothing and to begin with I thought it was because he had enough of me, but it was just because he feels angry that he can not do things that he could be even simple things to you and I like cleaning the house he can't do this no more. This is my first ever blog and I hope it helps someone else out there. It's hard for there loved ones as well off them watching them gasping for air it not nice, I will keep my first blog nice and short. Take care everyone and thanks for reading

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        Marjams/jasmine

        Thank you for sharing
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        louslatts

        @marjams your very welcome
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