Hi Everyone!
Well the last few days have been in lupus fatigue. I could barely get out of bed. However, I had to go to the dentist for a teeth cleaning, and do some grocery shopping. Thank the gods Mr. M. goes
with me.
This image is so true.
I know what I want to say but just can't find the words. Or I will be in the middle of a sentence and I can't think of the next word. The brain fog upsets me most of all, especially in public. People can be pretty mean. At home Mr. M. and I laugh about it. Hey, if I don't laugh I will cry and I don't want to do that. I don't want to feel bad or sorry for myself and I don't want anyone else to either.
Have a good evening!
Nicole
P.S. Yeah I know whoever made this meme didn't spell purse correctly. 😁
P.S. Yeah I know whoever made this meme didn't spell purse correctly. 😁
19 comments:
Thyroid fatigue was bad, but at least there's a pill that helps. This sounds like a tough thing to deal with. Of course, there's so many tough things to deal with with lupus, isn't there? Hope you are having a feeling better week Nicole. hugs-Erika
Good advice there Nicole, so many people come with advice and really wouldn't have a clue for they are not in your shoes. Take care.
I recently had a day when I had to drag myself around, so I can imagine how terribly difficult it must be to have many days like this where rest doesn’t even restore you.
...make each and every day the best possible.
That kind of prolonged, bone deep weariness sounds very distressing. Plus brain fog? Not fun.
It sounds similar to ME. Some days are worse than others and there's no predictability.
Nicole I'm sorry this is part of your life. But your strength is contagious, and I need that right now for some things I'm facing. When I can, I'll blog about it. Thanks for being strong. Love ya...
Hopefully you feel better soon and feel less tired! :-D
Feel better soon-Christine cmlk79.blogspot.com
Nicole, bless your heart. I am so sorry that you are living with this. Thank you for sharing about this.
Fatigue is the worst, isn't it? Life doesn't stop but the energy does. I know you are treating yourself gently -- at least I hope so.
Boa tarde minha querida amiga Nicole. Através do seu Blogger, conheci um pouquinho sobre o lúpus. Sei que é uma doença muito séria. Uma excelente tarde de quinta-feira e um grande abraço do seu amigo carioca, que amanhã fará aniversário.
Sending good wishes and hoping you feel better soon.
All the best Jan
I am glad you have the support of your spouse.
Dear Nicole, lupus really does throw a lot of obstacles in the way of those affected. I'm glad you're a warrior, but I can also understand that constantly fighting is exhausting...
Hugs and all the best from Austria, Traude
I can relate and know exactly what you are going through. Glad you have a support system (husband) at least. There are days I wish I had someone to rely on when my lupus flares up.
Olá, não desejo isto a ninguém, compreendo-te, eu tenho Fibromialgia, dores por todo o corpo, não é agradável, não é.
Desejo-te um dia calmo e ensolarado.
Abraço!!!
Thankfully, no one in my circle has this dreadful condition, but I have been pleased to become more informed about it. It really is awful.
Sorry to hear that you're going through a really rough time, hope you are feeling better soon.
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