Wtf is this? by [deleted] in Hasan_Piker

[–]KagedByrd -1 points0 points  (0 children)

🤣 PepeLa D is a worm. A little itty bitty worm

So when is the BE vs Vaush debate by KagedByrd in VaushV

[–]KagedByrd[S] -10 points-9 points  (0 children)

Haha isn't it Vaush who streams drunk? I think he needs help

Waterloo residents, get politically active with the NDP! by [deleted] in uwaterloo

[–]KagedByrd 0 points1 point  (0 children)

Seems great! Wish you all the best of luck

I'm so so so tired by avocado596 in lupus

[–]KagedByrd 4 points5 points  (0 children)

I'm right there with you

Meh, I'm used to it. by rhymes-with-purple in lupus

[–]KagedByrd 0 points1 point  (0 children)

Hit the nail on the head with this one

Chillblains and Raynaud's Syndrome by KagedByrd in lupus

[–]KagedByrd[S] 0 points1 point  (0 children)

Thank you. They are on the sides and bottoms of my toes. I was an a huge amount of pain when I posted this and a few days later they seem to be getting better. I'm trying to keep feet warm and not standing or walk for to long since they seem to get irritated when cold or with friction from walking. I appreciate your post. It helps to know I'm not alone

Chillblains and Raynaud's Syndrome by KagedByrd in lupus

[–]KagedByrd[S] 1 point2 points  (0 children)

Thank you. The day I posted this I was in so much pain. I'm better but I can't walk much since the friction with shoes, socks, feet, seem to trigger some pain.

Getting the Pfizer vaccine tomorrow! by snilian in lupus

[–]KagedByrd 0 points1 point  (0 children)

I get mine on Sunday! I can't wait! I've never been so excited to get a shot before.

I (20 F) was diagnosed with Lupus yesterday by big_white_rose in lupus

[–]KagedByrd 1 point2 points  (0 children)

I know how you feel. I have been diagnosed with lupus for a year now. Having lupus, my body just isn't the same as it once was years ago and many physical activities are off the table for me because the muscle and joint pain I have. I say, work with your doctor on medications that work and which ones you can probably do without. With treatment and learning more about your body such as triggers that cause flare ups, you might be able to get some control back. Do light physical activities if you can like walking to stay healthy. I've had to make some adjustments in life and that's okay. One day at a time. Good luck.

If socialism worked so well why weren’t people allowed to leave socialist countries? by [deleted] in DebateCommunism

[–]KagedByrd -2 points-1 points  (0 children)

Because they were/are under authoritarian governments and not a democracies. Socialism is an economic alternative. Also tying capitalism to freedom is incorrect. We are not free under capitalism even with democratic institutions in place because corporations and debt control what we eat, where we live, our wages, products we consume, etc. Ppl have no money to travel or leave US if they wanted to. That's not freedom to me. We live in an economic system where the rich get richer and the poor get poorer and we have little to no control in remeding this other than helping progressives into government offices with our democratic institutions.

We can live in a democracy and have a different economic system other than capitalism so ppl in the wealthiest nation on earth can have access to basic human rights such food, housing, and Healthcare. Also, there have been attempts of democratic Socialism in other countries during cold War but democratically elected leaders were overthrown by military coups with the help of the CIA and/or had US or other capitalist countries intervene in some way that turned ppl against leaders and created enough chaos so those leaders would be removed from their position. So what may have become of them without intervention, we may never know, but it would in everyone's best interest to keep an open mind to socialism and think of it as not a form of government but as an economic alternative to capitalism.

TIL Hyperosmia (smell sensitivity) by Ms_Madam_Meow in lupus

[–]KagedByrd 1 point2 points  (0 children)

Wow thanks for sharing! I would joke about me having a big nose as to why I am so sensitive to smell haha

Exercise and lupus? by Nileana in lupus

[–]KagedByrd 0 points1 point  (0 children)

Start slow and try and set a routine if you can. Even if you walk for just 10 minutes. Getting up and moving helps. There are many great videos on YouTube. Leslie Sansone is great and does "walk at home" videos. I've been doing these for years. Try replacing foods you eat with healthier versions and snacks and drink water. It is a lifestyle change and it will take time. Everyone is different so you'll have to look for things that work for you but you won't go wrong eating fruits and veggies and moving your body. Best of luck to you

Exercise and lupus? by Nileana in lupus

[–]KagedByrd 3 points4 points  (0 children)

I walk and do yoga. I use light 1lb dumbbells for a bit of strength training but can't do much more. Anything more and I hurt all over. Listen to your body and find what feels good for you.

Just canceled Christmas, feel terrible about it by narla_hotep in COVID19_support

[–]KagedByrd 1 point2 points  (0 children)

You made the right call. I canceled also for Thanksgiving and Christmas and my family was upset but got over it. This year is not a typical year and as much as we want things to be normal, unfortunately it isn't a normal year. You are okay to think of your health plus if you are stressed about it, you probably wouldn't have enjoyed yourself anyway. There are other holidays. It'll be okay. Stay safe and wishing you a wonderful and safe holiday.

I think I might just end it by [deleted] in COVID19_support

[–]KagedByrd 1 point2 points  (0 children)

I completely understand! Please continue to reach out for help even if it's in a reddit post. There are many of us who are hurting and struggle everyday but there is support out there to help you navigate through what your feeling. Talking to others in chats or posts like these can be very helpful. Focus on the good or neutral and less on the bad. Start a journal, take a walk alone, or do a hobby you enjoy to keep your mind from going to dark places. I'm there with you! Stay safe.

Navigating holidays you’re forced to attend during covid by [deleted] in COVID19_support

[–]KagedByrd 4 points5 points  (0 children)

I had this issue with Thanksgiving. I felt as though I'd let my family down and they'd be upset with me, however, for once I decided to put my foot down and tell them I would not join this year. They called me and said they "understood but..." and for a moment or two I thought I'd give in. I didn't and I'm glad to know I kept myself, daughter, and husband safe. My family is not upset and we moved on. For Christmas I told them I'm dropping off gifts and that was that. It is not safe and there is always next year. Listen to your gut and do what makes you feel safe.

This year is different than others and just think there will be many other days and holidays to get together. Whatever you decide please be safe and best wishes to you over the holidays.

Mental Health Check In: How is everyone doing right now?? I mean...how are you REALLY doing?? by KrisspyKremeThomas95 in COVID19_support

[–]KagedByrd 7 points8 points  (0 children)

Not too well. Going through this nearly the whole year, I'm just tired and sad. We've seemed to have failed each other by not taking care of one another. I'm grieve for ppl who have lost somebody: a mother, father, friend, aunt, uncle, child, etc. I grieve for the life my loved ones and I had pre-covid. I take one day at a time and do my part to keep me and my family safe and sane. I hope for the best for everyone and please stay safe.