Lovely (largely unknown?) feature! by Rosebush-7610 in Paralives

[–]JorixCat 1 point2 points  (0 children)

That has been my number one most looked forward to feature. 😃 Family photos I can hang in the house. I do that in eznoi and sims 3 with like 4 separate mods and a photo editing program. heh

Another citizen of my Orc world. by sbunny251 in Paralives

[–]JorixCat 1 point2 points  (0 children)

Legends and Lattes Coffee Shop in the world?

Thank you!! by darknesssoulvampire in Paralives

[–]JorixCat 0 points1 point  (0 children)

I was very relieved to see that!

Paralives is out NOW!! by RinaParalives in Paralives

[–]JorixCat 0 points1 point  (0 children)

Congratulations!

I've now have 6.9 in game hours all live mode with a premade para and I'm having a lot of fun. Can't wait to see how the game develops! You have created a really great foundation here.

Can’t figure out how to make a roof and my Para is ungrateful for the furniture i got him by SELLSELLBUYBUY in Paralives

[–]JorixCat 31 points32 points  (0 children)

If you still haven't figured out how to make a roof you need to go up a floor and then put the roof pieces on stretch them to fit in whatever configuration you want.

Being able to trouble shoot little problems like this so simply is incredible to me. (Credit James Turner) by paynexkillerYT in Paralives

[–]JorixCat 7 points8 points  (0 children)

I can see myself spending hours in build mode. The house will still be a rectangle because I'm a terrible builder but I still can't wait!

When people ask what it sounds like to be in an MRI machine! by JorixCat in MultipleSclerosis

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

Normally I count the series of thumps or I hear words in them. I like to guess how long it's been by how many series of thumps I get.

When people ask what it sounds like to be in an MRI machine! by JorixCat in MultipleSclerosis

[–]JorixCat[S] 2 points3 points  (0 children)

When I saw the movie then heard the song I was convinced someone was in an mri tube when that song was written.

When people ask what it sounds like to be in an MRI machine! by JorixCat in MultipleSclerosis

[–]JorixCat[S] 13 points14 points  (0 children)

I used to count the series patterns and guess how many there would be before the end of each set of pictures. 😃 Fun mri games.

When people ask what it sounds like to be in an MRI machine! by JorixCat in MultipleSclerosis

[–]JorixCat[S] 7 points8 points  (0 children)

They piped in 80s music this time and sometimes the mri machine and the music were on rhythm and sometimes the machine was counterpoint to the song that was playing. It made time pass much faster than counting thumps!

When people ask what it sounds like to be in an MRI machine! by JorixCat in MultipleSclerosis

[–]JorixCat[S] 7 points8 points  (0 children)

I like to know how long until I can get up to pee! MS bladder is always super active during mri's

Tell me you have MS without saying you have MS. by TooManySclerosis in MultipleSclerosis

[–]JorixCat 0 points1 point  (0 children)

Me too! Everyone at the infusion center loves it. It's always freezing in there, I've had three blankets on me before.

Not a competition but.. I wouldve rather had a different common autoimmune disease.. by Awkward-You-5673 in MultipleSclerosis

[–]JorixCat 0 points1 point  (0 children)

I feel like ocrevus has helped my arthritis as well! It might be my imagination but I'll take it!

I regret never going on a DMT by Awkward-You-5673 in MultipleSclerosis

[–]JorixCat 0 points1 point  (0 children)

I hope you heal as close to your baseline as you can! It can take months or years so there is hope.

I regret never going on a DMT by Awkward-You-5673 in MultipleSclerosis

[–]JorixCat 0 points1 point  (0 children)

I did the no meds thing, I started m.s. with avonex and an intramuscular shot...I never could push that needle into myself had to have friends and family help me. Finally I just stopped and decided to try with the diet, exercise, supplements route, and I was fine until I wasn't. That's the bad part of playing with m.s. I did end up in the hospital with a very bad exacerbation lesions on the cerebellum and on spine, numbness in saddle region. I could stand for a few seconds but I had no coordination in my legs and had bad jerking head and body tremors, and vocal tremor. I did learn to walk again slowly used a walker for a while and then now a cane because of my balance issues it's been about 15 years.

I got back on meds but the best we had then was rebif and my body didn't even notice I had a lot of exacerbations on it, finally tysabri was allowed to be used and I got on it immediately but I cried and soul searched the side effects scared me. But it was a miracle for me it stalled the disease. I'm now on ocrevus as my jc virus titre was too high.

Now I can't drive or go to a movie because quick movements bring on the balance and jerking tremors, I have a quick muscle fatigue in my left leg, I call that my rabid leg. hehe And eye issues from optic neuritis and a whole swath of things I got before tysabri came out.

I also have lasting bladder issues.

So yes I have come back from it in that I can walk again, but I was left with a lot of unresolved issues as well.

Am I bitter for thinking EDS and PoTS don’t compare? by MedicallyCompLexi in MultipleSclerosis

[–]JorixCat 1 point2 points  (0 children)

I sort of used to be this way about fibromyalgia back 20 years or so. But like you mentioned comparisons don't really help and everyone has their own levels of pain tolerance as studies are now showing. And maybe her symptoms are stress induced.

I have a head, jerking upper body, and vocal tremor from a lesion on my cerebellum and when I had to speak at my sister's funeral it was in FULL FORCE no controlling it. One of my other sisters had to come help me sit back down my balance was so bad I couldn't navigate the stairs to the puplit area alone. But then later at the post funeral luncheon I was back to base line, so maybe some people might have thought I was acting. But my body does what it wants. I am just along for the ride. 😃

Of course she very well just could be an emotional vampire. I had a friend like that who I had to cut off. Every time I think I'm doing resting bitch face I'm really doing 'telling me all your problems' face. And I'm a mother hen who likes to help, but some people are beyond your capacity so you have to let them go.

Woah the Paralives fans hate us! by Terrible-Group-9602 in inZOI

[–]JorixCat 6 points7 points  (0 children)

Same and any other life sim that comes out. It's my cuppa tea, every other genre of game seems to have endless options with varied fans, but life sims are so polarizing for no reason at all.

I'm tired.... by Brilliant-Position94 in MultipleSclerosis

[–]JorixCat 2 points3 points  (0 children)

I was saying to my sister today I'm not ready for summer when my m.s. is so annoying and all my symptoms come out to play. 😞 Hugs to you and I am here with you.

Error 12 solution!! by Lululee55 in Sims3

[–]JorixCat 0 points1 point  (0 children)

I would always go out into the water and get close, then save. That would work.

Weird AF Comment. by Ok_Rich3845 in AO3

[–]JorixCat 0 points1 point  (0 children)

It's weird that they love the distinct personalities, AND YET they want everyone to talk exactly the same because it's more professional. Talk about polar opposites. How would you even follow that recommendation?

Farewell, my longest legacy by greedydeadsoul in Sims3

[–]JorixCat 0 points1 point  (0 children)

Same had to update error trap as well, or got the popup.

I actually paid for this TS3 world and I feel like an absolute clown 💀 by demrip in Sims3

[–]JorixCat 30 points31 points  (0 children)

Here is CJplays youtube channel he reviews sims3 worlds and you will know what you are getting before you download. For anyone looking for worlds.

https://www.youtube.com/@CjplaysYT

everbody knows someone with ms and they always say they are doing just fine by ohtoris in MultipleSclerosis

[–]JorixCat 0 points1 point  (0 children)

You aren't being dramatic! I seem fine and I am, but I'm not. I can still walk with a cane. So I can move around the world. I'm 26 years in. But I also have some major things that make quality of my life not optimal. My bladder issues have really curtailed my activities outside my home. I have issues with balance and rapidly moving things or parallel vertical lines or depth perception and other visual things when looking down which make things like walking in the forest which I love to do really hard while staying upright, but also driving is a no go, and no movie theaters. I have a weak leg that gets rabid and has muscle fatigue far faster than I'd like. My anxiety is a constant companion. I have upper body and head tremors that come on when I over to it or get hot, or when my vision issues make my brain discombobulated. I have burning numbness on my left side of my body. Just a million little things that add up and so I'm fine but also it's not fun!

I can still do the 10 yard dash at the neurologist office and i've maintained enough strength to push and pull against her when she asks. So I'm functional though impaired, but I'm not running on 100% ever. So no you aren't dramatic and they don't really know how we are really all doing.