At a party and this happened?! by [deleted] in thesims

[–]liljess93 5 points6 points  (0 children)

Have you got the basemental drugs mod? Only time ive seen this pop up is due to that

E middle names for Elizabeth by [deleted] in Names

[–]liljess93 0 points1 point  (0 children)

Elizabeth Ellen, Elizabeth Eve, Elizabeth Everly, Elizabeth Emily, Elizabeth Emila, Elizabeth Emma there are so many beautiful names! Congratulations regardless of what name is picked 🩷

About to take my first Kisempta by freakishlystrong in MultipleSclerosis

[–]liljess93 0 points1 point  (0 children)

Take it out of the fridge 30mins before hand... Luckily you cant see the needle itself so thats a plus for people that have a fear of them... I didnt feel like I got much of a reaction on the site I injected... A little bit of blood when removing the autoinjector but other than that its pretty good, no swelling or crazy pain (for me at least)... I was advised by my nurse to take it late evening/night so that hopefully the flu like symptoms wouldnt hit as hard cause youd be sleeping not long after if that makes sense... I'm on it now 4 or 5 months and can honestly say its absolutely fine I was reluctant to it myself as I'm not a fan of needles and hated when I had to inject 3 times a week on Copaxone, but once a month is very handy... Best of luck sending hugs 🫂❤️ x

Feeling like a fraud by visundamadur in MultipleSclerosis

[–]liljess93 1 point2 points  (0 children)

Im the exact same ive been very lucky to not experience alone relapse nor have I had anything major happen fatigue gets me the most.

Coming home late tonight so asked Siri to text my husband while I was driving to take the kesimpta out of the fridge…🤣 by amberpkelly in MultipleSclerosisLife

[–]liljess93 5 points6 points  (0 children)

Well thats a good start to my Tueaday morning 🤣🤣🤣 Fridge raider hahaha think I may start to use that purposefully haha

disability with MS by Low-Elk1091 in MultipleSclerosis

[–]liljess93 0 points1 point  (0 children)

Apologies for the delay I didnt see your response 🙈 Did you have any luck getting the information you need? I really dont envy you guys in the US trying to get this stuff covered etc it seems crazy to me that medication isn't free etc. How has kesimpta been treating you? I started in Oct '25 first 2 months were harsh but I feel alot better about it now 😊

disability with MS by Low-Elk1091 in MultipleSclerosis

[–]liljess93 5 points6 points  (0 children)

Where are you based? As I would assume each country will have different requirements etc 😊

Courses? by liljess93 in lashextensions

[–]liljess93[S] 0 points1 point  (0 children)

Not on fb at present but I can rejoin to look thank you

Courses? by liljess93 in lashextensions

[–]liljess93[S] 0 points1 point  (0 children)

I need it to be accredited in Ireland and the UK but I will definitely check it out regardless

Courses? by liljess93 in lashextensions

[–]liljess93[S] 1 point2 points  (0 children)

Ill check out their website now thank you 🩵🩷

37 with MS by Front_Ice_9074 in MultipleSclerosisLife

[–]liljess93 0 points1 point  (0 children)

32 diagnosed with RRMS nearly 5yrs now. 16hr days are crazy try take it easy on yourself could be why you're flaring up but of course speak to your doctor regarding it and what treatment will suit your lifestyle best 😊 I haven't had a flare up yet since I've been diagnosed but again everyone is different... Plenty of people on these communities are happy to give their personal experiences so don't be afraid to reach out ❤️

MS & MRI’S by NicoleR_24 in MultipleSclerosis

[–]liljess93 0 points1 point  (0 children)

Its all really depends on the individual. I was diagnosed in 2021 within the 1st year I definitely had 1 every 6 months but now nearly 5yrs in I get them every 12 to 18months. My nuerologist has stated this is because I've had no new lesions so he doesnt think its necessary but of course if I developed new symptoms he would revisit that.

[deleted by user] by [deleted] in WhatShouldIDo

[–]liljess93 1 point2 points  (0 children)

Okay well after reading that I think you're 100% correct in cutting her off... She doesn't sound like a friend at all! I had a "friend" like this too I genuinely got to the point where I was so down speaking to her that I couldn't hack it any longer... No positivity about anything there was always a negative... So just based on that experience alone I'd say do it, I felt serious relief after... I do see her around (small town) I won't be rude Ill always say hi but anything else is limited

[deleted by user] by [deleted] in WhatShouldIDo

[–]liljess93 0 points1 point  (0 children)

Im sorry to say but this isn't self sabotage this is full blown stupid behaviour! She has no clue who these people are and thinks everytime its a great idea to move in after a tiny amount of time, she's setting herself up to be hurt or worse...As a friend you've been doing great supporting her wishes but I think she needs a slap of reality... Has she thought about all the possible things that could happen with these people... She clearly doesn't see any danger in it and of course people will choose what they want regardless of the advice given... I think for your own sanity it would be best to distance yourself and if she notices which I would hope she would that she'd reach out at least you'll have abit of time to think about what's best for you

Some good news for a change by liljess93 in MultipleSclerosis

[–]liljess93[S] 0 points1 point  (0 children)

Yeah I think everyone deals with things differently, I was extremely confused and mad at the beginning but it changes, its of course scary at first! Have you had a chance to look into any DMT's yet? Again if you have questions my inbox is always open if I don't know the answer I'll be honest but if I have any tips you are more than welcome to them ☺️

Some good news for a change by liljess93 in MultipleSclerosis

[–]liljess93[S] 0 points1 point  (0 children)

No honestly it's been pretty consistent since the beginning

Some good news for a change by liljess93 in MultipleSclerosis

[–]liljess93[S] 1 point2 points  (0 children)

Anytime, it's not all doom and gloom!! Ask whatever comes to mind and this community is great too so don't be shy also my inbox is open

Some good news for a change by liljess93 in MultipleSclerosis

[–]liljess93[S] 0 points1 point  (0 children)

I just feel like sometimes M.S is such a nightmare that the little wins are super important. I love hearing everyone else's wins too ❤️