Cian Twomey is a video creator from Cork and creates comedic sketches based around his girlfriend/muse Emily Rochford since 2015.
Wow are they still a thing!? I remember videos of him pretending to be Emily circulating Facebook in like 2015 had no idea they were still trying to be relevant.
Yeah he kinda went down hill a little re the comedy when she came on the scene, such a shame I liked him in the early days.Cannot STAND them. I could never understand the appeal? She had a brief stint as a MUA but got addicted to the blow up doll lips and I lost heed after that..
She does seem nice but just donāt understand the make up successI used to follow emily on Instagram. she seems like a really lovely girl in fairness
Well if its ongoing and lasts for long periods of time then it is classified as chronic as its more about length of time than intensity of the disease.Just jumping on hereā¦ I get it that she has arthritis and itās an invisible illness.. I have a few friends who have had it since teenagers. However I donāt believe she has a āchronicā illness as she puts it. If her arthritis was chronic she would hardly be able to move. And I donāt think you can use āinvisibleā and āchronicā in the same context as a physically debilitating disease. She randomly popped up there on my feed and I was like wtf is her page about. Whinging and terrible fashion it seemsā¦.
No youāre way off here! I suffer with an invisible Illness and the amount of people like you who make out it doesnāt exist of affect me because YOU canāt see or feel it isnāt ok. I find this couple really annoying I think I remember them for years ago I canāt believe itās still a thing! But your comment isnāt ok, please educate yourself in this day and age itās 2022. Iām not being rude honestly but I had to fight to be heard because it couldnāt possibly be happening to me at the age I was and it was happening and I was gaslighted by medical professionals til I actually got a formal diagnosis, purely because of my age so donāt do that to herJust jumping on hereā¦ I get it that she has arthritis and itās an invisible illness.. I have a few friends who have had it since teenagers. However I donāt believe she has a āchronicā illness as she puts it. If her arthritis was chronic she would hardly be able to move. And I donāt think you can use āinvisibleā and āchronicā in the same context as a physically debilitating disease. She randomly popped up there on my feed and I was like wtf is her page about. Whinging and terrible fashion it seemsā¦.
This comment is not ok. It is unfair to compare your friends to Emily - Everyone's experience is different. You don't 'believe' she has a chronic illness...?There is nothing to believe - it is a fact.Just jumping on hereā¦ I get it that she has arthritis and itās an invisible illness.. I have a few friends who have had it since teenagers. However I donāt believe she has a āchronicā illness as she puts it. If her arthritis was chronic she would hardly be able to move. And I donāt think you can use āinvisibleā and āchronicā in the same context as a physically debilitating disease. She randomly popped up there on my feed and I was like wtf is her page about. Whinging and terrible fashion it seemsā¦.
Okay didnāt know that. My own friends use steroids to treat theirs maybe theirās are chronic too I never heard to them referred to it as chronic so thatās fair enoughWell if its ongoing and lasts for long periods of time then it is classified as chronic as its more about length of time than intensity of the disease.
I also have a chronic stage 4 illness - endometriosis which took 15 yrs to diagnose. 1 in 7 people have endometriosis. So I understand lots of people have invisible illnesses Iām not bashing that. I was speaking about my own friends who have ARTHRITIS who use steroids to treat it as it can be quite bad and during our discussions they never used the word chronic so I wondered if it applied to this disease also and she continuously goes on about it and physically can walk okay. My friend canāt walk on her bad days but told me before it hadnāt reached chronic stage. That is allNo youāre way off here! I suffer with an invisible Illness and the amount of people like you who make out it doesnāt exist of affect me because YOU canāt see or feel it isnāt ok. I find this couple really annoying I think I remember them for years ago I canāt believe itās still a thing! But your comment isnāt ok, please educate yourself in this day and age itās 2022. Iām not being rude honestly but I had to fight to be heard because it couldnāt possibly be happening to me at the age I was and it was happening and I was gaslighted by medical professionals til I actually got a formal diagnosis, purely because of my age so donāt do that to her
I donāt really think you need to defend yourself to this extent. I didnāt find your original comment that insulting or offensive and Iāve been living with this condition, amongst others, and fighting for a diagnosis (which I eventually got) for years.Okay didnāt know that. My own friends use steroids to treat theirs maybe theirās are chronic too I never heard to them referred to it as chronic so thatās fair enough
I also have a chronic stage 4 illness - endometriosis which took 15 yrs to diagnose. 1 in 7 people have endometriosis. So I understand lots of people have invisible illnesses Iām not bashing that. I was speaking about my own friends who have ARTHRITIS who use steroids to treat it as it can be quite bad and during our discussions they never used the word chronic so I wondered if it applied to this disease also and she continuously goes on about it and physically can walk okay. My friend canāt walk on her bad days but told me before it hadnāt reached chronic stage. That is all
Thank you. I wasnāt to trying to belittle any illness. I also find āeducate yourselfā an incredibly crass response thrown around, I could not imagine saying that to someone who didnāt understand something.I donāt really think you need to defend yourself to this extent. I didnāt find your original comment that insulting or offensive and Iāve been living with this condition, amongst others, and fighting for a diagnosis (which I eventually got) for years.
This is a discussion forum where we are all entitled to our opinions and have the opportunity to discuss them. I donāt think itās fair to just throw the phrase āeducate yourselfā around and I believe it creates animosity whereas discussion and questions are much more healthy. Just my humble opinion.
I followed Emily briefly a long time ago but had to unfollow her as, like you, her page and ācontentā confused me. Iām sure sheās a nice enough person just trying to get by but how she has sustained a significant following after the initial interest surge, baffles me. Her makeup looks are awful, her fashion is terrible and I genuinely canāt understand what people find interesting about her.
I initially found Cianās comedy sketches funny and think he really could have gone places with the right guidance and training. Unfortunately he seemed happier falling into the āinfluencerā category and sold out a bit. Thatās where I think it all went wrong and I believe heās missed his window of opportunity now. Itās a real shame.