Dee Egan
3.1K posts

Dee Egan
@GMsIrishLass
GM's loyal fan since '81• @GeorgeMichael • Cockapoo Mom • Dublin • Views my own • @Rahenyscouts Leader • RRMS Warrior Apr 2020 Ocrelizumab is my Magic Juice
Dublin City, Ireland Katılım Kasım 2011
304 Takip Edilen209 Takipçiler

Celebrating National HSCP day at Clontarf hospital with all our colleagues. Team work makes the dream work. #HSCPDay2025 @CORUIreland
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Dee Egan retweetledi

Beck: Aging & MS. Peak age for smoldering MS lesions? Age 60. New lesions are more likely to become chronic active (paramagnetic rim) lesions with increasing age. New lesions are less likely to remyelinate with increasing age. #ACTRIMS

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@Brandon_Beaber 👏 that’s great news
I was diagnosed during Covid. First symptoms Mar’20, Hospitalised and DX 2/4/20, 1st DMT June’20 #thankful #thisisms
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Diagnosis of MS in Finland is getting faster and faster. A recent study found time from symptom onset to diagnosis was only 4.6 months on average (compared to 10.1 months in 2013), and medication is typically started around 2 months after diagnosis. multiplesclerosisnewstoday.com/news-posts/202…
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@MustStopMS A4 - I was alone in a hospital bed during Covid (Apr 2020) after a huge (first) relapse. I pulled the curtain around my bed after and had a little cry. Then I said to myself “I’m gonna kick MS’s ass 💪🏼” 🤩 #chatms
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Q4 – Were you alone when you got your #chronicillness diagnosis? If not, who else was with you? What were their reactions? #ChatMS
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@MSenIt4life @MustStopMS Hi Patty & sorry only seeing your comment to me just now 😳
I don’t think so but I’ll be more watchful going forward. Thank you for pointing it out 👏 Have a great day 🤗
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@GMsIrishLass @MustStopMS Do you have Focal Aware Seizures?? Your description kinda sounds like it. The ‘floating’, there but yet not.. Do your eyes seem to stare or do you have any type of repetitive movements?? 💜💜
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Q1 – we are approaching the holiday season and many with MS get some sort of “sensory overload” when they have to go somewhere with many people. Do you have any MS related issues with gatherings or get-togethers? What do you experience? #ChatMS
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Q1 – That time when you get officially diagnosed with an illness is filled with many different emotions. Let’s talk about that today. First, when were you diagnosed and at what age? #ChatMS #chronicillness
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@MustStopMS Q3 - just as determined but now armed with lots more good information 👍🏻 #chatms
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Q3 – How do your thoughts today compare to your thoughts at the time of your #chronicillness diagnosis? #ChatMS
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Q2 – When you first got the official diagnosis of your #chronicillness, what was the first thought(s) that entered your mind? #ChatMS
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Dee Egan retweetledi

@MustStopMS @shiftms I love looking OUT at snow ❄️☃️
Also like you, way better in colder temps ✅
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@shiftms Snow. Nah. But I feel worse in colder temps rather than heat like others with MS.
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Does snow (cold weather) affect your MS symptoms?
Shift.ms@shiftms
Last few days the UK (mainly the media) has been in a mild panic of the possibilities of snow My mum woke up to snow she lives in NE England & i woke up to nothing, I live in London 200 miles south My prediction is most will melt in a day or 2 What weather have you woken up to?
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@MustStopMS Absolutely 🤪 I have a few excuses ready and use different ones - if I have to. Thankfully I’m learning which events to accept and which ones to politely refuse. We are learning all the time with MS #chatms
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@GMsIrishLass Does your “get out clause” change depending on the event? #ChatMS
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Q4- What is on your “must do” or “must have” list when attending gatherings or get-togethers? #ChatMS
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@MustStopMS Q5 - if it’s in a noisy pub I won’t go (as I’ve learned the hard way it only aggravates my sensory overload) #chatms
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Q5 – Have you ever opted not to attend a get-together or gathering because of MS symptoms? Even if it was with family?Please explain. #ChatMS
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@mama_withms I must be the “AntiDepression”. DX almost 5 years and I try to be as positive as I always was. Horrible statistic all the same 😳 #chatms #lifewithms
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