Waiting, 21 years later
People with neurological illnesses walk in and out of the waiting room. Quite often, the illness feels bigger than how its carrier believes it ever will be.
Posts by Ireland, Multiple Sclerosis & Me
Trump: "I'm good with languages."
The world: "Sure you do."
Paradoxes
Despite my urgency to find my footing in a world transformed by MS, I found myself in need of time and space to delve deeply within, to re-establish myself amidst an onslaught of new normals. Adapting to something so wildly unpredictable, the relentless cycle of adaptation was not only…
Hey Hegs, you might want to refine the meaning of "The most lethal, most complex aerial operation in history" if all you can do is kill girls in a primary school in #Iran, unless that was the plan altogether.
#Pentagon #PeteHegseth #DeptofWar
So, when will the criminal WH occupier & his enablers be arrested?
www.mediaite.com/media/news/b...
#EpsteinFiles #AndrewArrested
#TrumpEpsteinFiles
MS: Feeling seen doesn’t always mean feeling heard
#EDHbestblogs #MS #MultipleSclerosis #Ireland #MSAwareness #neurology
#MSWarrior #MSLife #InvisibleIllness @EverydayHealth irelandms.com/2026/02/08/m...
I rarely curse but my god, #PamBondi is such an arrogant b*tch. #Epstein victims sitting behind her & she shows not one ounce of empathy. She should be disbarred immediately. #DOJ
MS: Feeling seen doesn’t always mean feeling heard
Despite this, I often refer to MS as a lonely illness. With a vast array of associated neurological and non-neurological symptoms spread over four different types of MS, it will be exponentially difficult to find someone who has the exact same…
To my brother, gone 19 years too many. You’re not in that faraway place I cannot escape to just yet. irelandms.com/2026/01/25/b... via @WillekeVE
#MSinIreland #multiplesclerosis #Family #neurologyIreland #bereavement #grief
To my brother, gone 19 years too many
I still miss your quiet support when you guided me when I needed strength. You were more than a brother; you were my first hero, a steady presence in my life, an unspoken promise that you’d always have my back.
Top 10 MS news stories of 2025
Throughout 2025, the team at Multiple Sclerosis News Today brought readers the latest advances and updates in research related to multiple sclerosis (MS). Here are the top 10 most-read news stories MSNT published this year.
Happy 2026, or how time flies when MS is stealing time
You see, in my head, my resolutions have already borne plenty of success. In reality, crippling fatigue and facial nerve pain have halted even more tasks, projects and mighty dreams, but, LGO*.
[NEW] "When sensory MS symptoms enter your system, you will find yourself worrying if what your feeling is even real. So while you're reading this, I'm whacking the imaginary hair planted by multiple sclerosis off my face again."
#multiplesclerosis #ms #symptoms
irelandms.com/2025/10/24/s...
Sensory MS symptoms: The hair that isn’t there
While you're reading this, I'm writing and whacking the imaginary hair planted by multiple sclerosis off my face again. For the n'th time today. If this goes on for another few hours, I will have to report myself for abuse of hair follicles.
#ZelenskyyUa It pains me to say this: #POTUS #lDonaldTrump only expressed support for #Ukraine to keep a good image with world leaders, not out of real concern for you. He will soon turn negative again as his loyalty still lies more with Putin. Please tay strong #SlavaUkraini
#UNGA
Please mock #POTUS #realDonaldTrump on the #UN stage. His thin skin and enormous ego will crack before your very eyes as his fear of being a #ConvictedFelon US President, combined with the #EpsteinScandalAndCoverUp needs to be highlighted on a global scale
www.cnn.com/2025/09/23/p...
After the Mueller report breakdown debacle, Barr's 2020 condemnation should've been far stronger, knowing what Trump was capable of. Not that it mattered because Barr said he'd vote for Trump in 2024 regardless. Anything he says is just too little, too late.
Look at the 1st image, it is utter devastation and heartache, yet @netanyahu @POTUS seem to enjoy the insanity of their megalomania, fed by @realDonaldTrump's dreams of #Gaza Plaza. They should both be tried in @ICC
www.cnn.com/2025/09/16/m... #GazaGenocide #GazaIsStarving
Claiming that routine immunization requirements for school are an issue of parental rights dehumanizes children. Kids have intrinsic rights just as anyone, and parents are obligated to provide the best care possible for them. That includes providing them with indicated medical interventions.
Halleluja! So many books, so little time.
medium.com/@leighlovesh... #psychology #Intelligence #Insight #AI
#POTUS fled from the #G7Summit because, A) his ego is still badly damaged after the poor attendance of his @USArmy party; B) just like 2018, because he didn't want to be confronted by world leaders about still unnegotiated #tradedeals. Poor baby, right?
www.mediaite.com/politics/the...
🧡 Happy World MS Day! 🧡
"Within your diagnosis lies the potential for transformation. It will forge your strength in profound ways, but you can and will thrive despite #MS." @MSIRELAND #MSIreland #EDHbestblogs @EverydayHealth @teva #LifeEffects @WorldMSDay irelandms.com/2025/05/25/w...
MUST WATCH: ICE kidnapped a disabled American citizen.
Her name is Alma Bowman. Born in the Philippines while her dad served in the U.S. Navy.
She’s lived here 48 years.
They crashed her wheelchair, denied meds, cut her off from her lawyer—and jailed her.
She. Is. A. Citizen.
#WorldMSDay "Despite your #MS #diagnosis, you still thrive. You're still walking, literally, despite nerve pain & excruciating facial nerve pain that is hard to describe and even harder for others to believe." #multiplesclerosis #EDHbestblogs #EverydayHealth #MSIRELAND
irelandms.com/2025/05/25/w...
#WorldMSDay "Despite your #MS #diagnosis, you still thrive. You're still walking, literally, despite daily nerve pain and excruciating facial nerve pain that is hard to describe and even harder for others to believe." #multiplesclerosis #EDHbestblogs #EverydayHealth #MSIRELAND
World MS Day 2025: What I would tell my newly diagnosed self: "You still thrive despite facial nerve pain that is hard to describe-and even harder for others to believe." irelandms.com/2025/05/25/w... #WorldMSDay #MS #diagnosis #MSIRELAND #multiplesclerosis
irelandms.com/2025/05/25/w...
World MS Day 2025: What I would tell my newly diagnosed self
Within your diagnosis lies the potential for transformation; it can either forge our strength or test our resolve, shaping us in profound ways. Mine was no different. Find out what I would tell my newly diagnosed self twenty years ago.