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#Lifewithms Reel by @chronicfitjourney (verified account) - Looking back, I can see it now.
The signs were there long before my diagnosis  I just didn't know what they meant.

Here are a few things I brushed of
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CH
@chronicfitjourney
Looking back, I can see it now. The signs were there long before my diagnosis I just didn’t know what they meant. Here are a few things I brushed off: 1️⃣ Fatigue that felt like cement in my bones. 2️⃣ Numbness and tingling that came and went. 3️⃣ Vision changes I blamed on “tired eyes.” 4️⃣ Random dizziness that made me feel “off.” 5️⃣ The quiet thought that something deeper was wrong. I share this because so many of us minimize our symptoms until our bodies scream loud enough that we finally have to listen. If you’re in that space right now… please don’t ignore what your body’s trying to tell you. 🖤 #LifeWithMS #MSAwareness #ChronicIllnessCommunity #MultipleSclerosis #InvisibleIllness #AutoimmuneStrong #WomenWithMS #ChronicFatigue #HealingJourney #ChronicFitJourney
#Lifewithms Reel by @mssociety (verified account) - We've seen transformative progress in the care and treatment of MS, leading to advancements that make day-to-day life more manageable for the over 1 m
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MS
@mssociety
We’ve seen transformative progress in the care and treatment of MS, leading to advancements that make day-to-day life more manageable for the over 1 million people in the US living with it. But the truth remains: MS still has no cure and still takes up way too much space in people’s lives, often in ways you can’t see. Symptoms like fatigue, pain, cognitive changes and depression are invisible, but they shape every decision of daily life for people with MS. Even when its effects are invisible, MS is still there. This #MSAwarenessWeek, see MS for what it is.
#Lifewithms Reel by @drtoddmaderis (verified account) - A new study is revealing just how significantly hypermobility affects quality of life, particularly in women with Ehlers-Danlos syndrome.⁠
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The findi
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DR
@drtoddmaderis
A new study is revealing just how significantly hypermobility affects quality of life, particularly in women with Ehlers-Danlos syndrome.⁠ ⁠ The findings are striking. 99% of the women in the study experienced pain. Autonomic dysfunction was worse than in patients with MS, lupus, and rheumatoid arthritis. Depression, fatigue, and migraines were common. And associated conditions like MCAS, POTS, and dysautonomia often go undiagnosed.⁠ ⁠ This matches what I see in clinical practice. Hypermobile patients frequently present with overlapping symptoms that get attributed to anxiety or dismissed entirely. Without recognizing the connection between hypermobility and autonomic dysfunction, patients are left without a clear treatment direction.⁠ ⁠ Flexibility is not the issue. The systemic effects are.⁠ ⁠ Comment POTS and I will send you the study.⁠ ⁠ Follow @drtoddmaderis for more insights on hypermobility and complex chronic illness.
#Lifewithms Reel by @hellocanadamag (verified account) - Christina Applegate couldn't hold back the tears when she learned her memoir 'You with the Sad Eyes' debuted at No. 1 on the New York Times bestseller
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@hellocanadamag
Christina Applegate couldn’t hold back the tears when she learned her memoir ‘You with the Sad Eyes’ debuted at No. 1 on the New York Times bestseller list 🥹📚 The actress, 54, who was diagnosed with MS in 2021, shares raw and deeply personal reflections on her life, career and health journey in the book - and fans clearly connected. “You all made this wildest of dreams come true,” she wrote while thanking readers for their support ❤️ #ms 📽️: #christinaapplegate
#Lifewithms Reel by @msassociation (verified account) - Neurologist and MSAA board member Dr. Barry Singer explains some of the possible signs and symptoms of Multiple Sclerosis

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#LifewithMS #MSawareness
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MS
@msassociation
Neurologist and MSAA board member Dr. Barry Singer explains some of the possible signs and symptoms of Multiple Sclerosis . #LifewithMS #MSawareness #msawarenessmonth #thisisms #multiplesclerosis
#Lifewithms Reel by @multiplesclerosage - Say something❤️
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📸 Source: @ starzz_galaxy on TikTok
All credit are reserved for their respective Owners
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⚠️Credit or delete=> Message @ fixposts
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MU
@multiplesclerosage
Say something❤️ - 📸 Source: @ starzz_galaxy on TikTok All credit are reserved for their respective Owners - ⚠️Credit or delete=> Message @ fixposts - - - - #msfamily#mslife#multiplesclerosisfighter#mswarriors#livingwithms#beatms#lifewithms#mssupport#msproblems#multiplesclerosissucks#msfighters#lifewithanxiety#mscommunity#mssymptoms#multiplesclerosisproblems#pelvictilt#multiplesclerosissociety#mstrust#msuk
#Lifewithms Reel by @multiplesclerosishero - Did you guess the correct diagnosis on our last post🤪 #
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📸 Source: @ simplenursing on TikTok
All credit are reserved for their respective Owners
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MU
@multiplesclerosishero
Did you guess the correct diagnosis on our last post🤪 # - 📸 Source: @ simplenursing on TikTok All credit are reserved for their respective Owners - ⚠️Credit or delete=> Message @ fixposts - - - - #multiplesclerosis#tipoftheday#mswarrior#msawareness#inthistogether#msfighter#mssucks#curems#neuroplasticity#fuckms#mssociety#multiplesclerosisawareness#msstrong#strongerthanms#lifewithms#mssupport#msproblems#multiplesclerosissucks#msfighters#lifewithanxiety#mscommunity#mssymptoms#multiplesclerosisproblems#pelvictilt#multiplesclerosissociety#mstrust
#Lifewithms Reel by @ontheredcarpet (verified account) - Don't miss Jamie-Lynn Sigler in a new episode of "Grey's Anatomy."

In a role that written for her, she plays Doctor Laura Kaplan, a urologist with Mu
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ON
@ontheredcarpet
Don't miss Jamie-Lynn Sigler in a new episode of "Grey's Anatomy." In a role that written for her, she plays Doctor Laura Kaplan, a urologist with Multiple Sclerosis. In real life, Sigler has battled MS for 25 years. Watch the episode January 15 at 10/9c on ABC and streaming next day on Hulu.
#Lifewithms Reel by @ottobock (verified account) - Our neurotech solutions support users coping life with MS. Would you like to test them?

#LifeWithMS #Exopulse #Ottobock #WeEmpowerPeople
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OT
@ottobock
Our neurotech solutions support users coping life with MS. Would you like to test them? #LifeWithMS #Exopulse #Ottobock #WeEmpowerPeople
#Lifewithms Reel by @mstogetherofficial - Molly's marathon journey continues… 🏃‍♀️

You might remember @molly.hugs12 from our Team MS Together London Marathon lineup… and now she's sharing a
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MS
@mstogetherofficial
Molly’s marathon journey continues… 🏃‍♀️ You might remember @molly.hugs12 from our Team MS Together London Marathon lineup… and now she’s sharing a little update on how her fundraising is going! Let’s help cheer her on in the comments by dropping a 👏 #MSAwareness #MSSupport #MSCommunity #MSLife #LifeWithMS
#Lifewithms Reel by @mathew.embry (verified account) - How do you travel with multiple sclerosis?

In this Live Q&A clip, I share how I prepare food, choose hotels, and stay consistent on the road.

For mo
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MA
@mathew.embry
How do you travel with multiple sclerosis? In this Live Q&A clip, I share how I prepare food, choose hotels, and stay consistent on the road. For more information and free science-based resources about multiple sclerosis, visit MSHope.com. #multiplesclerosis #mshope #livingwithms #LifeWithMS #nocheatdays
#Lifewithms Reel by @roche (verified account) - Resilience and partnership: living with MS. 

Today, we meet Thomas, whose life changed in an instant. Flu-like symptoms led to severe vision loss - a
1.7M
RO
@roche
Resilience and partnership: living with MS. Today, we meet Thomas, whose life changed in an instant. Flu-like symptoms led to severe vision loss — and a diagnosis of multiple sclerosis (MS). A flare-up left him in a wheelchair, but Thomas refused to let MS define him. With the encouragement of his neurologist and physiotherapist, he returned to work and founded an MS contact group in Wolfenbüttel, helping others access the support and information he once struggled to find. Resources like the ‘trotz MS’ campaign and a vibrant German patient community gave Thomas the knowledge and confidence to make informed decisions alongside his doctor — and to empower others living with MS. Click the link in the bio to learn more from our Annual Review! 👇

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