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Graphic announcing new talk show episode titled What I Wish I Would've Known After Diagnosis. Headshots of Leila and Deb below the talk show title.

Graphic announcing new talk show episode titled What I Wish I Would've Known After Diagnosis. Headshots of Leila and Deb below the talk show title.

A new diagnosis can bring relief, fear, and uncertainty all at once. Get advice directly from the AiArthritis community for those newly diagnosed with an AiArthritis disease.

🎙️Listen now: zurl.co/R8BV8

#AiArthritis #HealthPodcast #DiseaseManagement #NewlyDiagnosed #PatientAdvice #PatientEducation

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Signed,

2.9 million people worldwide living with MS

#MultipleSclerosis #TheMighty #caregiving #disability #ChronicIllness #newlydiagnosed #autoimmune

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Newly Diagnosed resources from the MS Society:
When you need it, support is all around you.

Go to nationalmssociety.org/understanding-ms/newly-diagnosed

#MultipleSclerosis #TheMighty #ChronicIllness #caregiving #newlydiagnosed #autoimmune #disability

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Feeling intimidated or lost at the doctor's office? (Me too.) Check out this Thursday's Ask an MS Expert: "How to Talk to your Healthcare Provider," on 2/26/26 at 12-12:30 p.m. ET. (Originally aired 1/11/24.) tinyurl.com/mvayrry9

#MultipleSclerosis #TheMighty #newlydiagnosed #autoimmune #disability

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Got the Diagnosis Blues?

#newlydiagnosed #MultipleSclerosis #ChronicIllness #autoimmune #TheMighty #caregiving #disability

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Caregiver Panel: Bridging the Gap The United Spinal Association Care Support Working Group hosted the Caregiver Panel: Bridging the Gap. This national panel brought together caregivers from across…

From the United Spinal Care Working Group, an excellent monthly club for support, resources and advocacy.

vimeo.com/1158497418?f...

#caregiving #MultipleSclerosis #TheMighty #ChronicIllness #newlydiagnosed #autoimmune #disability
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Pediatric MS Resource Guide — info and support.

Requested by a new member.

nationalmssociety.org/for-professionals/for-healthcare-professionals/managing-and-treating-ms/pediatric-ms

#PediatricMS #POMS #MultipleSclerosis #MightyTogether #ChronicIllness #caregiving #newlydiagnosed #disability

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Were you or your child just diagnosed with a #foodallergy? Did you know as many as 32 million Americans live with #foodallergies?

Visit #FAACT to download our #NewlyDiagnosed Guide:
www.foodallergyawareness.org/food-allergy...

#Allergy #Anaphylaxis #AllergyAwareness #FoodAllergyAwareness

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This Monday, Jan. 12, 7–8:30 p.m. ET.

#MultipleSclerosis #ChronicIllness #caregiving #newlydiagnosed #autoimmune #disability

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Were you or your child just diagnosed with a food allergy? Did you know as many as 32 million Americans live with #foodallergies?

Visit #FAACT to learn more:
www.foodallergyawareness.org/food-allergy...

#FoodAllergy #Allergy #NewlyDiagnosed #Anaphylaxis #FoodAllergyAwareness #AllergyAwareness

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What helped you cope with your #ChronicIllness or MS? What made you Mightier?

#MultipleSclerosis #newlydiagnosed #disability #caregiving #autoimmune

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Vaccinations with MS
Vaccinations with MS YouTube video by National MS Society

With flu hitting hard this winter, how does protecting ourselves w vaccinations affect #MultipleSclerosis & #autoimmune conditions?
In this Ask an MS Expert segment, Dr. Lisa Doggett looks at how shots for flu, COVID, RSV, pneumonia etc. affect people w MS like herself. #Vaccinations #newlydiagnosed

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For all your MS-related questions,

MS Navigators 800-344-4867

email contactusnmss@nmss.org

or live online at www.nationalmssociety.org/resources/get-support/ms-navigator

#MultipleSclerosis #newlydiagnosed #disability #caregiving

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#NewlyDiagnosed
#BipolarAwareness
#MentalHealthMatters
#BipolarSupport
#MentalWellness
#UnderstandingBipolar
#BipolarResources
#MentalHealthSupport
#YouAreNotAlone
#BipolarJourney

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Info on MS & symptoms, how to manage & live well with MS. Ask your questions, share your experiences with others.

Register at engage.nationalmssociety.org/new_to_ms_december_2025_virtual

#MultipleSclerosis #newlydiagnosed #disability #caregiving #autoimmune

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Tonight 7 PM ET, Virtual Caregiver Support Group

3rd Thursday of each month at 7-8 p.m. ET
Contact: Judy, jsfisch@rcn.com

from the #MultipleSclerosis Society
#ChronicIllness #NewlyDiagnosed #Disability

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Home Movieguide® reviews movies from a Christian perspective for families and works in Hollywood to redeem the media.

Source: "Why This County Star Feels ‘Blessed’ as He Battles Multiple Sclerosis" by Gavin Boyle, Movieguide.com.

#PainManagement #Spasticity #Baclofen #newlydiagnosed #disability #caregiving #autoimmune

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First Holiday Season With a Newly Diagnosed Child? Navigating the Gaps and Finding Solutions!

Read #FAACT's full blog here:
www.foodallergyawareness.org/blogs/entry/...

#FoodAllergy #FoodAllergies #Allergy #Anaphylaxis #FoodAllergyAwareness #AllergyAwareness #Holidays #HolidayTips #NewlyDiagnosed

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Continuous glucose monitor graph showing blood sugar spikes after eating.

Continuous glucose monitor graph showing blood sugar spikes after eating.

Recently diagnosed with LADA diabetes. Got my hands on a CGM sensor to see what my pancreas is up to. Needless to say I think I need insulin!
#LADA #LADAdiabetes #T1D #type1diabetes #newlydiagnosed #DOC

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Now let em stare. ;)
#MultipleSclerosis #newlydiagnosed #disability

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National MS Society

Pathways to Wellness With MS: Maternal Health — Thurs. 7/17, 6 PM Eastern

with neurologist Deja Rose, MD of the Cleveland Clinic and Emory University.

Sign up — secure.nationalmssociety.org/site/Calenda...
#MultipleSclerosis #MightyTogether #newlydiagnosed #disability #caregiving #autoimmune

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APS Foundation of America, Inc. | Antiphospholipid Syndrome - APS

Learn More
Visit apsfa.org for trusted information, patient resources, and ways to connect with others who understand.

#WTD25 #raredisease #charity #donate #newdiagnosis #newlydiagnosed #AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch

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Empowering people affected by MS to live their best lives The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS.

There's so much support out there for us to take advantage of.

Here are Newly Diagnosed MS Resources from the MS Society.

#multiplesclerosis #newlydiagnosed #disability #caregiving

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Helpful info, positive message:

Damien Washington has a ton of fun, useful vlogs on MS-related topics we can all relate to. He's someone who feels like a friend.

www.damianwashington.com/vlogs/

#multiplesclerosis #chronicillness #newlydiagnosed #disability #caregiving

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I get by with a little help from my friends.

This program's been going for decades, because it works. You're not alone.

#multiplesclerosis #newlydiagnosed #disability

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Newly Diagnosed With Type 2 Diabetes ... Or Type 3c Diabetes or LADA ... Who Knows! I was surprised by my recent type 2 diabetes diagnosis because I didn't have prediabetes and my A1C shot up quickly.

Newly Diagnosed with Type 2 Diabetes

I was surprised by my recent type 2 diabetes diagnosis because I didn't have prediabetes and my A1C shot up quickly.

open.substack.com/pub/leighann...

#newlydiagnosed #diabetes #type2diabetes #T2DM #LADA #T3cDiabetes #T3cDM #PPDM #PAPD

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Why Friends Abandon You During Illness | Chronic Illness & Friendship Why do friends abandon you when you're sick? Explore the emotional impact of losing friendships during chronic illness and how to cope with abandonment.

Chronic illness made me tough. But there's one friend disappearance that still messes with my head, 20+ years later.

"Why do friends abandon you...? Is it discomfort, avoidance, or something deeper?"

#multiplesclerosis #chronicillness #disability #newlydiagnosed

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MS is a disease of uncertainty — and that all starts during diagnosis.

But diagnosis times are generally decreasing and treatments getting more effective.

#multiplesclerosis #chronicillness #autoimmune #newlydiagnosed #disability #caregiving

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Approximately 50% of MS patients will experience some optic neuritis.

Excellent page on info and symptom management — www.nationalmssociety.org/for-professi...

#MultipleSclerosis #OpticNeuritis #chronicillness #autoimmune #newlydiagnosed #disability #caregiving

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This how it was my $1000/mo MS drug too (which also looked exactly like water, just sayin').

#multiplesclerosis #chronicillness #autoimmune #newlydiagnosed #disability #caregiving

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