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Some mornings, my wife wakes up w extended bouts of dizziness. She's also my caregiver, so those days become "bed days" as we focus on her well-being.

Because "MS care" = "family care," and vice versa. This Thurday's "Ask an MS Expert" is about managing MS when both spouse AND carepartner need health supports.

Join Kathleen Silva, who shares her similar experience of caring for her husband, Rick, who lives with MS, while she faces cancer. Learn what it means to manage care together and how additional support can help ensure that everyone involved is supported.

Ask an MS Expert: "Managing MS as a Team." Thur., 7/2/26 @ 12–12:30 p.m. ET. tinyurl.com/3cmb9bwp

#MultipleSclerosis #MightyTogether #Caregiving #ChronicIllness #newlydiagnosed #autoimmune #Disability

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.
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I'm new here!

Hi, my name is CancerRamblings444. I'm here because I want to share my story, my experience and my book Cancer Ramblings with this community.

#MightyTogether #Cancer

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I lost my daughter Lily yesterday. I don’t know how to survive this.

I am heartbroken to share that my daughter Lily passed away yesterday after our time in the ICU.

Losing her after already losing my wife to cancer is a profound tragedy, and it has been a traumatizing time for both me and her younger brother. I am finding it incredibly difficult to navigate this immense grief and handle the day-to-day reality right now.

Because I am struggling to find the words or communicate clearly in my current state, I am reaching out to this community for comfort, guidance, and support.#Depression #SystemicLupus

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