We Have MS Too

06/22/2024

Zoom meeting date for this month is set! We invite all We Have MS Too warriors to join us as we touch base amidst these busy summer months🧡

https://forms.gle/JKfSFRnKzJXqas767

05/31/2024

A very happy World MS day from We Have MS Too! I wanted to post this picture from our most recent meeting in honor of today to recognize these intelligent young advocates for the MS community. One of the main topics of discussion this meeting was observation and its importance as a caregiver, especially moving into these summer months. Wishing all the best 🧡🧡🧡

05/21/2024

May date is here! If you are a child affected by the MS diagnosis of a loved one, please join us. Please like, share, comment. Use this link to sign up.

https://forms.gle/XgfBzznUMCLwfJi59

05/12/2024

Wishing a very happy Mother’s Day to all of our We Have MS Too moms! To both those afflicted and those that are caregivers, we are incredibly grateful for your hard work and support; this journey would not be possible without you guys. You all have raised incredible and intelligent kids who have each played a huge role in We Have MS Too’s development. I hope everyone is able to connect with those loved ones on this special day🧡🧡🧡

04/26/2024

Mom Takeover! Introducing myself and telling y’all about the April Zoom meeting.

04/15/2024

April date is here! If you are a child affected by the MS diagnosis of a loved one, please join us. This month we welcome parents. Please like, share, comment. Use this link to sign up.

https://forms.gle/WcY4nuyj7Aq2ytXd8

04/06/2024

It’s here! The MS walk is tomorrow am. We are very thankful for all the support our team, We Have MS Too, has received. The program starts at 9:50 with the walk starting at 10. Let’s meet by the stage at 9:40. It’s not too late to join us.

You can help support groundbreaking research, provide life-changing services and guarantee a supportive community for those who need it most. Please support me with a donation to Walk MS to help create a world free of MS!

03/24/2024

Introducing Mrs. Michaela Pohl! Michaela is a wife, a mom of two young kids, a grief and loss mental health therapist, and an adult child of a parent with MS.

Her mother was diagnosed with Primary Progressive MS almost 35 years ago, soon after Michaela was born. Her mother’s MS greatly affects her mother’s mood, her physical abilities, and her cognitive abilities. When Michaela was a freshman in high school, her maternal aunt died from complications of MS and this is when Michaela learned about her mother’s MS and her role as a co-caregiver began. Michaela is grateful for MS Youth Camp where she met other teens navigating being a teenager while also being caregivers to their parents with MS.

In honor of MS Awareness Month, we will be hosting Michaela in our March meeting as a guest speaker! I highly recommend any warrior who is able to to join. Michaela 's experiences both working with children of MS and being a child of MS make her an incredible resource for this organization. Be sure to come ready to learn about a new perspective, ask questions, and draw connections!

03/18/2024

An honor and privilege to be hosted on the “We’re more than MS” podcast! The host, Mayteé is a strong advocate for multiple sclerosis awareness and hosts a variety of successful people on her show, each with their own unique connection to the disease. This is a group I am grateful to be a part of. Mayteé, like my mom, is a mother with MS. Her children are also very intelligent about the disease; I had the opportunity to speak with them during our most recent meeting. If interested in learning more about either of our stories, this episode can be found on both YouTube and Spotify 🧡🧡🧡

03/13/2024

March date is here! If you are a child affected by the MS diagnosis of a loved one, please join us. Please like, share, comment. Use this link to sign up. https://forms.gle/3EKMtRZHGw5nkSjy9

02/29/2024

🚨ATTENTION WARRIORS🚨
I’d like to take a moment to brag on the new faces I had the privilege of meeting Tuesday night during our February meeting. We came from different age groups and places but I was thoroughly impressed by each member’s insight on their condition.
Secondly, I’d like to give kudos to warrior Emma Taylor for this idea. She proposed a We Have MS Too GroupMe as a convenient way for members to keep in contact. On the QR code is a link for all warriors to join. I encourage everyone to join as it provides a great platform to learn about others’ stories outside of the meetings.
Happy Spring 🧡🧡🧡