Janis Dadoly

New England | Kevs Core Four

Hello and Welcome! Thank you for visiting Team- KEVS CORE FOUR. Trust me when I say my kids and I are my husbands BIGGEST Fans. If you have the pleasure of knowing Kevin, you will know this is a real club.

Kevin is a role model to many, a teacher, an artist, a comedian, the “BEST Dad ever” he can make you laugh even when you forget how. He always knows what to say. He is the Superman that’s got your back and never expects anything in return. He is very wise and has a heart of gold. And get this! He is so well liked he went and became a Justice Of the Peace so he could wed family and friends who asked! This guy is unreal. (See! The fan club thing is real! Told you!)

With helping others always on his mind I’d like to share his story he shared on his Facebook page below...

“Posting here is not something I do very often, but this post is important to me. I want to share an important health issue I have been dealing with on the off chance it may help someone else.

For more than the last few months I have been having a difficult time speaking. The words are ready but the mouth will not cooperate. Eventually eating and swallowing also became very difficult especially at night. Further at times my speech became like I was very, very intoxicated. Add to this physical exhaustion.

Also on occasion my left eye would droop. Later the droop would go away. While all of these symptoms seem like the signs of a stroke, I was always clear headed and aware of what was happening.

An MRI showed no mass and no tumors. All the doctors spoke of ALS. Thankfully those tests can back negative.

What came back positive was a test for Myasthenia Gravis. This rare condition is treated with medication, which I started today. One of the causes of this can sometimes be a tumor in the chest. Which I am being tested for soon. (This tumor is benign.)

So my journey continues. I was initially diagnosed and treated for a sinus infection. Please keep this story in mind in case you hear of someone with similar symptoms. It has been a long few months and not once did Myasthenia Gravis get mentioned until I saw my neurologist.

The medicine is suppose to relieve the symptoms. I need to talk, I have so much left to say!” -Kevin Dadoly

My kids and I are proud to be supporting the MGFA) through the MG Walk. The MGFA is the only national volunteer health agency in the United States dedicated solely to the fight against myasthenia gravis.

MGFA is committed to finding a cure for myasthenia gravis and closely related disorders, improving treatment options, and providing information and support to people with myasthenia gravis through research, education, community programs, and advocacy.

Please join our team and register to walk with us OR make a pledge to help us reach our goal!

Thank you,

Janis, Taylor & Travis 

Raised: $730
Goal: $150
100 percent raised


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#123  National 
#11  Local

Thank you donors
Janice Mercuri Grossman : $25
Wow! So much to process, but through your love you will walk it one step at a time, I am confident! Holding you in Peace, Jan
Laura Flanagan Chandler : $100
Therese Demag : $50
kathy orbenhall : $25
Andria Hines : $50
Rayne MacGeorge : $35
Thank you for passing this on!
Judy Brown : $50
I'm with Team Dadoly all the way!
Karen Lapierre : $25
Go Dadoly's!! Much love to you all!!
Alison Goodwin
A well deserved donation
Brianna Green : $50
Kevin Eagan : $100
Good luck. We would join you but will be away that weekend. Hugs to Kevin. Karen & Kevin Eagan
Kyle Melvin : $50
Love, Kyle and Meg
Kevs Core Four
Taylor Dadoly - $730 raised
David Brown - $0 raised
Dora Brown - $0 raised
Elizabeth Brady - $10 raised
Ethan Carter - $65 raised
Janis Dadoly - $730 raised
Jeffrey Targ - $0 raised
Jes Carter - $250 raised
Jodi Darrin - $0 raised
Kevin Dadoly - $6206 raised
Kevin Ryan - $305 raised
Kristi Miller - $50 raised
Shannon Douglas - $100 raised
Travis Dadoly - $2205 raised

Join this team