“If something’s confusing, just ask for help.” That’s the rule in my house. It’s an aide for surviving MdDS. The only problem is, if your brain is foggy then you probably don’t realize you’re confused. That’s how it came to be that I left the car running in a parking lot and walked a couple blocks away […]
The Foundation uses two simple yet effective tools to advocate for you, on your behalf. Upon your request Board President, Marilyn Josselyn, herself will mail out a letter to your doctor that introduces them to MdDS. This one page letter briefly describes MdDS, possible etiology and current research efforts. Click to view a sample: Letter for […]
In the spirit of Giving Tuesday, the MdDS Balance Disorder Foundation would like to share some important news. Over the next year, the MdDS Foundation will be the beneficiary of a directed donation, in the amount of $100,000, with the sole purpose of increasing awareness of MdDS in the medical community and the general population. […]
Through your shares and your kindness, our most important fundraiser of the year is off to a good start. Please help make it great and forward this email. Let your supporters know that Rocking Our Way to $40K is raising both funds and HOPE.
In case you missed these Words of Wisdom on our Facebook page, long-time friend, Abby, shares some great insight in this post. Please read, share, and get those thumbs-up! Please share to show you care! WORDS OF WISDOM FOR FAMILY AND FRIENDS Things people need to know about those suffering from MdDS/MAV/chronic dizziness. By Abby Lane […]
It’s National Volunteer Week! Today we’re shining a light on Breanna by sharing her story and experience with you. Hello, my name is Breanna Larsen and I am a twenty-two year old native Texan who loves spending time with my family and friends, going on adventures, playing with my puppies and trying to spread a little sparkle everywhere I go. […]
MAY 15: The survey is now closed. In an effort to collect current data, a new survey is underway. This survey closes in two weeks, so if you have or suspect that you have MdDS don’t delay — complete the survey. We hope to collect enough data to analyze, and to include key information in the June newsletter. The newsletter […]