Multifocal Motor Neuropathy

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    Celebrate the small success no matter how small it seems

    “If opening your eyes, or getting out of bed, or holding a spoon, or combing your hair, is the daunting Mount Everest you climb today, that is okay” - Carmen Ambrosio

    I saw this quote and I believe this rings true especially to me personally, to always celebrate any task accomplished as although they may be small they are big to you. Don’t feel belittled by the fact it maybe a “normal” thing to do because today you completed, maybe yesterday you couldn’t and this is something to be celebrated.

    #Fibromyalgia #ChronicFatigueSyndrome #Epilepsy #MentalHealth #MajorDepressiveDisorder #MultipleSclerosis #ChronicIllness #Depression #Anxiety #PTSD #MightyPoets #MightyTogether #EhlersDanlosSyndrome #Lupus #Cancers #CheckInWithMe #RareDisease #MultifocalMotorNeuropathy #Disability #RheumatoidArthritis #PolycysticOvarySyndrome

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    16 Reasons You Should Pay Attention to Rare Disease Day

    Do you know someone living with a rare disease? Seeing as approximately 30 million Americans have one of the 7,000 diseases considered “rare,” odds are, you do. With so many individuals and families affected by rare diseases, you might imagine an abundance of medical resources and support communities exist, but it’s quite the opposite. The National Organization for Rare Disorders (NORD) reports that for most rare medical conditions, no cures and few proven treatments are available, and many people affected by rare diseases have revealed they feel alone and struggle to explain to others what they’re going through. Rare Disease Day is held on the last day of February every year to raise awareness, and this year, The Mighty teamed up with NORD to ask our Facebook communities what those 24 hours mean to them. Here’s what they had to say: 1. “Rare Disease Day is a day I feel acknowledged.” —Asdruval Melissa Cifuentes 2. “A chance that just one more person will become aware of adrenal insufficiency, which means one more person may help save my life.” —Lisa Anderson 3. “Rare Disease Day is a day where people can see this and realize the hardship of fighting something you know nothing about.” —Sumathy Lal 4. “A time [for] the parents who search for answers to the unknown.” —Diane Anderson 5. “Hope.” —DeAnna Wry 6. “A day where the world stops and listens to what the rare community has to say … It’s our chance to create huge awareness and to show that having a rare disease is not that rare.” —Geraldine Renton 7. “It means showing that statistics aren’t always right.” —Lizzie Dicamillo 8. “Rare Disease Day means advocating for my children.” —Olivia Howard 9. “It means appreciating and acknowledging the rare disorder(s) that make me, me.” —Keira Baccei 10. “Rare Disease Day for me is every day! It is just every minute of every day and pushing through ’til the next minute the next day… the next week, month, year, and to just hold on to hope!” —Mellonie Swinford 11. “Rare Disease Day means one day where no matter what the numbers say, no matter how much I may be struggling, no matter how helpless those around me might feel, I am not alone.” —Amanda Leslie 12. “Sadness… since Margarita Day or Pizza Day will have more shares than Rare Disease Day. Sadness, that it takes having a rare disease or having someone close to you with a rare disease to even know this day exists.” —Suzanne Depaolis 13. “Separately each rare disease and their supporters are small in numbers, but together we are a large group of strong and mighty advocates.” —Amanda Buck 14. “One day, there will be a cure for all of us and no one will have to suffer.” — Meghan Bayer 15. “Rare Disease Day gave me the courage to share my story on Facebook, to put it out there to people who may have never have known of MMN [multifocal motor neuropathy].” —Brenda Weisbrod Perales 16. “Rare Disease Day means my child becoming part of a larger community of voices showing how beautiful rare is.”—Miriam Gwynne What does Rare Disease Day mean to you? Let us know in the comments below.