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My MS infusion journey

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Some of you know me and some don’t, I have multiple sclerosis and was dx’d in May of ‘92….its now 2023 and I’m still fighting just to keep it at bay, over the years I have tried numerous medications to try and slow down it’s progression (tried 7 different medications now onto #8) praying this one does because only other option is Stem Cell Transplant
I’m not a quitter and will never give up but this disease has taken soooo much from me already and I’m running out of ways to adapt and modify daily not to mention this disease is extremely COSTLY
As of today 12-17-2023 I’m trying a new infusion medicine for 5 days straight here at Stanford Nescience Facility in Stanford. My neurologist is hopeful that this medication will slow it down, until then I’m hooked up and infusing for 5 days straight for 8 hours (yes 8 hours) and due to many different complications my husband is having to drive us back and forth daily. Very costly plus he’s having to take off work until the new year begins due to possible complications for me so if anyone can help offset extra expenses we may or may not be able to afford I’d be ever so grateful.
thank you all, God Bless and Happy Holidays
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Donations 

  • Anonymous
    • $100
    • 1 yr
  • Mark Leigh
    • $500
    • 1 yr
  • Tami Fournier
    • $100
    • 1 yr
  • Barbara Ward
    • $25
    • 1 yr
  • William van Vliet
    • $100
    • 1 yr
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Organizer

Kim Pierce-Suffecool
Organizer
Merced, CA

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