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This is MY journey with MS! I give you my thoughts, feelings, hopes, and prayers. My wish that one day this disease will come to an end. That one day there will be a cure. For now, I hold on to possibility. I HOPE this will help and inspire not only myself but others. 7 Digital Divas: Diary of MS X. Bald Ben: Good, Bad and MS. Blinders Off: Living with MS. Carole's MS Blog: The MS Rollercoater, A Ride That Never Ends. Cathy: Navigating the Journey of MS. Chris had MS: An Account of a HiCy Patient". Lisa:...
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I do not wish for anyone to go through this illness, but I would hope that we would all be so blessed to learn the lessons I have at my young age. Please take care of yourselves. I hope you are all well. Tuesday, May 16, 2006. So, Who Am I? My Philosophy: If it won't matter when we are dead, then it wasn't that important to begin with. Tuesday, May 16, 2006. Subscribe to: Posts (Atom). International MS Support Foundation. Montel Williams MS Foundation. MS Complementary and Alternative Medicine.
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Monday, November 20, 2006. Posted by jessikah at 7:58 PM. Sunday, September 17, 2006. Two Things 1. Persepolis: Go out and get this book right now. It's the best way to get a basic overview of Iranian history over the last 50 years- from the point of view of a totally awesome, progressive, rebellious woman. It's autobiographical and really funny, and poignant, even though poignant is a really lame word. Don't worry, this book is not lame. It is educational AND satisfactory! Posted by jessikah at 3:51 PM.
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My MS Journey…. My new journey (with MS). September 22, 2014 in Uncategorized. On a roller coaster this summer. Not a literal one (I hate them, plus I get motion sickness). I started the summer full of ideas. What I would do with my daughter. Day trips and the like. We decided to do a musical together. Footloose! Drove LONG ride home (2-3 hours is really long when fatigue slams you). Quick rest, GNO! Hubby planned a SURPRISE PARTY for me! So more recovery time. Never ending. Moving right along…. My husba...
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Thursday, October 15, 2009. Lorna and the Folsom Ren Fair. Can a mom with multiple sclerosis do it? This weekend is the Folsom Renaissance Fair. MS MOMS has a wine booth there. My husband and caretaker, as well as part time manager, got us this spot. Mark supports MS MOMS and is one of our best fund raising directors. So what’s the issue? Last October and this June I came face to face with a problem that just irks me. I have multiple sclerosis. Eye contact, tone of voice, the way words are phrased, there...
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MS = Mighty Savior! Thursday, May 14, 2015. I have realized I have a lot of fears. That my fear in so many areas influence my life in HUGE ways. I know I need to combat my fears with faith. That even if what I fear happens God is bigger! I feel challenged to do something everyday that I fear. I want to rely on God and not myself. That is how I can see God work in my life and then be used in the life of others. Friday, May 8, 2015. I can't just leave my body on the side of the road! What am I good at?
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My MS, My Story. Thursday, June 18, 2015. Thursday, December 11, 2014. Thursday, October 9, 2014. Time for New Medicine. 10 months since my last post, but there was nothing dramatically changing in my health. To me, this is GREAT news! About a month ago, I received a letter in the mail from my neurologist, Dr. Thomas Diesing. It informed me that he was taking a position at the University of Nebraska Medical Center (UNMC) as the medical director of all hospital neurology services. Good for him! Finally, i...
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