User Tag List

Likes Likes:  0
Page 1 of 61 1231151 ... LastLast
Results 1 to 10 of 601

Thread: From undiagnosed to climbing Mt. Everest!

  1. #1
    Join Date
    Nov 2009
    Location
    California, USA
    Posts
    284
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default From undiagnosed to climbing Mt. Everest!

    Hi Everyone,


    Reaching Beyond the Clouds: Mt. Everest


    For some time I had been experiencing a variety of unusual physical problems (i.e., in 2003, I had to have sinus surgery). However, the problem that concerned me most was my rapid loss of vision. I went to many medical specialists and had many tests preformed, but the cause of my symptoms remained a mystery. Setting aside the other physical problems, I focused on saving my vision. I believe I can handle just about anything, but I was terrified of going blind. Enter Dr. Holland of Jules Stein Eye Institute at UCLA: An amazing doctor who worked tirelessly to save my deteriorating vision. Dr. Holland diagnosed me with retinal vasculitis.

    After watching an amazing Discovery Channel show called Everest: Beyond the Limit, I was drawn to climb that mountain: the beauty, the challenge. Please realize that at the time I had climbed only Mt. Kilimanjaro and was no mountaineer. So, at the age of 48, I was going to start training for a new adventure: mountain climbing. Subsequently, I contacted Scott Woolums, a very experience high-altitude guide, and we made arrangements to climb Mt. Aconcagua in Argentina (the highest mountain in South America) for our first training climb.

    Then it happened! While shopping at a local nursery I was overcome with vertigo and realized I could not see out of my left eye: a retinal vascular occlusion. After reviewing test results, Dr. Holland and Dr. Kreiger (Jules Stein Eye Institute, UCLA) referred me Dr. Gorn a rheumatologist at UCLA Medical Center. On August 1st 2007 I was diagnosed with Limited Wegener's Granulomatosis. As shocking as that was: At least now I knew what I had and began a medication treatment program.

    Two weeks later I was admitted to the emergency room having TransientIschemic Attacks (TIA - mini-stokes). OK, more medical tests and doctors check-ups: but I keep moving toward to goal of climbing Mt. Everest. As many of you know, the medication(s) to treat WG have side-effects and can make you very ill: which, for me, lasted for many months. I continued training – I have a mountain to climb!

    Four months later, we went to Argentina and climbed Mt. Aconcagua. Unfortunately at 20,000 feet we had to abort our summit attempt due to very high winds. On the way down, around 19,000 feet, I snagged my boot on the other boot, fell, and broke my leg: but I still had to hike 5 hours down to base camp because we were too high for helicopter evacuation. Over the next 7 months I had a couple of surgeries (plate in/plate out) and continued on – I have a mountain to climb.

    This past Summer, with the love and support of my wonderful husband of 18 years, we summited Mt. Rainier, 14, 410 ft; summated Mt. Elbrus, Russia, 18, 513 ft; climbed Peak Lenin, Kyrgyzstan, to 22, 500 ft, we had to abort summit due to team member getting frost bite.

    Currently, I am in remission due to a continuous medication treatment. Fortunately and unfortunately, the medication suppresses my immune system thus putting me at a risk high infection. If I stop taking the medication, however, the disease can continue to damage my body. Most obviously, the disease is attacking my eyes and I am functionally blind in one eye, but (for now) we have saved my other eye.

    I am a 50 year old female who teaches Health Science at California State University, Fullerton.

    I leave for Kathmandu on April 1, 2010 for the 70 days it takes to prepare for and climb the South Side of Mt. Everest. The fact that I have Wegener's Granulomatosis does not change my drive to live life to its fullest and that is exactly what I plan to do!

    For more on my story go to my climbing/fund-raising blog at
    www.reachingbeyondtheclouds.com

    I will be climbing to raise Rare Disease Awareness and money for the Vasculitis Foundation for research and support services.
    Last edited by Cindy; 11-08-2009 at 08:27 AM.

  2. #2
    Doug Guest

    Default

    Wow! What else is there to say? (Being me, however, I'll continue on, and on anyway!) Very inspirational. We emphasize a positive attitude on this site, and you exemplify it. I'll try to get on your blog again after I finish on this site. My computer is running slow today, so I probably will have to work on that first. Anyway, thanks for posting your story! I'm going back to the top again, it's so good! I hope you can post us from Nepal when you do the big climb, or at least tell us about it later.

  3. #3
    Join Date
    Nov 2009
    Location
    California, USA
    Posts
    284
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Hi Doug, Nice to meet you. I will be able to post from Everest base camp but only to my climbing blog. My hope is that I will get media attention during the climb so people will donate to the Vasculitis Foundation to raising money for research!
    Last edited by Cindy; 11-08-2009 at 07:58 AM.

  4. #4
    Join Date
    Nov 2008
    Location
    Maryland, USA
    Posts
    10,836
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Cindy, so you didn't have lung or kidney involvement?

  5. #5
    Join Date
    Nov 2009
    Location
    California, USA
    Posts
    284
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Sangye,
    Well, I have blood in my urine (mild to moderate) but (so far) no lung involement. I have several issues with the WG stuff and taking the meds at extreme altitude is tricky but so far I have been able to stay on my training schedule: some days are better than others - as we all know.

  6. #6
    Join Date
    Feb 2009
    Location
    Saint Peter, Minnesota
    Posts
    460
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Wow! Cindy,

    I am impressed and inspired. I believe in your "live life to the fullest" statement, but I have not had the courage to venture to the levels you have. I am very impressed. Please keep us informed....for inspiration if nothing else.

    Lisa Coffeelover

  7. #7
    Doug Guest

    Default

    My cat can beat your panda....! No, once again I commend you for your remarkable spirit and daring do.

  8. #8
    Join Date
    Nov 2009
    Location
    California, USA
    Posts
    284
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Lisa: Thanks I have always followed my dreams to experience and explore everything! Check out some pictures I posted in my photo album. I do not think of it as courage - more like tenacity. After being disgnosed with WG I decided that I was going to be in control of my life: not the disease!

    Doug: Ha-Ha, that panda could have ripped my face off! I was at a panda research center in China. I have cats - they also type on my keyboard (so helpful).

    Just got home from hiking Mt. Baldy - time for a nap

  9. #9
    Join Date
    Nov 2009
    Location
    California, USA
    Posts
    284
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Can I ask you all a favor? If you visit my blog would you leave a comment about your story or the need for research etc... I am in the process of trying to get California to recognize Rare Disease Day (Feb 28th) and your comments would help the Governor see that WE ARE OUT THERE and need special legistation for our awareness so we can get diagnosed, special treatments, medications, and services.

    www.reachingbeyondtheclouds.com

    Thanks!
    Last edited by Cindy; 11-09-2009 at 11:31 AM.

  10. #10
    Join Date
    Apr 2009
    Location
    South Carolina
    Posts
    4,273
    Post Thanks / Like
    Mentioned
    0 Post(s)
    Tagged
    0 Thread(s)

    Default

    Cindy like you I have left eye pain for years, went to about 8 different eye docs and said it was dry eyes. Finally I was diagnosed last year and they are doing a cat scan of my orbitals tomorrow. Your a great inspiration! The disease and medications can be a bit challenge and its so good to hear your great positive attitude.

Page 1 of 61 1231151 ... LastLast

Bookmarks

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts
  •