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Thriving with Scleroderma

Lisa Helfand shared her personal journey at the Spring 2015 Scleroderma Patient Education Conference, with a presentation titled “Thriving with Scleroderma.” In case you missed it, the inspirational video is posted below.

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Highlights include:

  • Her long process of a diagnosis. Lisa’s been a scleroderma patient for 30 years. Initially, her scleroderma went untreated for two years and was characterized as warts.
  • Instead of living her life she was told she needed to devote her life to the disease.
  • Dealing with daily pain and the active decision to not dwell on it.
  • You don’t need to be positive all the time. Allow yourself a day to be sad, but take the next day head on.
  • Compassion and advice for anyone living with a chronic illness, particularly scleroderma.

Lisa is not only thriving with scleroderma herself, but wants to inspire others to do the same. In addition to public speaking, she writes a blog, wrote a book and started a campaign called “Face Off for Scleroderma” after she posted a photo to Facebook and it was denied. She encourages others to participate by posting photos sans makeup.

To connect with Lisa and read more of her inspirational posts visit her blog.

Additional tips on thriving with scleroderma:

  • Meditation: Allow yourself to develop a routine to organize your thoughts. Whether it’s yoga, writing a story, or doing breathing exercises, it’s important to do something for yourself.
  • Highs and lows (roses and thorns): This is always a fun interactive game to play around the dinner table or whenever you’re together. Even if you aren’t having the best day, this activity allows you to focus on the great things that happen every day. Believe me, you can always find at least one.
  • Don’t accept depression: There is a strong correlation between attitude and quality of living. If you’re struggling with depression please talk to your doctor, a psychiatrist, or another trusted individual. It’s important to keep your routine as normal as possible after a diagnosis because you and your family feed off each other and need to reciprocate support.
  • Be patient: Find the right doctor for you. It’s important to find a team of doctors that communicate and make you feel comfortable. A diagnosis like scleroderma will not be an easy road and so it’s valuable to have a team that understands not only your disease, but you as well. The Scleroderma Foundation can help provide physician referrals.
  • Support System: Recognize the people in your life that mean the most to you. Everyone has moments of weakness and it’s important to have a strong support system behind you to lift you up when needed.

As Lisa says, “You have three options: give up, give in, or give it all you’ve got!”

 

Source: http://www.niams.nih.gov/Health_Info/Scleroderma/scleroderma_ff.asp

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Scleroderma walk season is upon us!

Looking for a fun way to keep active this summer and enjoy the beautiful weather outdoors? It’s walk season! Come participate in a Stepping Out to Cure Scleroderma walk and help raise money to find a cure!

Our online fundraising tools make it easy to set a fundraising goal, personalize your fundraising page, contact family and friends, and track your progress. Get started today by registering for a walk near you! If you can’t attend, you can still register and help raise money online.

Listed below are the upcoming scleroderma walks and links to register for the event. The more the merrier- so bring your friends and family too!

Walk Schedule:

Stepping Out to Cure Scleroderma- Springfield, IL
Saturday, June 20, 2015

Stepping Out to Cure Scleroderma- Highland Park, IL
Sunday June 28, 2015

Reason to Rock Fun Walk and 50s Fest- Geneva, IL
Sunday, July 26, 2015

A note from the walk coordinator, Marcia Warren: We’re excited about our 2nd Annual Reason to Rock walk on Sunday, July 26, at the Fifth Third Bank Ballpark (home of the Kane County Cougars) in Geneva, IL.  The event has a 50’s theme and starts out with a walk around the track, and then music, food, fun and a classic car show.  We had a great turnout last year and hope you will join us this year to help support the fight against Scleroderma!

Stepping Out to Cure Scleroderma- Germantown, WI
Sunday, August 16, 2015

Stepping Out to Cure Scleroderma- Dixon, IL
Saturday, September 12, 2015

Stepping Out to Cure Scleroderma- Highland, IN
Saturday, September 19, 2015

Put on those walking shoes and we hope to see you out there!

VIDEO: A Look Back at 2014

Thanks to YOU, 2014 was a great year and we are excited to enter 2015 with even more commitment and determination than ever! During this season of giving and reflection, it only makes sense that we give thanks to our supporters for everything you’ve done this year. You are the lifeblood of our organization and the source of hope for so many scleroderma patients. Check out this short video for just a few of the highlights. I hope you will continue the fight with us in 2015, as we work to put an end to scleroderma.

Best wishes,
Stephanie Somers
Executive Director
Scleroderma Foundation, Greater Chicago Chapter

VIDEO: Thanks to YOU! A Look Back at 2014