Comments for ziMS Foundation - founded by Ryan Zimmerman

Comment on Ryan Zimmerman holds event at Nationals Park in fight against multiple sclerosis by Ryan Zimmerman holds event at Nationals Park in fight against … | vedecugom

Sun, 10 Jul 2011 04:31:27 +0000

[...] Source: http://zimsfoundation.org/news/news/ryan-zimmerman-holds-event-at-nationals-park-in-fight-against-mu... [...]

Comment on Face of Franchise, Zimmerman Is One Attractive Selling Point by Francis

Francis — Thu, 14 Apr 2011 07:04:42 +0000

Yeah, cool decision from Zimmerman, and of course a good player

Comment on Ryan Zimmerman’s “A Night At The Park”–A ziMS Benefit Event by admin

admin — Thu, 07 Apr 2011 21:39:32 +0000

Hi Larry, the Night at the Park event is currently TBA. We will post more information about this years event as soon as we firm out the details.

Comment on Cheryl Zimmerman and Her Family by Dr. Debbie Heil

Dr. Debbie Heil — Thu, 07 Apr 2011 02:42:14 +0000

Hello Ryan…
During this evenings Marlins/Nationals game, my husband Dr. Alan Galbut caught a tidbit about your foundation and that your Mom has been battling MS. He immediately googled it and was impressed by what you are doing for people with Multiple Sclerosis.
I consider myself to be a “Real Expert Living with MS” since my diagnosis nearly 20 years ago. My 1st charity MS Home—now the MS Center of SWFL that I cofounded in 2000 with my fellow MSer Lisa Luthringer RN, MSN provides Wellness Services (Massage Therapy, Acupuncture, Physical Therapy, Equine Therapy, Aqua Therapy) to individuals afflicted with MS. While we are all waiting for a CURE, we must learn to embrace this devastating disease and continue to LIVE. Survival is dependent on adaptation and accommodation. In 2007 Lisa & I cofounded our 2nd charity the HEIL LUTHRINGER FOUNDATION for MS Education to provide critical knowledge to MS patients, their families & caregivers and the medical community. Please let me know if I can be of assistance to you and your organization. I would be happy to share my expertise and give encouragement to your Mother and others struggling with MS.
Together we can make a difference!!!
With hope, love & faith…
Dr. Debbie Heil
Naples, Florida

Comment on Ryan Zimmerman’s “A Night At The Park”–A ziMS Benefit Event by Larry Kropp

Larry Kropp — Thu, 24 Mar 2011 18:54:16 +0000

Please send me info for this years event. Thanks.

Comment on Cheryl Zimmerman and Her Family by Scott Smith

Scott Smith — Wed, 09 Mar 2011 21:16:50 +0000

Keith, Cheryl & Family:

After reading this, I was moved. But knowing many members of your family from the 1970′s in PVHS, this commentary has really hit home in my heart. What has touched me is the bravery shown in your everyday lives; all of you. Both the Zimmerman & Wallace families have always been very proud, grounded and athletically gifted (from Scott Wallace & Keith’s basketball days, Cheryl’s field hockey & basketball, Craig’s skateboarding, etc.) clans. This obviously has carried over through your lives and into your children’s lives. My thoughts and prayers are with you.

Comment on Cheryl Zimmerman and Her Family by Carrie Latham

Carrie Latham — Mon, 28 Feb 2011 20:33:03 +0000

Allow me to introduce myself. My name is Carrie Latham and I am the team captain of Carrie’s Crew. Our team has walked for 7 years for the National Multiple Sclerosis Society – Hamptong Roads Chapter. In these years we have become more and more successful each year raising money with various fund raising events. Two years ago we were awarded the Gold Member award for raising over $3500.00!

This charity is super important to me because I was diagnosed 11 years ago with MS. This disease can be very unpredictable and you never know when a “flare up” will occur, as you know. I’ve had it effect my mobilization and my eye sight. Although I am very grateful for the fact that there are medications to help detain the disease, there is still not a cure. For the past 11 years I have been injecting my medicine every other day. I long for the day when there will be a pill form of medicine or even better, A CURE!!

The Carrie’s Crew Golf Outing will occur this year on June 3, 2011 at Stumpy Lake Golf Course. I hope that I can count on your support. With the unpredictability of this disease, those of us who are living with it need to do what we can, while we can.

This event is in conjuction with the MS Walk that is occuring on April 10, 2011. My husband decided to plan this event and we’re just reaching out to anyone and everyone trying to raise as much money as possible for a cure that is so important to us. Any kind of support from ziMS would be GREAT! Whether it be items for raffle baskets/door prizes or donations, please know that it will go towards a cause that is important to both of us. I’d also love to send you a copy of the sponsorhip flier as well.

For you guys as children of a parent who has MS, it helps me to know the difficulties that my children may be facing as they live with me. Thank you for posting this blog.

Thank you in advance for you time. Should you have any questions, please feel free to contact me at 757-644-9202.

Comment on Ryan Zimmerman Wins Web Gem Award by Mathew Sisson

Mathew Sisson — Fri, 04 Dec 2009 13:44:42 +0000

UZR/150 is over 150 defensive games played, not innings. Easy mistake to make…

Comment on Zimmerman’s Virginia Competitor by admin

admin — Wed, 02 Sep 2009 15:55:05 +0000

This is Pretty Cool.