Solaris

The Silver Lining

July 31st, 2010 by Dave

New Solaris Silver Liners
One of the most common questions that we hear at Solaris is, “Do you have liners for your ReadyWrap products?” Now, thanks to your input, we’re able to give you the answer that you want to hear: You betcha!

Solaris is proud to introduce our brand new Silver Liners. Designed specifically to be used with compression and therapeutic garments, they’re the perfect addition to a home management program. Our Silver Liners are currently available in Below Knee and Thigh versions and are manufactured with soft, comfortable materials and unique X-Static to provide you with the best feeling and
most effective liner possible.

As an added bonus, from now until the end of the year, a pair of Solaris Silver Liners will be included with every ReadyWrap! For more information or to purchase new Solaris Silver Liners, call us at 888-918-9180 or email us at info@solarismed.com.

Make a Connection

July 30th, 2010 by Dave

While awareness of Lymphedema is thankfully on the rise, there is still a lot that needs to be accomplished – from awareness to treatment and coverage. Now it is as important as ever to reach out and connect with others in the Lymphedema community. Here are two easy ways you can reach out and help this weekend.

1. Join or create a Lymphedema support group (click here for more info). Then be sure to spread the word about it. Tell people you know, talk with your therapist, post a video on YouTube, tweet about it on Twitter, or post it on Facebook or LinkedIn. You can also email it to us (at info@solarismed.com) and we’ll be happy to put it in our monthly newsletter!

2. Support HR 4662, the Lymphedema Diagnosis and Treatment Bill. Click here to see what you can do to help. You can also track the latest progress of the bill here.

Scrub a dub dub

July 30th, 2010 by Emily

Just a reminder to all that when you are returning your tribute garment for an alteration it needs to be laundered first. This is not only to protect all us lovely Solaris employees but also all of our equally lovely customers as well.

Thanks so much!

Farewell, But Not Goodbye

July 23rd, 2010 by Dave

Today was Amanda’s last day and going away party before moving down to Illinois. While everyone at Solaris is sad to see her go, we all wish her the best of luck in her new endeavors (and we’re looking forward to plenty of updates and pictures in the future too)!

Thanks for the good times Amanda!

Solaris Representation in New Zealand!

July 23rd, 2010 by Nicole

We are happy to announce that Cosmac Healthcare has expanded its distribution reach to include not only Australia but New Zealand as well! 

Cosmac Healthcare
P: 61(0)2 9033 7400
info@cosmac.com.au
www.cosmac.com.au/

For medical professionals from New Zealand and Australia, please contact Cosmac if you would like an in-service/in house demonstration of just how these products help patients.

Kissell’s Lymphedema Bill Gains Support from Komen for the Cure, Living Beyond Breast Cancer, Breast Cancer Network of Strength, Colon Cancer Alliance & LIVESTRONG

July 22nd, 2010 by max

For Immediate Release: July 20, 2010
Contact: Haven Kerchner, 704-786-1612
Haven.kerchner@mail.house.gov<mailto:Haven.kerchner@mail.house.gov>

Kissell’s Lymphedema Bill Gains Support from Komen for the Cure, Living Beyond Breast Cancer, Breast Cancer Network of Strength, Colon Cancer Alliance & LIVESTRONG

The Lymphedema Diagnosis and Treatment Cost Saving Act of 2010, legislation introduced by Congressman Larry Kissell to improve treatment coverage for lymphedema sufferers, continues to garner support from national cancer organizations.  H.R. 4662 requires Medicare to offer fair treatment coverage for Americans suffering from primary and secondary lymphedema.
Lymphedema, also known as lymphatic obstruction, is a condition of localized fluid retention and tissue swelling caused by a compromised lymphatic system. Many cancer patients suffer from this condition.
“This is a terrible condition that affects thousands of Americans every day, and yet, many cannot get the treatment they need to improve their quality of life,” Kissell said. “After meeting many folks suffering from lymphedema, I believe this legislation will help dramatically improve their lives. I am grateful so many organizations dedicated to help those who fight cancer support the Lymphedema Diagnosis and Treatment Cost Saving Act.”
The Susan G. Komen for the Cure Advocacy Alliance, Living Beyond Breast Cancer and the Breast Cancer Network of Strength signed a joint letter of support – thanking Congressman Kissell on behalf of breast cancer survivors for introducing the Lymphedema Diagnosis and Treatment Cost Saving Act of 2010.
In a joint letter to Congressman Kissell, Jennifer Luray, President, Komen Advocacy Alliance; Jean Sachs, CEO Living Beyond Breast Cancer; and Kay Wissman, Director of Government Relations for Breast Cancer Network of Strength, stated, “As you know, breast cancer survivors can develop lymphedema as a result of surgery or radiation to the lymph nodes in the armpit. Any woman who has breast cancer surgery and lymph nodes removed is at risk for developing lymphedema, and she remains at risk for the rest of her life. Fortunately, most breast cancer survivors do not get lymphedema. However, the women who do may face considerable pain, reduced movement, serious infections, emotional distress and reduced quality of life.”
The Colon Cancer Alliance has also lent its support to the legislation. “Many cancer survivors suffer from lymphedema following primary treatment. It is vitally important that Medicare cover lymphedema treatment and treatment materials, including compression bandages and garments required for everyday care,” said Andrew Speigel, CEO of the Colon Cancer Alliance.  “The Colon Cancer Alliance is proud to join forces with other cancer organizations in support of the Lymphedema Diagnosis and Treatment Cost Saving Act of 2010, HR 4662.”
Earlier this year, LIVESTRONG, the foundation started by seven-time Tour de France winner Lance Armstrong, announced its endorsement. More than 39 organizations have lent their endorsement to H.R. 4662 including National Lymphedema Network, Lymphedema Awareness Foundation, Carolinas Rehabilitation and NC Comprehensive Cancer Program.
Kissell introduced the legislation after meeting Charlotte constituent Heather Ferguson. Ferguson’s young son, Dylan, suffers from primary lymphedema. After fighting with her insurance company to get coverage for Dylan’s compression bandage treatments, she took her fight statewide. Ferguson worked with North Carolina Representative Tricia Cotham to get legislation through the North Carolina General Assembly before meeting with Congressman Kissell to ask him to take the fight to Congress.
The treatment for lymphedema is known as complex decongestive therapy. This treatment is used world-wide, is not experimental, and has been used for decades with proven success. Not all components of the treatment fall under the categories for which Medicare typically provides coverage. With treatment, patients can live long, healthy and virtually normal lives. However, without treatment, the disease can progressively worsen, causing severe disfigurement, disability, pain and in some cases, death.  H.R. 4662 currently has 39 bipartisan cosponsors.

On the road again: North Dakota/South Dakota and Oklahoma/Dallas area

July 22nd, 2010 by Jason

I am planning a trip to the ND/SD area August 23-27 and visiting the Dallas/Oklahoma area September 13-17. If you are interested in having me stop in, please email or call me. I look forward to meeting with all of you!!

Jason Longmier
P: 414-918-9180
C: 715-577-8778
jason.longmier@solarismed.com

Utah

July 21st, 2010 by Beth

Tying up all of the last minute details for my visit to Utah! I haven’t been to Salt Lake City since college, but remember that I loved it! Looking forward to meeting the area therapists!

About Warranty Information

July 21st, 2010 by Steph

As Solaris’ Outreach Coordinator, I would like to assure all our customers and future customers that the information given to Solaris, Inc. on the warranty cards will NEVER be sold to other companies or used to bother you unnecessarily. This is a Solaris Promise to you. Please feel comfortable to send your card back to us as soon as possible.

If you have any further questions please feel free to contact me by phone at 888-918-9185 or by e-mail at stephanie.gamble@solarismed.com

Have a great day!!

Stephanie

A Bicycle Built for You

July 16th, 2010 by Dave

Whether you love hitting the open road with your pedal-powered two-wheeler or helping make a difference, the Tour de Pink is for you.

Now in it’s sixth year, the Tour de Pink (on Sunday, September 19th) is Texas’ first bike ride event solely benefiting breast cancer education and awareness programs (through the Pink Ribbons Project).

The Tour has almost raised $19,000 already, but still needs your help to reach their goal. Please click here to visit their site for more info and to see how you can help!

Thanks to Kristen Anderson at Ricky Knowles Hair & Wellness for sharing this. If you know of any events in your area feel free to let us know, we’d love to help spread the word!

Have a great weekend!

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