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FEATURE | BROATCH<br />

We are acutely aware of the devastation caused by the pain of CRPS.<br />

People become disabled and marriages fail. Families break part and lives<br />

are financially ruined. People become socially isolated and housebound.<br />

CRPS, Social Security, Workers’<br />

Compensation, and the Insurance Industry<br />

Although it is a challenge for most people who apply for Social<br />

Security Disability benefits, individuals with CRPS are hampered<br />

by the lack of knowledge and understanding of the syndrome<br />

itself. In 1999, RSDSA was instrumental in convincing<br />

the Social Security Administration to issue a special ruling on<br />

how to adjudicate CRPS claims. We continue to receive letters<br />

RSDSA Publications<br />

and email from members<br />

who have used<br />

our information to get<br />

their claims approved.<br />

Injured employees<br />

with CRPS do not fare<br />

well in the Workers’<br />

Compensation (WC)<br />

program. Of the 1,362<br />

people who completed<br />

the web-based survey,<br />

41% reported being<br />

injured at work; however,<br />

only a few of<br />

them obtained workers’<br />

compensation benefits.<br />

Too often, the<br />

relationship between<br />

an injured worker and<br />

the WC insurance carrier<br />

erupts into a war.<br />

Treatment is frequently<br />

delayed and denied.<br />

In 2005, RSDSA<br />

exhibited at the conferences<br />

of two major workers’ compensation groups, the<br />

Risk and Insurance Management Society and Case Management<br />

Society of America. We view these conferences as opportunities<br />

to reach out to case managers and risk managers,<br />

some of whom still view CRPS as a nebulous, expensive,<br />

and frequently fraudulent claim. We launched a special newsletter,<br />

Working Together, Ensuring a Brighter Future, at these conferences.<br />

Our goal is to develop a mutually beneficial<br />

relationship. We will distribute our new Clinical Practice Guidelines<br />

to the insurers to encourage early intervention and appropriate<br />

treatment, enabling individuals with CRPS to recover<br />

and return to work.<br />

RSDSA publishes several free brochures to help people with CRPS/RSD, their families, and their healthcare<br />

providers. Please call RSDSA at 877-662-7737 to order copies.<br />

In Pain, Out of Work, and Can’t Pay the Bills, a resource directory, contains information on government programs, patient<br />

assistance programs, insurance, community and faith-based sources of help, resources for veterans, and much more.<br />

Recognizing, Understanding, and Treating CRPS/RSD is a quick overview of the syndrome, its telltale signs and symptoms,<br />

and treatment ideas. It is particularly valuable for those people who are newly diagnosed and their families.<br />

Helping Children with RSD Succeed in School is a practical guide for parents, teachers, school nurses, and administrators<br />

on accommodating the school environment for children and adolescents who have CRPS/RSD.<br />

Treating Complex Regional Pain Syndrome/<strong>Reflex</strong> <strong>Sympathetic</strong> <strong>Dystrophy</strong> Syndrome, A Guide for Therapy contains<br />

information on evaluation of CRPS/RSD for functional rehabilitation, treatment protocols, and treatment progression.<br />

CRPS/RSD and Sports Injuries: Prevention is the Name of the Game addresses the risk that athletes have of developing<br />

the syndrome. New research also links the development of CRPS to some of the surgeries that have traditionally helped<br />

sports injuries. This brochure is a must-read for athletes, parents, coaches and athletic trainers, as well as those who<br />

practice sports medicine.<br />

Telltale Signs & Symptoms Handicard is a quick reference for practitioners. The laminated, credit-card size card features<br />

the telltale signs of CRPS on one side and a pain scale on the other. This tidy handout has been a great hit among<br />

healthcare professionals, students, and people who have CRPS/RSD.<br />

Patient Education<br />

Linda Lang, an RSDSA board member and coauthor of Living<br />

with RSDS, described the tremendous losses experienced by an<br />

individual with CRPS.<br />

What to Call It —CRPS or RSD?<br />

IN RECENT YEARS, the medical community has almost universally accepted the term Complex Regional Pain<br />

Syndrome Type I (CRPS) to describe what had been called <strong>Reflex</strong> <strong>Sympathetic</strong> <strong>Dystrophy</strong> Syndrome (RSD). CRPS is<br />

a more comprehensive term that denotes the syndrome’s regional nature and that it is not always mediated by the<br />

sympathetic nervous system. For this magazine, we used whatever term the author chose (CRPS, RSD/CRPS, or RSD).<br />

18 | T H E PA I N P R A C T I T I O N E R | S P R I N G 2 0 0 6

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