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You can fundraise to help cover the high ongoing costs of living with chronic regional pain syndrome (CRPS).
A diagnosis of chronic regional pain syndrome (CRPS) can turn life upside down, bringing not only persistent pain but also a range of financial challenges. From specialized treatments and medications to adaptive equipment and daily living expenses, the costs quickly add up, leaving many people searching for ways to manage the financial strain.
This post explores different ways to seek financial assistance and support to help manage the costs of living with CRPS.
Living with CRPS can involve significant long-term expenses, as managing pain and preserving quality of life often requires a multidisciplinary approach.
While individual expenses vary, the average annual cost for CRPS in the U.S., including therapies, medications, and interventions, is highest in the 1st year of diagnosis, with median total expenses around $8,500 and prescription costs about $2,000. In the years following diagnosis, annual costs stabilize at approximately $3,900 to $4,800 per year, even before factoring in indirect costs like lost income or transportation.
Insurance coverage for CRPS treatments is unpredictable and frequently incomplete.
Treatment for CRPS may involve prescription pain management, nerve blocks, spinal cord stimulation, physical and occupational therapy, mental health counseling, and adaptive support for daily living – and not all associated costs will be fully covered by insurance.
Many health plans may partially cover certain therapies or physician visits, but significant out-of-pocket expenses for medications, pain interventions, psychological support, and adaptive equipment are common.
High deductibles, copays, and non-covered or “experimental” treatments can place a heavy financial burden on those with CRPS and their families.
Managing CRPS often means facing a wide array of financial challenges, such as:
Every individual living with CRPS experiences unique challenges, and unique care costs. As chronic pain management strategies and advanced treatments become more accessible, securing robust financial support is often essential to accessing the best care and maintaining quality of life.
Starting a fundraising campaign with Help Hope Live is simple and supportive. Here’s how it works:
The fundraising process with our nonprofit starts with a few simple steps:
Help Hope Live differs from GoFundMe by:
We are a nonprofit with more than four decades of fundraising experience and a 4-star Charity Navigator rating.
Yes! We have helped thousands of people successfully cover crucial medical expenses and related costs through our non-profit, Help Hope Live. Here are just a few of their stories.

Liz Barnett has been living with complex heart issues since birth. Once she was listed for a dual heart and liver transplant, Elizabeth turned to Help Hope Live to fundraise for overwhelming out-of-pocket medical expenses. With personalized fundraising support from us, Elizabeth raised $14,000 in less than four months.
At 28 years old, Patrick “PJ” Kent experienced aches and pains that led to a completely unexpected medical diagnosis: acute lymphocytic leukemia. With over $24,000 raised in PJ’s honor with Help Hope Live, fundraising became a critical and successful part of his family’s plan to assist with urgent needs ranging from specialized treatments to inpatient care and unexpected hospitalizations.
If you choose to fundraise with our nonprofit, here’s how the process will look:
1. APPLY for assistance
2. YOU’LL BE PAIRED with a Client Services Coordinator
3. YOUR COORDINATOR will provide you with one-on-one fundraising help, including personalized fundraising materials and guidance on how to rally your community, share your story on social media, reach out to the press, plan in-person or virtual fundraising events, and more.
Need Other Financial Help Options?
For alternatives to fundraising, you can find information on a variety of other financial assistance options. Please view our Catastrophic Illness Resource Directory for insight into sources of direct financial aid, support groups, and other resources for spina bifida patients and their families.