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Jay is a former firefighter and paramedic from Daphne, Alabama, living with Multifocal Motor Neuropathy (MMN). This rare, progressive autoimmune disease interrupts nerve signals to the muscles, with no remission.
Within six weeks of his first symptoms, Jay went from numbness in his hands to becoming a full quadriplegic. His journey back to walking is a testament to the power of exceptional care.
In this video, Jay shares how Soleo became the partner he needed: from a nurse who recognized he was getting sicker and got him back to the hospital in time, to a care team that seamlessly manages his complex infusion schedule so he never has to worry if his medication will be there.
Benjamin grew up with the expectation that hemophilia would define and limit his life. Once told he might not live past 30, he now shares a very different reality. In this powerful story, Benjamin reflects on his journey from being seen as his condition to reclaiming his identity, supported by a care team that treats him as more than a number.
Living in a remote area, access to specialized care wasn’t always easy—but the right partnership made all the difference. With personalized support and innovative therapy, Benjamin has experienced greater stability, fewer bleeds, and a renewed sense of independence.
Watch Benjamin’s story to see how individualized care can transform what’s possible for people living with rare conditions.
Meet Kate Richer, a mother of two from Wauseon, Ohio, who shares her powerful story of living with Graves’ disease and thyroid eye disease, and how home infusion therapy transformed her life.
The constant eye pain, extreme light sensitivity, and swelling made simple daily activities unbearable.
After her thyroid removal surgery, Kate’s doctor connected her with Soleo Health for at-home infusion therapy. This decision became a turning point in her treatment journey.
Kate’s story demonstrates how personalized, compassionate healthcare can restore physical health, quality of life, confidence, and the ability to engage with the people and activities that matter most.
With 35 years in healthcare, starting as a phlebologist and spending the last 15 years as a passionate nurse, Jennifer Grace, BSN, RN, never imagined she’d need the very services she helped provide to her own patients. Her experience with Soleo Health through her practice had been outstanding, but she never expected to become a patient herself.
Jennifer’s lupus journey began at just 16 years old when she woke up with a stiff elbow. In her 20s, the disease nearly claimed Jennifer’s life. In her 30s, lupus went into remission for 13 remarkable years. However, the familiar enemy returned. The signs were unmistakable, but accepting the return of such a life-altering condition was devastating.
Read Jennifer’s Story
Unique was diagnosed with CRION (Chronic Relapsing Inflammatory Optic Neuritis), a rare autoimmune condition where the body attacks the eyes, causing inflammation and potential vision loss.
Initially, Unique was apprehensive about starting IV infusion therapy, her first experience with intravenous medication. The fear of potential side effects led her to delay treatment. However, her neuro-ophthalmologist referred her to Soleo Health for specialized infusion services. Despite her initial fears, Unique found the infusion process far less intimidating than expected.
Read Unique’s Story
Isabella Short is a 27-year-old woman living with Factor X deficiency, a rare bleeding disorder that affects her blood’s ability to clot. This condition requires her to receive infusions three times a week to maintain her health and prevent life-threatening bleeds.
From the beginning, her Soleo nurse provided personalized, attentive care, calling regularly to check on her supply needs, track her monthly bleeds, and monitor any changes in her condition.
Read Isabella’s Story
After 25 years of practicing medicine, Dr. Alan Richmond brings a unique perspective to the patient experience. As someone accustomed to being on the giving end of medical care, adapting to the patient role proved emotionally and psychologically challenging.
Simple daily activities like showering and getting dressed became as exhausting as “running a marathon.” Alan was diagnosed with CIDP (Chronic Inflammatory Demyelinating Polyneuropathy). Dr. Richmond’s initial treatment with high-dose steroids proved to be a nightmare. The side effects dramatically impacted his personal relationships and quality of life.
Read Dr. Richmond’s Story