My son, Jesse, has been diagnosed with Scleroderma. We are going through the enrollment process for Dr. Burts' stem cell transplant trials at Northwestern Memorial Hospital in Chicago.
Jesse's only form of insurance is Medicare. Dr. Burts' staff has suggested that we appeal to this forum for information regarding expenses after Medicare. If anyone out there has gone through or is going through a similar situation, please contact us and give us an idea of what we can expect and plan for after Medicare coverage. Thank you for your support. I look forward to any information regarding this topic.