Patient Services
Patient Advocacy
Dr. Sohail Masood, Founder of Dysimmune Diseases Foundation (DDF), has been a patient advocate for more than 30 years. In the late nineteen eighties, Dr. Masood worked with neurologists who diagnosed and treated neuromuscular diseases. At the time, there were an extremely limited number of drugs available to treat these diseases. Dr. Masood worked closely with neurologists who pioneered intravenous immune globulin (IVIG) treatment for neuromuscular disease. These efforts helped generate the development of safer and more effective IVIG formulations than previously available to patients.
When IVIG was not initially an approved treatment for neuromuscular diseases, Dr. Masood advocated diligently on behalf of neuromuscular and dermatological patients to receive IVIG treatments. Over the last 30 years, Dr. Masood has been instrumental in changing the medical guidelines and insurance policies of Blue Cross, Blue Shield, Medicare, Medicaid, and others to provide appropriate insurance coverage for IVIG-treatable diseases. Specifically, he advocated to have CIDP, Myasthenia Gravis, and Pemphigus Vulgaris approved for coverage by Medicare, Medicaid and various commercial insurance companies.
As the owner of Crescent Healthcare, Inc. in the 1990s, when there was a severe shortage of IVIG, Dr. Masood donated IVIG to the National Institute of Health (NIH) so that trials for Stiff Person Syndrome (SPS) could be completed. This trial remains the only placebo-controlled, double-blind study that demonstrates treatment efficacy for SPS.
DDF works to further the passion of its founder, Dr. Sohail Masood, to support patients with dysimmune diseases through advocacy and research funding. DDF continues to advocate for patients’ access to affordable and effective treatments through governmental and commercial channels. DDF is establishing a fund to help patients with financial hardship afford the treatments they are prescribed. At DDF, we continue to embrace innovative ways to make a difference for patients with dysimmune disease. If you have an idea that would help DDF make meaningful changes in patients’ lives please let us know.
Support & Resources
Below you will find a list of support groups and resources for specific autoimmune diseases.
- American Academy of Dermatology
- Alzheimer’s Association
- American Academy of Allergy Asthma and Immunology
- American Academy of Dermatology
- American Academy of Neurology
- American Medical Association
- American Psychiatric Association
- GBS/CIDP Foundation
- Infusion Nursing Society
- IPPF-International Pemphygus & Pemphygoid Foundation
- KabaFusion Home Infusion Therapy
- Medicare Administrator
- Muscular Dystrophy Association
- Myasthenia Gravis Foundation
- National Multiple Sclerosis Society
- National Organization of Rare Disorders
Frequently asked Questions
Below are quick answers to some of our most frequently asked questions.
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What is dysimmune?
“The word dysimmune refers to a dysfunctional immune system. This term encompasses immune system dysfunction and includes immune deficiencies and autoimmune diseases. Dysimmune diseases include immunodeficiencies, neuromuscular, dermatologic, and rheumatologic diseases. -
What is Dysimmune Diseases Foundation(DDF)?
DDF is a non-profit 501(c)(3) organization established to support and promote quality patient care through dysimmune disease patient advocacy and support for research into the cause, treatment, and cure of dysimmune disease.
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How can I reach the DDF?
Click here! -
How can I donate?
All donations to DDF are tax-deductible. You can donate using a credit card, PayPal account, or an electronic check. All options are secure transactions, and your information will not be shared with anyone.