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The Stevens Johnson Syndrome Foundation (Julie Foundation for allergic drug
reactions) is a non-profit organization. The purpose of the foundation is to
provide the public and medical communities with information on adverse allergic
drug reactions. Our goal is to make the public aware of adverse reactions, so
that a quick diagnosis may be made and the offending drug stopped as soon as
possible.
Allergic drug reactions are the fourth leading cause of death
in the United States [ Read more ].
Adverse Drug Reactions may cause over 100,000 deaths among
hospitalized patients each year [ Read more ]. Less then 1% of all drug reactions are
reported to the FDA. The public needs to know what to look for when taking any
drug and seek medical attention immediately in the event of a reaction in order
to prevent permanent damage. The SJS Foundation is also doing medical research
into SJS/TEN
The Stevens Johnson Syndrome Support Group originated in May of 1995. The
Group's purpose is to provide emotional support for people with Stevens Johnson
Syndrome and Toxic Epidermal Necrolysis.
Stevens Johnson Syndrome/Toxic Epidermal Necrolysis:
Adverse drug reactions.
Painful Blistering of the skin and mucous membrane involvment.
In many cases preceded with flu like symptoms and high fever.
As it evolves the skin literally sloughs off.
Ocular involvement includes severe conjunctivis, iritis, palpebral edema,
conjunctival and corneal blisters and erosions, and corneal perforation.
Almost any DRUG can cause SJS/TEN, including over the counter drugs. SJS
& TEN do not discriminate against anyone! Everyone should be aware of
allergic drug reactions.
Mission Statement The SJS Foundation was founded to be a resource to SJS victims and their families. Our mission is provide support services, and compile and distribute valuable information about SJS to the public and medical professionals regarding treatments and therapies that prove beneficial to SJS sufferers. We work to promote public awareness about the signs of SJS so that a quick diagnosis can be made and the offending drug stopped as soon as possible.
Note:
The Stevens Johnson Syndrome Foundation (The Julie Foundation) is a nonprofit organization established in 1995, dedicated to bringing public awareness and research to adverse drug reactions that cause Stevens Johnson Syndrome (SJS) and TEN (Toxic Epidermal Necrolysis) through the use of prescription and over the counter medications. Since recent Black Box warning have been placed on some medications, we have learned that there may be certain individuals attempting to solicit funds under the guise of The SJS Foundation. The Stevens Johnson Syndrome Foundation is an organization based solely in Westminster Colorado.
Articles or advertisements referring to specific programs, services and/or products do not constitute endorsement by the Stevens Johnson Syndrome Foundation. Articles involving medical aspects of SJS are not intended to be medical advice and readers are cautioned not to make any changes in their treatment based on information without consulting with a physician.
Manute Bol's Death Sheds Light on Rare Skin Condition, Says Tampa Dermatologist [click here 1], [click here 2]
Information for Donors: The Stevens Johnson Syndrome Foundation is a 501 (C) (3) tax-exempt corporation. All donations to the SJS Foundation are tax-deductible. [ Click here ] for Tax information.