[Click here: YouTube - Channel]. I am a proud parent of two teenagers. I am a social worker for adults with mental disabilities that I find very rewarding. I recently was very ill with Steven Johnson Syndrome. I am still in the healing process but I am almost there! Thank God!!! It has been a long road. I am here on YouTube to find or create a support group regarding Steven Johnson Syndrome.
SJS Blog by Helen Milne: (SJS Foundations Canadian Support group facilitator) Click here: Make Mine Rare
Italian Stevens Johnson Syndrome Support Group
Zora's 8 year old daughter suffered from Stevens Johnson Syndrome in December of 2003
She has started a support group in Italy STEVENS-JOHNSONsindrome@yahoogroups.com
or email Lyell_baby_03@yahoo.it
[ Click here ] Stem Cell Research Foundation. The Promise of Stem Cells in Medical Research.
Nine year old Kaitlyn Langstaff lost her battle with TEN on December 17th,
2003. She will be forever missed and always in our hearts. To read more about
Kaitlyn's courageous struggle with TEN please
Click here
New web site for our friends in Sweden [ Click here ]
Award winning British Journalist Brian Deer investigates Drug sideeffects!
(Bactrim-Septra)
The SJS Foundation is a non profit organization that is dedicated to
providing the public and persons afflicted with SJS and TEN with support and
information. We are researching its causes and working with other organizations
in an effort to make lives fuller for all persons affected by these devastating
illnesses.
Disclaimer: The views and opinions of members of our support group and hyperlink sites are not necessarily those of the SJS Foundation. Please contact your Physician for medical advice.
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.
