The APS Foundation of America, Inc Announces World APS Day, June 9th

FOR IMMEDIATE RELEASE

Date: 06/7/2010
Contact: Christina "Tina" Pohlman
Phone: 608-782-2626
Website Address: http://www.apsfa.org
Email Address: apsfa@apsfa.org

The APS Foundation of America, Inc Announces World APS Day, June 9th

The Antiphospholipid Antibody Syndrome Foundation of America, Inc. (APSFA) urges the public, as well as the medical community, to learn more about this rare disease. APS Awareness Month runs throughout June.

The APSFA is also proud to announce that June 9 is World APS Day. The APSFA would like to bring more attention & awareness to this "rare" autoimmune disease.

APS is an autoimmune disorder. Such illnesses occur when the body’s tissues are attacked by its own substances. In APS, the body recognizes certain components of blood or cell membranes as foreign substances and produces antibodies--a specialized protein the body uses to prevent infection--against them. It is the major cause of strokes in persons under 40 years old, blood clots (thrombosis) – which can lead to heart attack or stroke – vision disturbances and repeated, otherwise unexplainable miscarriages.

APS can be diagnosed with a simple blood test. It frequently is found in conjunction with lupus, another autoimmune disorder that primarily targets women.

Please join us in blogging about your experience living with Antiphospholipid Antibody Syndrome (APS) - whether you are the patient, caretaker, friend, or loved one of an APS patient. Together, we can bring awareness to this disease. We are also requesting everyone to wear burgundy on June 9th!! Please go to http://www.apsfa.org/worldapsday.htm for more information.

Knowing more about APS can make all the difference. Help us color the world burgundy on June 9th, get in the know and Get in the Flow!

Founded in 2005, the APSFA is the leading United States health agency dedicated specifically to bringing national awareness to APS. We are a volunteer-run, community-based, non-profit organization.

For more information Contact: Christina "Tina" Pohlman at Phone: 608-782-2626 Website Address: http://www.apsfa.org. Email Address: apsfa@apsfa.org

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NOTES TO EDITORS

• The key blood tests are Anticardiolipin (aCL) antibodies (IgG, IgM, and IgA), Lupus anticoagulant (LAC) – a panel of blood clotting tests that may include the dilute Russel Viper venom time (dRVVT), lupus aPTT, mixing studies, and hex phase phospholipid test, platelet neutralization procedure and Antibodies to b2-glycoprotein I (IgG, IgM, IgA).

• The conservative estimate of people at risk from Antiphospholipid Antibody Syndrome (APS) is 1% - 5% of the population.

• In pregnancy clotting of the placenta can cause miscarriage or stillbirth. Typically, women are not tested for APS until after three consecutive miscarriages.

• The recognition and treatment of APS improves the chances of preventing miscarriage from below 20% to above 80%.

• Some cases are misdiagnosed as multiple sclerosis. Some APS patients also have Lupus.

• Founded in 2005, the APS Foundation of America, Inc. is the leading United States nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Antibody Syndrome (APS), the major cause of multiple miscarriages, thrombosis, young strokes and heart attacks. We are a volunteer run, community based 501(c)3 non-profit Public Charity organization and is dedicated to fostering and facilitating joint efforts in the areas of education, support, public awareness, research and patient services. Our URL is http://www.apsfa.org

• All figures, unless otherwise stated, are from http://www.apsfa.org.

Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS, american, association, press, release

JUNE IS APS AWARENESS MONTH: GET IN THE FLOW!

FOR IMMEDIATE RELEASE

Date: 06/01/2010
Contact: Christina "Tina" Pohlman
Phone: 608-782-2626
Website Address: http://www.apsfa.org
Email Address: apsfa@apsfa.org

JUNE IS APS AWARENESS MONTH: GET IN THE FLOW!

The Antiphospholipid Antibody Syndrome (APS) Foundation of America, Inc. (APSFA) urges the public, as well as the medical community, to learn more about this rare disease. APS Awareness Month runs throughout June.

APS is an autoimmune disorder. Such illnesses occur when the body’s tissues are attacked by its own substances. In APS, the body recognizes certain components of blood or cell membranes as foreign substances and produces antibodies--a specialized protein the body uses to prevent infection--against them. It is the major cause of strokes in persons under 40 years old, blood clots (thrombosis) – which can lead to heart attack or stroke – vision disturbances and repeated, otherwise unexplainable miscarriages.

APS often is found in conjunction with lupus, another autoimmune disorder that primarily targets women.

Knowing more about APS can make all the difference. Get in the know and Get in the Flow!

Founded in 2005, the APSFA is the leading United States health agency dedicated specifically to bringing national awareness to APS. We are a volunteer-run, community-based, non-profit organization.

For more information Contact: Christina "Tina" Pohlman at Phone: 608-782-2626
Website Address: http://www.apsfa.org. Email Address: apsfa@apsfa.org

###

Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS, association, american, press, release

Spring/Summer 2010 volume of our quarterly newsletter, "Antiphospho...What??" is Available

The Spring/Summer 2010 volume of our quarterly newsletter, "Antiphospho...What??" is ready to be downloaded. You can download it at the following link:
http://www.apsfa.org/docs/APSFAVol17SprSum2010.pdf

The next volume will be coming out mid August 2010.

Please let us know if there are any topics that you'd like our Medical Advisers to cover in their articles. We try to request topics that people are emailing about or that are discussed on our the forum. So if there's anything you'd like to see, please let us know and we'll pass it along to the medical advisers.

We are still in need of patient stories (esp about Pregnancy Loss, Men and Teens or Children), recipes, poems, related book reviews, and anything else you think would be of interest for upcoming newsletters. (book reviews, poems, recipes, articles written by family members, etc.) Please submit articles to the following email address: articles@apsfa.org.

Please follow our current guidelines when submitting an article:
• Send your story/article to articles@apsfa.org
• Patient stories and most articles should be approx 500-750 words long and contain a title
• Articles should be written at a 5th-8th grade reading level
• Please try to include a picture when submitting a patient story
• Patient stories should read like an autobiography—generally from diagnosis to present time, but it doesn’t have to

Please use previous patients stories as your guideline. They can be found here: http://www.apsfa.org/newsletters.html

If you have an idea and are not sure if it would fit, please feel free to contact us through our contact page on the website, or email us using the email address below. We are open to any suggestions. Without your help we would not be able to include an APS patient's story in each of our newsletters.

We could also use articles written by medical professionals or medical students. Please contact us if you are interested.

Please remember to check our website for any changes at the following link: http://www.apsfa.org/new.htm

Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS, newsletter

Signature Tag Fundraiser

Tags, or signature tags are used primarily on forums or in the signature of emails. We are offering customizable tags representing various awareness causes including and related to APS: Lupus, FVL, Thrombophilia, Hughes Syndrome, Heart Attack, Stroke, APS/Lupus, and Infant Loss.

Tags can be ordered for a $5.00 donation to the APSFA using the form below. If you would like multiple tags we are also offering 3 for a $10.00 donation. These donations are tax deductible and you will be receiving a tax receipt via email after your purchase.

Tags will be delivered via the PayPal payment email address, so if you need them sent to another email, please indicate the email address you'd like them sent to in the extra comments section when checking out. If you need a different delivery method than email, please indicate this in the comments section and we will work something out.

Only donations via PayPal will be accepted and only by using the order form below.

Please allow a 72 hour turnaround time from order to delivery.

To order click here: http://www.apsfa.org/fundraisers/tags.htm

© APS Foundation of America, Inc

To order these tags click here: http://www.apsfa.org/fundraisers/tags.htm

If you need a specific size, let us know and we'll make one for you! These are all copyright of the APSFA. DO NOT ALTER THESE GRAPHICS. For HTML codes, please contact us. APSFA ©2005 - 2010. Our copyright Notice can be located here: http://www.apsfa.org/copyright.htm

WARNING: We will enforce our copyright!

Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS, fundraiser, signature, tags

APS Awareness, Infant Loss Awareness Ribbon & APSFA Logo Lapel Pin Sales

We have new lapel pins available! We now carry 3 different types of lapel pins: Burgundy Awareness Ribbon, APSFA Logo, and Infant Loss Awareness Ribbon. The pins are as shown above. The awareness ribbon pins measure 1 inch in size. They are die struck silver with enamel colorfill. Each pin comes with a clutch back and is individually poly bagged. The APSFA Logo pins measure 1 inch in diameter. Each pin also comes with an APS information card that measures 3 1/2 inches by 5 1/2 inches and is printed on heavy paper stock. These cards would be good to leave in a doctor's office or post on a bulletin board. A view of the card can be seen below. Awareness Ribbon Pins are $5.00 each and the APSFA Logo Lapel pins are $7.50 each.

Burgundy is also the ribbon color of the following causes: Antiphospholipid Antibody Syndrome, Brain Aneurysm, Cesarean (worn upside down), Factor V Leiden, Headaches, Hemangioma and Vascular Malformation, Hospice Care, Multiple Myeloma, Thrombophilia, William's Syndrome.

Here is a sample of the information card

Awareness Ribbon Pins are $5.00 and APSFA Lapel Pins are & $7.50 each which covers shipping, tax and a small donation to the APS Foundation of America, Inc.

If you'd like extra Information cards they are 4 for $1.00.
Payments accepted are: Paypal, Credit Cards through Paypal, Money Order, Personal Check, and Cash

To Order go to: http://www.apsfa.org/fundraiser.htm

Keywords: APSFA, APS Foundation, antiphospholipid antibody syndrome, lupus, stroke, dvt, pe, thrombosis, clot, migraine, hughes syndrome, miscarriage, america, usa, anticoagulant, heart attack, APS, fundraiser