DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.message sent
email sent successfully
rareLife solutions 606 Post Road East #397 Westport, CT 06880 |
||
You are receiving this because you have an account on www.oneAMYLOIDOSISvoice.com | ||
To unsubscribe from these emails, click here |
Trusted Resources: Community Center
Online support, community stories, financial assistance
The Alnylam Act: Genetic Testing and Counseling
The Alnylam Act® program was developed to reduce barriers to genetic testing and counseling to help people make more informed decisions about their health. Genetic testing is available in the United States and Canada, and genetic counseling is only available in the United States. Please refer to the downloadable healthcare professional and patient brochures for more information. Healthcare professionals who use this program have no obligation to recommend, purchase, order, prescribe, promote, administer, use or support any Alnylam product.
Related Content
-
educationCaregiver Burnout: ResourcesIf you are already suffering from stress...
-
educationA Physician’s Guide to AL (Light Chain) AmyloidosisAmyloidosis is a disorder in which misfo...
-
educationPrognostic Impact of Immunoparesis at Diagnosis and After Treatment Onset in Patients With Light-Chain AmyloidosisObjectives: Immunoparesis (IP) is a ris...
-
educationIndependent Living When You Have FAPFinding out you have a rare genetic dise...
-
videos & visualsWhat Do All These Neurological Tests Mean? – ASG Webinar 6/7https://www.youtube.com/watch?v=IzC_yaqs...
-
videos & visualsRenal Amyloidosis by Dr. Jo Abrahamhttps://www.youtube.com/watch?v=kVAgwZPs...
-
videos & visualsProthena and the AFFIRM-AL Study: Ansgar Conrad – ASG Webinar 9/13https://www.youtube.com/watch?v=NrEjyVeJ...
send a message
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences.
More information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.