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
Amyloidosis Support Groups Inc. – Facebook
Patients, caregivers and loved ones with AL amyloidosis – If you do not answer the questions you will not be allowed to join.
We have other groups on Facebook for hATTR Amyloidosis FAP-TTR- Hereditary, Wild Type Wild Type- ATTRwt -wtATTR,, Amyloidosis Gelsolin Hereditary, Amyloidosis-Localized Airway, Amyloidosis- AA- Secondary amyloidosis, Amyloidosis-CAA- Cerebral Amyloid Angiopathy, Amyloidosis Widow/ers Support Group, Amyloidosis Orphans, Amyloidosis Took My Sibling, Amyloidosis Took My Child
If you wish to join this group you must have the disease, have a loved one with it or caregive someone with the disease.
Related Content
-
people & placesDeutsche Gesellschaft für Amyloid-Krankheiten e.V.Die Gesellschaft wurde 1993 in Garmi...
-
videos & visualsPrem Soman on Tc-99m PYP Scan to Diagnose ATTR Cardiac Amyloidosishttps://www.youtube.com/watch?v=EZCnGFiq...
-
news & meetingsLight the Night for Amyloidosis — Amyloidosis Foundation“Light the Night for Amyloidosis” is...
-
news & meetingsRare Disease DayRare Disease Day takes place on the last...
-
news & meetingsRare Disease Day Symposium at the Quinnipiac Frank H. Netter MD School of MedicineThe Rare Disease Day Symposium at the Qu...
-
people & placesStephen E. Fink Memorial FundStephen E. Fink was a son, a brother, an...
-
people & placesATTR Amyloidosis Patients AssociationThe UK ATTR Amyloidosis Patients’ Asso...
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.