Quick Links
About MyAmyloidosisTeam
Powered By
Does Anyone Have A Suggestion For The Best Place To Go For Diagnosis Of Rare Diseases. I Am Willing To Travel.
I have been going to Kaiser here in WA for 7 years. I am getting sicker by the day. They think well inside the box. I can't do this any longer. I am 75 and have no life, no meds, and no hope at this point. Please help.
I would go to Mayo clinic in MN.
jim4
HMO's are profitable oriented. Not where you should be at Kaiser.
I am at the university of TN hospital.
I think Cleveland Clinic is probably good.
How about Stanford in CA heard they have a great amyloidosis center? Prayers to you πππ
I go to Vanderbilt in Nashville. I see Dr. Muhamed Baljevic heβs the best!!! (Phone number can only be seen by the question and answer creators)
Will Acoramidis Replace Tafamidis If Approved In The US? Will We Have A Choice?
Anyone See Any Updated Life Expectancy With Tafamidis? Surely Someone Has Updated This Somewhere Since It Has Been In Use For Years Now
Are There Independent Labs That I Can Go To In Order To Have Complete Proactive Testing Done?
Sign up for free!
Continue with Facebook
Sign up with your email
