For Those Who Have Wild Type And Took The Covid Vaccines. How Many Were Diagnosed After Getting The Jabs. Pfizer 1 & 2 And Follow Up?
I track my AL amyloidosis symptoms back to Sept 2020, before I my first Covid shot of January 2021. I used my VO2Max decline as well as reviewing my bike ride journal to determine the Sept 2020 date. I was diagnosed with amyloidosis Dec. 2022, well after when I determined I has hit with amyloidosis.
(added later) I suspect that Covid did me in and triggered my AL amyloidosis. Prior to Sept 2020 I was physically fit, had no illnesses, none, for many years.
I have had all the Covid shots and boosters. No adverse symptoms at all . I was diagnosed with WILD six years ago, after double bi pass, new Aortic valve and two stents. Been taking Vyndamax since. Just turned 90 on June 3. Sex life has slowed down, but I am still "hanging in there", . No pun intended. I do a lot of crosswords and Sudoku's daily to keep my mind occupied and alert, and use a mini peddle bike for one hour every day at maximum resistance for exercise. Al
I took the Pfizer vaccines in Jan & Feb 2021 and started to have symptoms in March of 2021. I have AL
Hi Vern, Would love it. (Email address can only be seen by the question and answer creators) Al
Al, I am also impressed. Turned 90, still have a sex life, doing Sudoku s and peddling a mini peddle bike. What a set of goals for the rest of us. BTW I have been doing Killer Sudokus for several years. Have lots on my computer if you would like me to send some to you--from WSJ over the years. vern
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
Is Anyone Taking Acoramidis (Attruby) Which Was Just Approved By The FDA And Is A Competitor To Vyndamax (tafamidis)