Everyone with two shares short Posting. It's just too bad we have to put up with this crapola on Yahoo without better BLOCKING ignore user feature.
l that's news after 4 years. Suddenly you "jcordaly" discover this hidden fact NOW and are sharing this explosive tid-bit. Better call the FDA, FCC, BBC and FBI they all seemed to have over looked this drama.
24 weeks showed ADL improvements without Dystrophin showing that much on some kids . However, the parents and kids know it's working. By 48 weeks both ^ADL and ^labs, a bit low if advance with the less muscle to treat. Early reports suggest kids having Positive changes to ALDs on the extended study.
First, it's in the tissue. The tissue is damaged includes major scar tissue and fat. A Small amount of tissue still works if repaired. You will see new protein in whatever undamaged tissue you have. The first kids were so close to failure because they had only a limited available muscle tissue. So low levels would be expected. Earlier kids may have more dystrophin made only because they have more remaining Muscle.
My example, if you had a 1% battery to save your life would you use it? Or be afraid of the call being dropped? These late stage kids have that 1%, and enough to keep them going. Earlier kids would have a bigger muscle battery that could charge let's say to 9%. A winner long term.
Thier are many Monuments overseas, Germany, France Belgium, North Africa. We are coming up on 100 years from WWI. I hope some of you can make it to anyone of those Cemeteries and Battlefields. I would suggest Verdun FR, Bastone or D-day areas. Verdun, walk into an open square miles field and survive. Our soldiers did the improbable with daring and grit. 28,000 in battle and 50,000 or so from flu.
MD Farkas must have a Jerry Lewis clown phobia the way he keeps destroying hope of the DMD community. With no background or expertise in DMD he has single handedly delayed treatment for over 4 years. Even after experts explained and pleaded with a FDA panel in 2014 he still failed to grasp how DMD works.
If rare diseases can't count on the US FDA for fair science reviews, instead factless invented arguments because of poor leadership or unqualified FDA reviews, then the rare diseases area is wasting time and money in the USA. These Companies spent $Billions, risked children's lives for a cure and the FDA can't take the time and effort for qualified reviewer?
With this board being polluted by trolls and no way to block "Users" 100% so they don't show in any headlines. Twitter may be the better location to communicate. Block means Block on Twitter. Clown trolls like we have here are a waste of my good time.
It might be why Schwab was asking for permission to borrow my shares. Where as before they just created shares to short.
It will allow Suits in Friendly anti-naked shortsale States. RICO and Fraud counts in State courts not just Federal Courts.
Enroll in SLFP, and you can receive monthly income for lending securities to Schwab that are in high demand by other investors. So...My only high demand stock is SRPT. It does mention shares being sold short could hurt my share price.
I did not look into the particulars. How much and so on. If it paid enough I'd buy shares just to lend. Pick every short target.
What do you suggest we do for those kids? Label them as the "the Kids Farkas killed". Let them die? Oh boy the FDA is going to just love the feedback they get for those moms.