
Bert Dohmen
410 posts

Bert Dohmen
@bertdohmen
Founder of @DohmenCapital and Creator of @HedgeFolios






Dr. Patrick Soon-Shiong just showed Chris Cuomo dramatic before-and-after brain scans of late-stage tumor patients who failed chemo, radiation, and surgery — achieving complete remission with ANKTIVA. No chemo. No radiation. Tumors shrinking dramatically in months. He says: “We got FDA approval to treat patients who failed everything… and they got complete remissions. It wasn’t a one-off anecdote.” ANKTIVA (nogapendekin alfa inbakicept) is an IL-15 superagonist that activates and proliferates natural killer cells and CD8+ T-cells while avoiding regulatory T-cell suppression, turning the immune system into a targeted cancer-killing force. Clip from this 43-second segment — a potential game-changer for late-stage cases. Is ANKTIVA the breakthrough we’ve been waiting for… or do we need larger trials to confirm? Your thoughts — drop them below. Stay informed. Stay hopeful.


I have investigated Dr. Soon-Shiong work since 2018. He is a genius. He has found how our bodies are made to kill cancer, and developed ANKTIVA, which reactivates the P53 gene to do that job. You should research it using AI. You may wish to encourage the FDA to approve it for ALL CANCERS.

Amazing, a former FDA associate commissioner @peterpitts affirmed that the mechanism of action in the approved label confirms the science of Anktiva, by the FDA itself. @DrJBhattacharya agrees with Dr. Pitts and highlights the new path just released by @DrMakaryFDA of the “Plausible Mechanism of Action” to expedite and accelerate access to the American public. Two senior thoughtful members of the panel, a former FDA senior official and the present NIH/CDC director now affirm that the plausible mechanism of action is the path to rapid access. This is what we have been presenting to the FDA for the past 6 months to desperately allow the 13,000+ requests from Americans to access Anktiva via this pathway. A groundswell of patients desperate for this to happen is growing and I am pleased that @ChrisCuomo promised that this conversation will continue… as it must.

Amazing, a former FDA associate commissioner @peterpitts affirmed that the mechanism of action in the approved label confirms the science of Anktiva, by the FDA itself. @DrJBhattacharya agrees with Dr. Pitts and highlights the new path just released by @DrMakaryFDA of the “Plausible Mechanism of Action” to expedite and accelerate access to the American public. Two senior thoughtful members of the panel, a former FDA senior official and the present NIH/CDC director now affirm that the plausible mechanism of action is the path to rapid access. This is what we have been presenting to the FDA for the past 6 months to desperately allow the 13,000+ requests from Americans to access Anktiva via this pathway. A groundswell of patients desperate for this to happen is growing and I am pleased that @ChrisCuomo promised that this conversation will continue… as it must.


🚨STUDY: COVID-19 "Vaccines" Penetrate the Human Brain and Stay For at Least 17 Months — Inciting Autoimmune ATTACK mRNA and spike protein were found inside the cerebral arteries of vaccinated hemorrhagic stroke victims. Spike protein from mRNA shots is FAR MORE dangerous than viral spike. It’s genetically engineered to stay FULL-LENGTH — making it longer-lasting, harder to break down, and more toxic.











