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NRFAdmin

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NRFAdmin last won the day on September 29 2023

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  1. We should all attend, make our case heard and demand these companies fund HPPD research.
  2. It doesn’t matter what you believe. The fact of the matter is that the NRF is directly responsible for recruiting the researcher and acquiring the initial funding from the individual associated with the HPPD Foundation that gave life to this project. The PRF had NOTHING to do with it and while I welcome collaboration I have a problem with anyone taking credit for work that doesn’t belong to them. If they want to whitewash the thousands of hours the NRF put into this project, I’m afraid that’s not going to happen. We were the forerunners on this research protocol having invested many years in making it happen. Anything the PRF manages to accomplish is a credit to them, just not the MacQuarie Protocol.
  3. You know full well that the NRF was behind the MaQuarie Protocol. The PRF had no part in it.
  4. And remember, this study comes EXCLUSIVELY from the hard work and dedication by a group of HPPD patients, including Spartan who founded the Neurosensory Research Foundation. www.neurogroup.org
  5. https://cen.acs.org/pharmaceuticals/drug-discovery/Could-an-NLRP3-inhibitor-be-the-one-drug-to-conquer-common-diseases/98/i7
  6. Neurosensory Research Foundation (NRF) Survey Announcement. The NRF in conjunction with the research team at Macquarie University (MQ) is circulating an invitation to participate with the Hallucinogen Persisting Perception Disorder ICAN Protocol survey. It is vital for each and every one of you living with HPPD to register and participate. Once registered, you will receive a link to take the survey. This effort is the single greatest hope persons affected with HPPD have and reason why the MacQuarie team needs our inclusion. Thank you ——- Please click the link for survey access and protocol update: https://www.neurogroup.org/2017/01/25/peter-goadsby-needs-our-help/
  7. Anyone have any information if Rabdosia has an effect on HPPD? Once upon a time long ago I tried St. John’s Wart which exacerbated my symptoms badly and ever since I’ve been leery of taking supplements or herbal medicine. Thanks
  8. Hello Family, I wanted to share the updated donate page of the NRF. Please have a read, suggest changes and above all, after all is said and done, please share it. Thanks https://www.neurogroup.org/donate/
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