← Return to No wonder there is so little being done about Neuropathy!

Discussion

No wonder there is so little being done about Neuropathy!

Neuropathy | Last Active: Jul 14, 2021 | Replies (78)

Comment receiving replies
@catharbert

Please see the Foundation for Peripheral Neuropathy newsletter for information on Congressional action to fund research::
https://www.foundationforpn.org/2020/11/06/advocating-for-peripheral-neuropathy-research-funding/?blm_aid=1754340353
Update on the 2021 Appropriations Bill

On November 10, 2020, the Senate Committee on Appropriations released their version of the fiscal year 2021 Defense Appropriations Act. We are excited to report that this legislation includes “peripheral neuropathy” among the conditions eligible for research under the Peer-Reviewed Medical Research Program (PRMRP).

Jump to this post


Replies to "Please see the Foundation for Peripheral Neuropathy newsletter for information on Congressional action to fund research::..."

Just how much research does the Foundation need? The world wide research has certainly proved that the brain is plastic, and and that the practice of Neuroplasticity can provide relief in many areas including a cure. I have , after 3 months, experienced great progress, as have many world wide.I looked at the Foundation's Website and was amazed that there was not even a mention of neuroplasticity. I even sent a message to the foundation protesting thier6 lack of leadership or encouragement to PN sufferers. I feel there are two reasons for this lack of interest and leadership. One is that the the Foundation is choked by beautocracy, right from the top, or pressure from other financial interests.

Thank you so much! 😊