LymeNet Flash: post covid syndrome funding

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»	LymeNet Flash » Questions and Discussion » Medical Questions » post covid syndrome funding

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Topic: post covid syndrome funding

marie
LymeNet Contributor
Member # 3980

posted

1.15 billion funding for research for covid syndrome. They also get acknowledgement of their symptoms related to the infection.

Posts: 509 | From southern new jersey | Registered: May 2003 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

While NADA for us!

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--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

I just participated in a national virtual meeting with Congressional reps, organized through the Center for Lyme Action. We asked our reps to add another 70 million to FY22 appropriations! We're at 91 million now.

This will be divvied out to research and education through the CDC, NIAID, and DoD.

I'll make a post about it in Activism so please go there to discuss!

Posts: 13116 | From San Francisco | Registered: May 2006 | IP: Logged |

Rivendell
Frequent Contributor (1K+ posts)
Member # 19922

posted

Robin, that is wonderful. Thanks so much for your effort.

I am hoping that good things will come from Covid. So many people have long haulers syndrome and will be on disability. Add that to all the people with lyme and cos on disability, with that number increasing each year. That has to inspire more research.

I am hoping that what is learned about long haulers syndrome can be used in researching lyme and visa versa.

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Herbal Treatments for Lyme and Co-Infections:
http://buhnerhealinglyme.com
http://www.tiredoflyme.com/the-cowden-protocol-for-lyme-disease.html http://www.sinomedresearch.org http://www.lymenet.org/SupportGroups/

Posts: 1358 | From Midwest | Registered: Apr 2009 | IP: Logged |

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