Cognitive Impairment
Вставка
- Опубліковано 7 вер 2024
- August 9, 2022
Bateman Horne Center has partnered with the University of Utah Health to conduct a Long COVID and Post-Viral Syndromes ECHO (Project ECHO). This series delivers information to healthcare professionals utilizing short didactics and case-based learning to enhance their ability to manage patients with long COVID, ME/CFS, FM, and related comorbid conditions.
Michelle Haddad, Ph.D., Director of Post-COVID Neuropsychology Clinic, Director of Inpatient Neuropsychology at Emory University School or Medicine address neuropsychological symptoms in post-COVID conditions:
- Potential mechanisms of direct neuroinvasion and indirect impacts on the brain
- The most common impairments on objective testing
- Attention, cognitive fluency, learning and memory, executive functioning
- Recommendations for assisting patients with cognitive impairment
Note to community members: We advise viewers to always speak with their medical care team prior to making any adjustments or changes to their current regimen.
Bateman Horne Center’s involvement in this program is made possible with the additional support of the Open Medicine Foundation.
I am a 3/2020 victim of covid and never fully recovered.
I have tried MANY protocols over the course of time. The one that helped me a lot is high doses (slowly working up to 3 grams) of super clean omega 3 fish oil. I use Carlson's brand,. And Bacopa, I use Himalaya brand. 1/2 of a tablet.
It seems when my brain is functioning better my debilitating fatigue is improved.
I was glad to see the Dr. at the end recommending natural products for the brain.
Thank you for your research. Please keep trying to help us!
It is very hard to keep hoping we will recover. Especially after years (for me) of no true improvement.
Also, I had the 2 Pfizer's in spring of 2021. It helped a little bit, for a little while.
Ugh... I'm am right there with you! Same time I got COVID too! This presentation was so enlightening. I'm sharing it with my doctor and husband. I appreciate you sharing what has helped you too. I hope you can find more things that help your quality of life. It's definitely a time to show much grace and patience. And find contentment in the changes and impacts to our lives. God bless.
Cognitive impairment is my worst problem from a vaccine injury from my first Pfizer vaccine.
I also developed dysautonomia/POTS, MCAS and subsequently was diagnosed with hypermoblie Ehlers-Danlos as well 😢
Thank you!
There are quite a few studies showing cerebral hypoperfusion in CFS and LC, often linked to orthostasis (i.e. it gets worse on being upright). Cerebral hypoperfusion can be measured using transcranial Doppler ultrasound, usually during a tilt table test.
Thank you very much 🙏🏽!
Could we have a transcript of her lecture?
I would love to know more about how her presentation is related to ME/CFS, can anyone help me with understanding what she and others are saying about ME/CFS in this presentation? 🙏🙏
I actually suffer neurological damage from the vaccine and am currently enrolled in an ongoing NIH study regarding neurological injury from mRNA vaccines. Very similar to long Covid.
That’s my problem as well 😢
Is it possible to have a copy of the over the counter and prescription recommendations so that I can take those to my doctors for review? Thank you. The spelling is hard to come up with when you are not in the medical field. Thank you
High dose Omega 3 fatty acids.
Phosphatidyserine.
Dextramethorphan, (Robitussin cough medicine, making sure not to get one with 8 other cold medicines included in the mixture).
@@sq5 Thank you so very much. This was great and finally someone giving me something to do to help myself. There is a lot of talk about the symptoms and that they are "gathering" information and to have something I can do is lifechanging. I was diagnosed in ninety six and have yet to get any help whatsoever. I'ts crazy what we have all been through and no answers on how to build and protect our immune systems. Oh there are people that want your money as insurance does not pay for the help we need that is for sure. I have now collected 6 autoimmune disorders - I have to wonder what is next for me.