Post-COVID-19: The Long Haul of the Pandemic, UT Health Austin Webinar, September 27, 2021
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- čas přidán 29. 09. 2021
- UT Health Austin Post-COVID-19 Program medical director Michael Brode, MD and research director Esther Melamed, MD share their latest findings and knowledge surrounding Post-COVID-Sequele aka Long-Haulers symptoms. Individuals who experience long-term symptoms such as difficulty breathing, heart conditions, severe fatigue, following COVID may fall into this category of patients.
I think it is an autoimmune disorder, leving debri in cells. I have long covid 1.5 years. Now mild rightside weakness What has helped me is cold ease every other month. Pepto and benadryl every 3 nights. B and c vitamins. Potassium foods. I mow lawns 5 miles a day. Doing better. Good luck everyone
Same here
How about your breathing? I am 7months
@@michaeljhonfantilanan3207 how r u now brother plzz reply
Please inform your patients not to take the antibiotic Ciproflaxin or floroquinones. I am recovering very slowly from Cioro toxicity and a lot of the symptoms of long covid have similarities to Ciproflaxin poisoning. I am terrified of adding covid infection to the nightmare I am already living through. Never ever take this antibiotic. On top of brain fog, visual disturbances, arthritis, hair loss, fatigue, aches and pains, insomnia, memory impairment, and to top it off, muscle and tendon ruptures. Just a warning for everyone listening to this podcast.
Why are you recommending GET when it's a known fact thru exercise doesn't help with post viral illnesses? 18:40
Because nobody really knows anything about post viral illness and they have been ignoring it for over 40 years
What an informative video...You made my day by mentioning that most sob isn't related to fibrosis. This is my worst fear is dying with pulmonary fibrosis. Thank you Sir, Thank you sooooo much! 💖
Thanks for your info. 2 years this March. I have had so many symptoms. My chest discomfort, rib, and chest pain/tightness have been worst. However, just now getting neuralgia again in fingers, lower legs, and feet. Myalgias and just chronic pain that goes along with fatigue. Flaring worse with female cycle.
That’s my right now … the chest tightness and chest pain and it radiates to my back. It’s awful. Also symptoms flare with my cycle too. 😭 idk what to take
@@vimkosy2857 i just got labs back for positive speckled ANA. Possible covid triggered autoimmune
@@oliviaelliott4623 oh really, did your drs give you medications? I hope & pray you find relief soon 🙏🏼
@@vimkosy2857 I literally just got ANA Ifa positive and ANA speckled. Ugh. Thank you! You too. I felt like a crazy long haul patient because most my labs are fairly normal ( regular labs).
At least it's a starting point.
Thank you.
As a veteran nurse, in critical care and later a wellness cardiac and pulmonary rehab. Nurse specialist, I found this really informative in relatively short and free video on YT.
This disease is quite a nasty one. This presentation was really well done IMO. Not only for me as a health professional but also I think not too technical or complicated for most educated lay people. Well done!
Very helpful thank you 😊👍
The only common denominator between the two is the spike protein
Bingo.. the spike protein stays in the body.. we are boned
I get tremors inside like he mentioned 5 of his patient get. For me it's brought on when the fatigue sets in. If it goes on for too long my hands begin to tremble as well.
I have this too. I feel like I'm vibrating. It is hard to discribe that jumpy feeling yet the feeling of muscle fatigue at the same time. It is very distressing. I find that if I overdo physical activity, that is when my symptoms return with a vengeance.
@@Wendy-xe4gk Not great at all. I wish they would figure this all out.
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Lacey, any better?
@@shaft657 yes I am. I watched a lot of Jez Medinger RUN/DMC Videos. He advised that I rest with a vengeance and then slowly try to do things during the day in between more resting. I literally layed in bed or on a cot mattress on the floor for 6 weeks. I was able to walk to the bathroom. I started slow and prayed and things got better slowly. Now I rest a few times a day but can do a limited amount of dishes microwave myself food. I still get tired but now I do not have the terrible tremors or the 7 to 10 day relapses 3 times per month. I never never never want to be that sick again. I still am pretty mentally challenged by the end of the day. I say 'what?' A lot in the evenings becuz my brain has difficulty deciphering what people are saying. So it's bedtime when confusion sets in. :):):) thx for checking and wondering how I am doing. It takes so much time and patience I'm so happy I am on the other side of this all. Bless You
How many patients got better with long haul symptoms after PAXLOVID!?
Any one suffering post Covid with lower back pain?
Yes, I do. Had it when I had Covid and it's come back again with other joint pain, very frustrating. Wishing you the very best. I'm certain the body can figure it all out in time.
Yes & no. My lower back pain is ongoing for 14 months post second Pfizer jab. Very difficult. Worried it may be symptom of other diseases such as ovarian cancer. Am thinking to get an xray to be sure spine's ok. Then engage in a few acupuncture apts targeting the lower back.
@@ladybug5859 sorry to hear that. Sending love and prayers. 👍🙏
looks like you have a big update on the vaccines to do
I have severe post covid rash/chicken pox- whatever u want to call it- new pox every day - into week 3 of this now and this is all after 2 weeks of covid..............
Did people have the vacine first before symptoms began mine came 3 days after 2nd vac
Covid destroyed my GI tract. Chest pain severe still 3 years later. Now I have small fiber nerve pain that is debilitating. Especially around my lower rib cage. Feels like being tasered and a heart attack 24 seven. Tests don't show anything to explain it. I don't have a life anymore. I'm looking for a specialist in long covid. Or to participate in a study. Support group.. anything! Also have had total insomnia the whole 3 years. Getting VERY tired of being dismissed or told it's stress or all in my head! So glad to see this. I'm in Austin. Do you know who's out there to help, anyone?
i’m in the same 3-year boat, except that my chest pain is gone this year. i’m sorry that you’re still so sick. have you tried any of the “covid centers of excellence” like mt sinai in nyc to see if they’ll see you by phone or computer? i think i remember that the one in chicago will see you that way, instead of traveling.
Autonomic dysfunction will cure in post viral illness?
So almost one year later and we don't seem know much more.
Just saying you BELIEVE us is everything. My healthcare in NW Michigan in 2021 was terrible. Not being believed really upset me. 18 months now.
I think the drs just didn’t know any better.
CHRONIC
by Steven Phillips, M.D.
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Can u send me your PASC treatment recommendations?
Have always depressed, since birth. I've been ill for 2 years after having a bad bout of covid. Two weeks ago I started feeling better. Ive never been better
Among few other symptoms of long covid, 2 and half years after having covid and 1 year and some after 2nd Phizer dose (which landed me in hospital for 10 days for pericarditis), I still get these vibration-like shakes throughout the body, besides having many symptoms of long covid. Whole life is sort of upside down. And now Boston University is working on new "improved" virus, Omicron-S, which is 80 times more deadly dan original virus.
it says there are 92 comments but I only counted 27🤔🤔
Yeah. I see that happening a lot. Or you can't read the "more" on longer comments.
14.56 the body really is shaking. :(
Thanks Wuhan!
It just really is so bad