Shaggy
Member
I take one a day.. should I not take one every day? It's not like a doc told me to take it, things just work better when I take it...
I just alternate every other to stretch the bottle cause of the cost and that still works for me.
I take one a day.. should I not take one every day? It's not like a doc told me to take it, things just work better when I take it...
Oh no, hope you continue to improve! Which shot did you get?
Sorry to hear that. I’m sure it frustrates you now with people who are anti-vaxx and think covid is much to do about nothing. If everyone only had your perspective....
I hope you improve quickly. You’re very lucky you left the hospital alive, it’s likely that first shot helped at least a little bit.
Prayers going up for ya. I never reached the point of vaccine and didn’t require a hospitalization. I got regeneron on day 10 of symptoms, all accounts I’d say it was a mild case, but here I am 7 weeks later still fighting the effects. O2 be great but at times it hurts or seems impossible to take a really deep breath. Get headaches, upper body weakness and still not much of an appetite. I think I also have what I’ve heard called covidsomnia, I can go to bed and end up wide awake a few hours later unable to go back to sleep even though I’m exhausted. I think what might have made my symptoms worse is the fact that when I got Covid I was probably pushing 335 lbs and have high -- and vitamin d3 deficiency, essentially enough to make a really bad outcome. I lost easy 25 lbs during the actual sickness and I have continued to lose weight due to walking 2 hrs a day and watching my diet. I’m now down to about 295, a 40 pound drop in about a month in a half. I had a ct done today of my lungs for my pulmonologist to review because last month I had a ct of pelvic area for kidney stones and it just caught the bottom of my lungs and it showed some scattered ground glass opacities in my left lower lobe. I’m praying this has cleared up and the rest of my lungs are ok. I use a spirometer just about every hr to try and strengthen them and pulmonologist ordered me a nebulizer that I use Ipratropium and albuterol on my really bad days. Sorry for the long post, just wanted to share what I’m experiencing and again my prayers are with you. I told my wife when I hear someone say this is just the flu, I want to smack them into next week. Yea majority do recover quick and have no lasting issues, but seems like the ones fighting issues are on their own
I just had an upper endoscopy done due to sustained weight loss since I got covid. Turned out I have really bad gastritis. My entire stomach lining is bright red. Now I’m on a special diet and the only “treatment” is avoiding food/drink that makes things worse. Funny thing is I’m a pretty healthy eater, I also don’t smoke or drink. Don’t drink soda or carbonated beverages or coffee. I don’t even drink fruit juices— only water. So to say it’s odd is an understatement. People they see with gastritis usually have a very obvious cause. I’m hopeful it just heals in time.
There’s just a lot we don’t understand about covid-19’s lasting impact and I just hope people realize it’s not just about the headache or cough, and it’s not just the flu..
So I got C. diff apparently . This is the second time ! I’m a -------- student I can’t do 3 different horrible flare ups 2 rounds of c. Diff and COVID . My poor poor poor grades !Just got report back on my lung ct from yesterday. Nearly all the scattered ground glass opacities in my left lower lobe is gone. Says minimal amounts are left!! Rest of lungs are clear. Everything that showed up on ct looked great. Nothing showed as enlarged including my heart. Seriously think my issue is gastro/gas now. Such a relief to see that good of a report. Hopefully it will calm some of my anxiety over this junk.
So I got C. diff apparently . This is the second time ! I’m a -------- student I can’t do 3 different horrible flare ups 2 rounds of c. Diff and COVID . My poor poor poor grades !
First time around I was on vancomycin . About to pick up my antibiotics now so we will see what it is this time .What did they put you on? Vancomycin or flagyl? You could be a candidate for a poop transplant
First time around I was on vancomycin . About to pick up my antibiotics now so we will see what it is this time .
It’s weird because I don’t feel as bad as I did the first time I got C diff. First time was hell times 1000000000000 , this time around it’s hell time’s 1000. Maybe my body can fight it better now I don’t know ?I did 4 rounds of vanco and 1 of flagyl before I cleared up. Best of luck man.
CDC says the B.1.1.7 variant is now the most common lineage in the US.
Definitely interested in this. Larry, was you pretty weak for awhile after your recovery? I can walk on treadmill at 2.4 mph for 45 minutes and be fine. Today my wife and I put together a gas grill and I thought I was going to die. Absolutely no upper body strength and just no energyI'm assuming I had the original strain when I had COVID back in January. Does @Jon or anyone else know if I'd likely be protected from the B.1.1.7 variant for awhile due to antibodies from the original strain? Or would that just protect me from the original strain?