After visiting with hundreds of patients with Post COVID Syndrome (PCS), we have learned a lot about the early steps in recovery. It turns out, you don’t need us doctors to get your recovery started! Here are my tips on how to beat PCS on your own.
- Allow yourself time to recover
One thing we have seen repeatedly is that patients push themselves too hard while trying to recover. It makes sense. Everyone is so eager to “get back to normal life” after their infection and isolation. It is tempting to just grit your teeth and bounce back to your usual lifestyle. But when patients do this, they experience a flare of their fatigue, shortness of breath, and muscle aches that can last for hours to days at a time. During this time, patients are forced to rest and feel they become even weaker. Then they try to resume life again, experience setbacks, thus repeating the cycle until they are very demoralized and deconditioned.
So, doctor’s orders: Give yourself time to recover. The fastest way to recovery is to take things slow and easy at first, and then trying to gradually increase your activities. And I’m not talking just about traditional rehab activities. Your regular daily chores count as part of your rehabilitation. For example, if you can do one load of laundry a day without worsening of your symptoms, wait until next week to try two loads. Same for mental activity. Taking a break does not mean its time to write that book you’ve been meaning to get to.
Remember that you are in a recovery from a serious infection. Because of your symptoms, you won’t be able to do everything you normally would do during each day. And that is okay. Instead of trying to do everything and failing, focus on things that are a priority. This pacing is the key to getting back to baseline more quickly overall.
- Hydrate and eat healthy
During the acute infection, many patients aren’t very hungry. This can be made worse if there are problems with taste and smell. Some patients get used to this and forget the importance of good nutrition. Focus on getting in a good amount of hydration in during the day (2.7 – 3.7L) per day. As for diet, we haven’t found that any diet is best. Only that fad diets and extreme diets will make things worse, especially for your bank account. What I recommend is a balanced, Mediterranean diet. Of course, try to resist processed and high fat foods.
- Focus on resistance activity
When patients try to do some physical activity after COVID-19, they often try activities that get the heart rate up. Like walking and cycling. This makes sense; people want to get outside or go somewhere after being cooped up for a while. However, we find that cardiovascular exercise is the most difficult type of activity for patients with PCS. So instead, start with more resistance type activities, such as band work, light free weights, yoga, or Pilates. Once this goes well, then you can throw in some light cardio.
- Optimize your sleep
It is very common for patients to have problems with their sleep after a COVID infection. This is worse with PCS as many patients will end up taking naps. This can throw the sleep schedule making it hard to get the body back on the right schedule. It is important to get the best sleep possible.
Start of by making sure your sleep area is ideal. You should have some airflow and most people will sleep better with the room slightly cooler than during the day, around 68-70 degrees. You also want to minimize electronic distractions; using your phone in bed is a great way to keep your brain stimulated just enough to keep you awake. Of course, try to avoid caffeine after lunch and exercise within two hours of sleep. Finally, try to work towards a normal day time schedule by waking up at a certain time, getting your meals in, and having a routine bedtime.
- Olfactory retraining
Not being able to taste and smell normally totally stinks. About a third of patients have prolonged troubles with taste and smell after the acute COVID infection. Fortunately, most patients will get better within 6 months, and even more within 12 months. If you want to speed things up though, I recommend olfactory retraining. A great website to help you is abscent.org https://abscent.org/.
I know that it is hard to find care for PCS. Fortunately, the ideal recovery starts with you in your home.
Connect with other people like you and share your recovery tips and successes in the Post-COVID Recovery & COVID-19 support group.
Yes and I loved it.
Were you able to find affordable lodging while there?
Check with you insurance company they sometimes have a 50 day rate There is a courtyard on campus and there short stay places and vrbos
I’ve been walking with a few people in my neighborhood. Some have had Covid, but most with the same lingering tired feeling that I have. We all have experienced the same feeling whether we walk or not.
PCP don’t offer much assistance.
So we’ll continue walking and support each other.
My mistake was to try to prove to myself that I was still “normal.” In hindsight, it was reckless, and continuing to work just led to crappy work and probably limiting my recovery. I’m taking time off at the end of the year. With the weekend, eleven days off. I only took a couple sick days off and partial days for Covid medical stuff. Brain fog is bad this week. I think I’m still overdoing.
Acupuncture was able to minimize the horribleness of the periodic fatigue when it came on. It was like a light switch, with immediate improvement (considering I was falling asleep during the assessment just before treatment, it was pretty night and day). It has not reduced the frequency of the periods of fatigue (where I am not able to work or tend to my children between 7am-8:30pm; it could be going to sleep at 1pm and not waking up until the next day or sleeping at 6pm), which concerns me, but I don’t feel as deeply bone tired as before when the fatigue occurs.
I see an acupuncturist 2 or 3 times a week, and it has definitely helped with fatigue post covid. Probably also helping the whole body to restore to health in many different ways.
An experienced acupuncturist though...very much better.
I’m new— I got Covid 3/2020. Severe illness. But, I thought I was doing better slowly until 12/21. Since then it’s been up and down. I am in a long haul clinic, but when I got an illness had to stop attending. It’s flared up in full. Does this ever stop, do we know?
Will another infection cause flares?
i got covid Dec of 2019, i'm still dealing with this long hauler thing. there have been a few times i thought i was getting better but i was wrong, it's like one step forward then ten steps back...the phlegm i get is still bad, brain fog still bad and the weight thing..every time i can lose a pound, two to three come back,my body really fights me on losing....plus a whole mess of other symptoms, this virus has really messed us up, we just can't give in to it so keep fighting!
It doesn't help that the doctors don't have a clue, don't care or are in total denial. I've been subjected to some of the most all-encompassing GI pain, Joint pain (Either joint inflammation or nerve) that I've ever had including sciatica, gout and abscessed tooth - yet complete denial from the medical staff as though it's all in my head. Pulmonary distress, exhausted, shortness of breath, continual phlegm and irritated throat - tounge and the worst headache I've ever had. To my medical community - it's all in my head.
You can't tell me the medical community doesn't know what is happening to us, nor do I believe they have no protocol to treat the symptoms nor how to investigate the potential damage to our organs. All I know is on May 7, 2022 I caught Covid and for the first time in my life I felt like I was truly dying and for the last 10 months my doctors have been totally useless.
I don't expect my primary care physician to cure covid, or for that matter understand it. All I'm asking is he treat my pain and do enough investigative work to assure me my lungs aren't being scarred or my heart isn't one beat away from a stroke ... Just something to releave the pain and fear. Not too much to ask in my opinion.