Anyone out there on Guanfacine?
Went to Mayo Clinic to get answers. Internal MD I saw said I have long term Covid. I had a mild case in Nov '21, but a few weeks later the nightmare began. With each and every passing month, new terrible symptoms appear. As of today, I am in such agonizing pain throughout my entire body. It's a combo of stabbing-like pain and burning pain. Every morning I awaken to trembling in my chest and then the pain kicks in. I can only sleep (if at all for 3-4 hrs. Tried everything.
My immune system is attacking itself. I even developed a chalazion on lower eyelid, formed and abscess, 2 surgeries, came back again, and dry eye issues now. I also have ear pain and buzzing. I never had eye issues or anything prior and was so very healthy, like all of us.
Covid has taken the life I once knew away.
The Doc I saw prescribed Guanfacine. He said, Covid causes inflammation everywhere to include the brain and puts us in "flight or fight mode."
The BIGGEST problem I'm having is I have tried for weeks to get a hold of the Doctor I with a question on the Rx. I sent several messages through Mayo mychart, called again and again (9 times) to please have him call me and he will not and just deserted me.
I was told by his assistants he's "too busy." I can't believe a human being, especially a Doctor I drove 4.5 hrs to see and spend $$$$ doesn't have the decency to care enough and call me.
I don't know where to turn and can't stop crying in pain and mysery.
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Here in Northeast Illinois I have access to a Pain Management clinic, part of a large hospital group. (North Shore). I have had two Stellate Ganglion Nerve Blocks months apart and they have significantly reduced the overall sensations. Not a cure, but has helped a lot. A daily Protein drink, like Ensure or Boost, would also provide some nutrients. Long CIVID is an ongoing nightmare for so many.
Yes, NAC is a supplement. I get it at the office of my integrative medicine doc.
I have been taking Guanfacine (2mg, extended release, at bedtime) for over a year now, and for me it has made a *huge* difference in the cognitive issues (brain fog, lethargy, etc). I took my first dose on Christmas Eve 2022, and I woke up to the best Christmas present ever -- for the first time in more than two years I actually wanted to get out of bed and engage in the day. Prior to that I would take 70mg Vyvanse when I woke up, and then sit in bed waiting for it to kick in so I could drag myself out of bed. I have since decreased the Vyvanse to 40mg and still want to get out of bed (well, at least most mornings).
What you described about fight or flight for 24/7 I totally relate to! For months straight my heart and body was just racing and “on”. I did acupuncture, tried herbs, meditation, and nothing was helping…
I was on verapamil for the heart palpitations cause I was throwing PVC’s every 10 seconds and didn’t want beta blockers.
I found I had to rest, like a lot! I was bed and couch bound all day. Finally after 4 months it started to lessen. But then other symptoms started of extreme weakness in my body, extreme weight gain (37 pounds), aching, dizziness, brain fog, feeling like I had the flu that just wouldn’t go away.
My life as I knew it ended without warning and within a days time. One minute I was folding laundry and the next I was having never had before heart racing and palpitations that devolved into full body disability…
When I said ‘rest’ that didn’t mean sleep, that meant trying to keep my body calm. I would tell my husband I prayed for sleep. I just wanted a good night’s sleep. It didn’t come for a year.
I took Paxlovid when Covid hit me again 8 months into these symptoms. My son brought it home and I was worried. My doctor prescribed me Paxlovid at the very beginning of feeling slightly off, I took it the first day and the next day my heart palpitations were better!! Despite my coming down with Covid again. I felt better than I had all year for the first 3 days, then I got a little bit sick but not bad. But I only had 5 days of the Paxlovid and 7 days of symptoms.
I seemed to be better for 7 days then got really bad rebound. I begged my doctor to give me more paxlovid after sending him some research showing rebound was possibly due to insufficient drug exposure and the viral load hadn’t been completely cleared from the first round.
I was super sick and I think that if I would have been prescribed 10 days instead of 5, I wouldn’t have been sick again.
As well as I really wanted to try Paxlovid more. I had a glimpse that it could really help me!
I’ve stayed on Paxlovid for months now and it does really help! I take a half dose as a full dose messes with my gut.
Maybe antivirals are the answer
I would try calling again and a nurse should be able to answer your question about the RX. Or possibly a pharmacist at your local pharmacy..... pharmacists are very knowledgeable about medications. Good Luck.... I pray for you. 🙏❤
That’s amazing. Thank you for sharing your experience. It’s something I’ve considered. I have a consultation with a new-to-my-clinic PA, who’s supposedly “very passionate” about long covid and I planned to ask her about it.
If you don’t mind sharing, have you experienced any side effects and did you need to titrate your dose?
The only side effect I’ve noticed is reduced blood pressure, which is a good thing for me. I was able to lower the dose on one of my blood pressure medications. It’s possible that it has caused some dizziness, but I’ve been dizzy with long Covid for years, so I can’t say for sure if the Guanfacine made any difference to that.
For the dosage I started at 1mg/day, and after a few weeks went to 2mg.
tell me more about the stellate ganglion blocks- is it painful or dangerous? I have read good things about how it helps long covid... seriously considering it
Lots of information available online. SGNB has been used for quite a while for a variety of conditions. Low/no risk, Numbing pre injection similar to dental novacaine, otherwise no pain. 15 min outpatient procedure done in a sterile mini surgical space. Blood thinning meds need to be stopped a couple days pre procedure.
What symptoms did it help with; and will you be going back for it again?
Thank you for your feedback!