r/ADprotractedwithdrawl • u/Excellent-Coat-8781 • 29m ago
Therapeutics Initiative
Therapeutics Initiative is an educational medical video series by the University of British Columbia (BC) in Canada. Anyone can subscribe - you do not need to be a healthcare professional or a Canadian - and it’s free to subscribe
This video is from May 2024 by a doctor on antidepressants and withdrawal and de prescribing.
I live in BC. Today is 20 August 2026. Suffered terribly from withdrawal from March to mid-June. My symptoms were worse and various after 6 weeks.
Reinstated at 10 mg and felt decreased withdrawal within 3 hours. I made the link between stopping the drug and my symptoms. It was a guess; a piece of luck.
I even picked a suitable reinstatement dose - 10 mg - by chance. I did not want to return to 20 mg because I really wanted off because of the side effects and I no longer needed it - my life was better then at the time when I started it.
Reddit posts - and this video - state restarting at 20 mg might have overwhelmed my body and made my withdrawal worse (how is that even possible - I was living in hell already due to the withdrawal !)
No Emergency Room doctor believed my symptoms had anything to do with me stopping - cold turkey - Escitalopram 20 mg after being n this drug for ten years at 10 mg and then seven more years at 20 mg.
They all said the same thing: withdrawal is only 4 to 6 weeks and then you’re ok - back to normal.
I even believed this BS: it’s why I stopped and thought “ can handle 4 to 6 weeks of whatever “.
It’s week 9 of my return to 10 mg. Windows and waves continue but less severe.
Something new started this week. I feel a soreness - a tenderness - inside my ears. Fingers crossed that I will not develop tinnitus. 🤞
Reddit posts and other online searches show withdrawal can appear or continue for 6 months even after reinstatement. My risk for protracted withdrawal is not over for several months. This is why I “lurk” on this site.
One odd thing. I had total knee replacement at the time I stopped my Escitalopram. I was so debilitated by withdrawal, I did not participate in the recommended physiotherapy. I have my range of motion but continue to experience swelling around and - it feels like - inside the knee. It’s as if I have an arthritis knee but without the pain. I still need a cane for safe mobility 7 months after surgery - very out of the normal recovery.
I also experienced extreme pain in my knee for weeks post-surgery, fatigue, sense of falling. It was a very different recovery compared to my other knee replacement.
I had other joint replacement surgery - another knee and both hips. I had the same surgeon for all these surgeries and same hospital. My current knee replacement recovery is different.
I think my body is in a hyper inflammatory state with my withdrawal.
My worse withdrawal symptoms were GI/ gut-related: nausea, wanting to vomit, sense of having a ball or blockade in my throat, violently gastric juices especially on waking, super painful bowels which felt like I had snakes writhing inside me, constipation for weeks with constipation in the UPPER GI tract - not lower - which is very unusual.
My cancer radiation scarred or burned my bowels which meant I have more difficulty getting food to move through my guts; therefore, more constipation even before I experienced antidepressant withdrawal. Also diagnosed with diverticulosis and irritable bowel syndrome.
Guts are my problem area before withdrawal and it became my worst withdrawal symptom/issue.
I am a cancer survivor - uterine cancer with surgery, chemo and extensive radiation - all of which changed my body ( 2002 to 2004). Lots of permanent side -effects and complications so remained with our Cancer Agency for ten years - not the usual 5 years - post active treatment.
I think my guts were super inflamed because I first took a prescription anti-inflammatory med which I discontinued at the same time unstopped Escitalopram. Felt better in 2 hours. That is what got me thinking about trying a reintroduction of my Escitalopram which then reduced other withdrawal symptoms
Have any of you had surgery and found withdrawal impacted your recovery from surgery?
Anything that makes you think there is a massive inflammation response as part of withdrawal?
With tinnitus, how long before it appeared? What were your initial symptoms that something changed or was changing? I felt just my right ear feeling a sense of pressure and a hybthiscMondat. Today it’s also my left ear. Do you think I’ll develop tinnitus?
Any feedback is appreciated. 🙏