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evgenimat
@evgenimat

Posts: 1
Joined: Jan 08, 2018

Two Months After POEM Surgery for Achalasia

Posted by @evgenimat, Mon, Jan 8 11:07am

Hi everyone,
I’ve had achalasia that progressively got worse over the course of three years, to the point where I almost couldn’t eat without throwing up, and drank at least a liter of water with every meal. I just had a POEM surgery done in November (2017) with Dr. Robert Bechara in Kingston, Ontario. I wanted share my experience because, like many people here, before my surgery I scoured the web for hours trying to get an idea of what I should expect. I ended up being very anxious about the surgery, afraid that it wouldn’t work or even make things worse. I now know I fell victim to confirmation bias, since people are much more likely to post a bad experience rather than a good one, and I want to dilute that a bit.
Like many, I was first diagnosed with GERD and took Proton Pump Inhibitors, which obviously didn’t work. After a barium swallow, endoscopy, and mamotomy (ugh), I was correctly diagnosed with Type I achalasia and was lucky enough to be scheduled for POEM only three months later. Dr. Bechara and his staff were incredibly friendly, communicative, and accommodating to the fact that I lived out of province. Dr. Bechara studied in Japan, where the procedure was developed, and had a success rate of 100% from 100 patients that he’d done the operation on. Contrasting to how nervous I was, he seemed to almost be bored. In fact, the day I had my operation, he had another person getting it too. So, he’s a total expert. Do ask your doctor how many operations they’d done and if they had any complications, if nothing else it’ll put your mind at ease.
Three days before the operation I was on a fully liquid diet, which isn’t bad but really drains your energy. All I wanted to do was lay in bed and watch TV, so don’t plan any marathons. The morning of the surgery I was put on IV and right before the surgery I was knocked out and put on anaesthetic. All I remember is the count down, and the next thing I knew I was coming to in the post-op room. At first the anaesthetic was still working so I felt sleepy but great. As it wore off though, I started feeling a pain in my chest. Getting up was out of the question for at least a few hours, but they gave me a fantastic pink numbing liquid (Lidodan 2%) which worked wonders. I was pretty much bedridden for the next three days, and had almost no energy for anything. So take that week off work is my advice.
This pain remained for about three weeks, and, I’ll be honest, it really sucked. At first it was a constant dull pain that inhibited my breadth of movement and would only be subdued by the pink stuff. After about a week the pain became acute, which was worse. I would feel almost totally fine, and then this sharp stab would suddenly come on and I had to lie down wherever I was; always have your pink stuff (or Tylenol) on hand. I thought these was the spasms some people wrote about in blogs and was afraid it wouldn’t go ever away. I definitely had thoughts that this wasn’t worth it, and I should’ve just lived with the swallowing issues rather than inhibiting spasms. BUT, the pink liquid was awesome and it would calm the pain in about 30 minutes, and it did go away after three weeks. It became less and less frequent, and now totally gone. The pain is not that surprising really, they put a 17cm incision inside your body – its gonna hurt. After a week after the surgery I was able to work just fine.
Right now, two months post-surgery, I feel so incredibly grateful that I had the operation done. I can eat all my favourite food not only without throwing up, but with consuming only a small amount of water (often not even necessary). I’ve started feeling thirsty again, can eat until I’m full, and have finally started regaining the weight I’d lost. If you have a chance to do this operation, do it. And I would highly recommend Dr. Bechara if you have the opportunity. Good luck, and don’t give up hope!

REPLY

Hello @evgenimat and welcome to Mayo Connect!

We appreciate your sharing your story of achalasia and about your successful surgery. We are so glad that you have experienced so much help after 2 months post surgery.

I’m sure your experience will encourage others who are considering surgery as treatment for achalasia. We all learn from each other at Mayo Connect and we are glad that you have added to this learning.

How much follow-up will you have now?

Teresa

@evgenimat ,
Thank you for sharing your experience. So far ablation is working for me, but I know down the road it will not. It is nice to know of other’s experiences. You are correct.. one finds more negative than positive when researching. It is nice to read of a positive outcome. I pray it continues.

Zaroga

Thank you for posting your experience. I am having this procedure done this month and I can not find very much info relating to what to expect post op.

I am 10 days poet op the POEM procedure. Your note has been the most helpful reference I have been able to find. I am feeling much stronger now that I am on puréed food but the pain is sometimes debilitating. Did you find sleeping difficult some nights at this stage? By the way, I have not been offered the ‘pink liquid’ so the pain has been a real challenge. Thanks for your note, it is balanced and a real public service. JP

@pjstatham

Thank you for posting your experience. I am having this procedure done this month and I can not find very much info relating to what to expect post op.

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@pjstatham– just reading your post and wondering how your procedure went?

@jphilp

I am 10 days poet op the POEM procedure. Your note has been the most helpful reference I have been able to find. I am feeling much stronger now that I am on puréed food but the pain is sometimes debilitating. Did you find sleeping difficult some nights at this stage? By the way, I have not been offered the ‘pink liquid’ so the pain has been a real challenge. Thanks for your note, it is balanced and a real public service. JP

Jump to this post

Hello @jphilp. Thank you for posting. Welcome to Mayo Clinic Connect!

Do you have to sleep sitting up? What do you find most difficult?

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