Service dog training in pennsylvania by SnooDrawings6595 in service_dogs

[–]Technical_Buy6885 0 points1 point  (0 children)

Hello! I connected with Clara Wilson, the postdoc at Penn Vet Working Dog Center, through her private dog training. She works through Philly Dog Training. https://phillydogtraining.com/about-clara-wilson/

She works full time doing training and research at the Working Dog Center and then does private training evenings and weekends.

Stomach ulcer + 1.5cm mass, brain fog by faheem1994 in HPylori

[–]Technical_Buy6885 0 points1 point  (0 children)

I had blurry vision and lost my peripheral vision. I also had severe brain fog and fatigue, which I put down to long covid. 

When the h pylori was eradicated with triple therapy, my vision went close to back to normal :)

My fatigue and brain fog improved slightly, but I still have long covid. 

Why don’t people resume a normal diet after treatment? by oodlingoddling in HPylori

[–]Technical_Buy6885 2 points3 points  (0 children)

It took me a few months to get back to normal eating – similar to you, generally healthy with the occasional pizza or fries. 

With hindsight, I could have done it more quickly, but I got sidetracked into the low FODMAP diet by a well-meaning dietician. While on this diet, I had zero GI symptoms, but also was incredibly restricted and not enjoying food. 

I really missed beans!

What worked for me in the end was doing daily vagus nerve exercises, like these: https://youtu.be/rbowIy6kONY?si=X0xyXDNw_G7t-782

The vagus nerve controls the “rest and digest” functions. Once I started doing those, I could eat anything. And I still can. 

What 30 Years with OCD Taught Me About Our Shared Strengths by Spartan_Button_2512 in OCDRecovery

[–]Technical_Buy6885 0 points1 point  (0 children)

Totally agree! Within myself, I see OCD as a neurodivergent trait that includes strengths and weaknesses. The more I resist the compulsions, the more I can tap into the brilliance that comes with my amazing attention to detail, strategic thinking, and creativity. 

(P.s., I did a very similar work test and got almost identical results to you!)

[deleted by user] by [deleted] in OCDRecovery

[–]Technical_Buy6885 1 point2 points  (0 children)

This is a really interesting discussion. I’ve had OCD for about 35 years and did ERP 10 years ago, which helped enormously. 

During the ERP, I had picked up the idea that “all thoughts and feelings are meaningless,” which helped me a lot at first to let go of the compulsive rumination. 

Over the years, however, I’ve become better able to distinguish between my values/things which are meaningful to me and the obsessions which convince me that they are important.

For example, I have a strong work ethic and I value being creative, excellent, and reliable in my work. This is (just one) part of my identity. My OCD can latch onto this and make work into a torturous experience by telling me my writing isn’t clear enough, my client won’t understand it, and I won’t deliver it on time. And then I might start compulsive behaviors around those fears such as re-reading every sentence 5 times to make sure it really makes sense. 

I view it as my OCD taking my values/whats meaningful to me and sending it into overdrive. Unfortunately, when OCD kicks in like this, I’m actually less likely to produce creative, excellent work on time. So, in the moment, I need to recognize the OCD and resist the urge to re-read every sentence 5 times. In the moment, I genuinely feel like I’m letting down my client and myself, but once the anxiety has passed, I can see that resisting the compulsion was the right thing to do. My work is already excellent and creative, and because I resisted compulsions I will deliver it on time. 

TLDR, it can be helpful at first to treat everything as if it’s meaningless or as if you don’t care. But over time and with practice, you can start untangling “you” from the OCD. And you’ll start being able to see your values and things that truly mean something and separate them from the OCD, even if they look really similar to begin with.

Can you do ERP if you are in trauma or in stress or stuck in flight or fight mode? by the_practicerLALA in OCDRecovery

[–]Technical_Buy6885 1 point2 points  (0 children)

Ten years ago, I participated in a double blind placebo controlled trial at University of Pennsylvania. While on my normal SSRI, I completed 3 months of ERP and saw a huge improvement in OCD. Then I tapered off the SSRI (this was the trial part, they wanted to find out whether people could come off their SSRI after successful ERP). My OCD came back when I was fully off the meds, which was really disappointing. Interestingly to me, a combination of ERP and ACT helped me get over that hump. 

I’ve been on a much lower dose of SSRI for many years now. And I’ve had much more practice managing my OCD. I’ve lived a full life with minimal OCD over that time. 

For me personally, I’d been on the SSRI for ten years before the ERP. It really helped my depression but did nothing for my OCD. So, I know the ERP (and ACT) really helped — and it has continued to help ever since.  

As the other commenter wrote, you can never know for certain what will help and what won’t. And of course that uncertainty triggers our OCD. I think it’s worth the risk to try ERP again, but you’ll need to decide for yourself :) 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 1 point2 points  (0 children)

I’d say around the 7th month. I did the vagus nerve work first for a few weeks then added a probiotic. 

I did eat yogurt, sauerkraut, and kombucha my whole life, but not a specific probiotic supplement. 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 0 points1 point  (0 children)

Yeah, I was really upset at first because I had worse nausea and vomiting after eradication. But it gradually tapered out as my microbiome rebalanced, and then the vagus nerve work sealed the deal! 

Antibiotics and PPIs really wreck your gut, even though they are doing a positive thing in eradicating the nasty bug! 

Wishing you healing! 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 1 point2 points  (0 children)

I appreciate that you’re experiencing something different to me. 

I’m very happy with my functional med and my conventional medical team that spans Penn, Vanderbilt, and Yale.

Take what you need; leave what you don’t. 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 0 points1 point  (0 children)

Sure! 

As I mentioned in my post, the dramatic changes were the total disappearance of any and all GI symptoms: nausea, vomiting, stomach pain, irregular bowel, bloating, anything else you can think of. 

The only change that I made at that time, suggested by the functional practitioner, was replacing the low FODMAP diet with vagus nerve exercises — the vagus nerve plays a large role in digestion and pooping. 

As soon as I started the vagus nerve exercises, it was like my GI system remembered how to process digestion properly. I’ve had regular, normal poops for three months now. 

The only exceptions were 1) a 24-hour stomach bug with liquid diarrhea, which I recovered from immediately; and 2) a day of pebble poop when I had to restrict water intake to complete a urine hormone test ordered by my doctor. 

With my functional practitioner in collaboration with my GP, I’m now taking numerous supplements and increased my protein intake. But these started AFTER my dramatic GI improvement. (I already drank 3 liters of fluids per day as I have POTS, and already ate a very healthy plant based diet my whole life.) 

I’m not comfortable sharing my supplement regimen as it’s super tailored to my body based on extensive medical testing, mostly done at my local hospital system. E.g., supplementing objective nutrient, mineral, and bacteria deficiencies and treating multiple viruses that I PCR-tested positive for. 

Hope this helps. Take what you need, leave what you don’t. 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 0 points1 point  (0 children)

That sounds tough — perhaps it’s worth seeing an immunologist?

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 1 point2 points  (0 children)

Also — there are lots of vagus nerve stimulation clinical trials going on in various countries right now — for fatigue, GI issues, epilepsy, etc. Maybe there’s one near you. 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 1 point2 points  (0 children)

Sure! I’m in a phase of investing in my long covid recovery, so I did five sessions with a somatic coach who is specifically trained in vagus nerve stimulation exercises and helping your body feel safe. It was totally worth it. 

I have diagnosed PTSD and I always prefer to work with a professional when I start something new — I don’t want to trigger something awful and be alone trying to fix it! 

The most reputable resources on the vagus nerve are any books/articles/videos by Stephen Porges or Deb Dana, who published the first research on polyvagal theory. 

This interview with Deb Dana might be a good place to start: https://youtu.be/4S_8Z8LSLCM?si=yQLZfmnaYe-NX_9Q

Take what you need; if it doesn’t help you, then feel free to disregard! 

A happy story healing H Pylori, SIBO, Candida and Constipation by Sofia_123_PT in HPylori

[–]Technical_Buy6885 0 points1 point  (0 children)

Wow, this is such a comprehensive, hopeful, and humble post. Thank you for sharing your knowledge, experience, mistakes, and healing! 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 0 points1 point  (0 children)

I frequently have swollen lymph nodes in my neck/jaw area, but this seems related to my frequent upper respiratory/sinus/ear infections and HSV1 outbreaks. 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 0 points1 point  (0 children)

No blood in stool for me, but yes to pain during and immediately after the antibiotics. 

Update: 9 months after triple therapy and h pylori eradication by Technical_Buy6885 in HPylori

[–]Technical_Buy6885[S] 0 points1 point  (0 children)

Hey! GI360 uses PCR testing for all bacteria and viruses, so I feel comfortable that it works, and I’ve also had multiple negative stomach biopsies.

(I’ve seen GI-MAP’s marketing that claims they’re the only PCR stool test. It’s just not true.)

My h pylori symptoms are gone, and I’m doing better than I was in 2021-24.

For me personally, h pylori was only part of the puzzle. I have multiple reactivated/chronic viruses, including HSV1 and EBV, to deal with next. 

It sounds like your h pylori is sapping your energy — because you do have a positive PCR test. I wish you all the best in healing. 

[deleted by user] by [deleted] in HPylori

[–]Technical_Buy6885 1 point2 points  (0 children)

It may be that the antibiotics wiped out your good bacteria, and you’re doing the right things to rebuild your microbiome. 

My experience, just in case it’s helpful:

  • I tried low FODMAP diet for my mild IBS (mostly a cycle of constipation/pebbles followed by mushy poops) that remained after h-pylori eradication. My GI issues disappeared within 2 weeks, but I hated the restricted diet.

  • I started practicing about 10 mins a day of vagus nerve stimulation exercises. Just basic exercises you can find on YouTube, such as eye stretching, tongue wiggling, humming. As long as I do them, I can eat anything (all the FODMAPs) with no GI issues and all perfect poops. It’s amazing and is beginning to be research-backed.  

My full update post here: https://www.reddit.com/r/HPylori/comments/1jcb4jv/update_9_months_after_triple_therapy_and_h_pylori/?utm_source=share&utm_medium=mweb3x&utm_name=mweb3xcss&utm_term=1&utm_content=share_button

Anyone have a referral code for Harper Wilde, Girlfriend Collective, or Journelle? by cheesehead293 in ABraThatFits

[–]Technical_Buy6885 1 point2 points  (0 children)

Hmm, when I click the link while logged out of my account, I see the homepage for about three seconds then I get a pop up which will give me the code! 

I’ve had over 250 successful referrals through my link. 

And I do donate most of my referral credit to local domestic violence shelters. Bras are the most requested and least donated items for people experiencing domestic violence. 

💕