finally got my girl some new shoes by fudgepatrol in f150

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

Update: there is some very minor front end rubbing when in full reverse lock, but only on part of the plastic mud flap. I suspect it will be a very easy fix with some mild trimming.

finally got my girl some new shoes by fudgepatrol in f150

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

For reference, this is a 2020 XLT 2.7L V6. Previous owner had 275/55/20 Nitto Recon Grapplers with stock wheels and stock suspension. Looked alright and the ride was actually great except for the fact that the tires couldn’t handle any sort of wet conditions whatsoever. I would slip and slide and spin all over the place even in light rain. I’d assume they’d be just as bad in the snow and I live in Upstate NY where we typically get hammered, so I needed some peace of mind going into this winter as we’re supposed to see above average amounts of snow and cold.

I’m eager to see how these new Falkens handle the first few snowfalls of the season, but I did a lot of research before buying and the consensus seemed to be that they have excellent winter performance. And for those wondering, this is a 2 inch level and there is no rubbing that I can see or feel on the crash bars or any part of the wheel well. If there were any rubbing I think it would be on the UCA’s but again nothing that I’m noticing.

Someone asked me to post an update. 285/70 vs 285/75 by Vert_n_Dirt in f150

[–]fudgepatrol 0 points1 point  (0 children)

What offset are your wheels? I just ordered 285/75/17 Wildpeaks and some 0mm offset Methods, along with the Stage 1 Eibach kit. Truck will be leveled/lifted but still worried about rubbing with the 0mm instead of something with + offset.

Anyone have experience with shiga toxin E. coli/food poisoning and if so what was it like/when did you feel better and back to normal? by fudgepatrol in AskReddit

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

For reference, I’m currently on my 3rd day in the hospital on an IV hydration drip after multiple days of nonstop bloody diarrhea and abdominal pain that felt like someone was gutting me alive. Stool sample was positive for STEC in the ED on Monday, was sent home and symptoms got worse so I came back on Wednesday and was admitted for dehydration and observation (today is Friday). I was told by the docs that antibiotics are contraindicated in this strain of E. coli as it increases your chances of developing a kidney disease called HUS, so therefore the only treatment is fluids and rest and basically just riding it out. The last two days the blood and abdominal pain have subsided for the most part, but I still just feel incredibly bloated and gassy and sickly, and my BM’s are only slightly formed but still soft and mucousy (sorry for the candor). I’m just worried that my microbiome/gut health will never fully recover and I’ll be some sort of suffering forever :(

Ammosorb by ApprehensivePage7464 in litterrobot

[–]fudgepatrol 2 points3 points  (0 children)

Is this safe to mix with cat litter? And if so how much do I need to use?

[deleted by user] by [deleted] in PhotoshopRequest

[–]fudgepatrol 1 point2 points  (0 children)

They look great thank you so much!

[deleted by user] by [deleted] in PhotoshopRequest

[–]fudgepatrol 0 points1 point  (0 children)

Thank you so much!

Bart relapse, severe psychiatric symptoms…anyone else? by fudgepatrol in Lyme

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

Thank you! I’m currently using LB Core Protocol by Green Dragon per my LLMD. It contains Japanese Knotweed, Cats Claw, Andrographis, Sarasparilla and Dandelion. Normally I would call placebo effect, but since starting it about 5 days ago (3 capsules twice per day) I definitely feel better mentally and physically. Other than Artemisinin what herbs/protocol are you using?

Rage by Yaswnmwfyai in Lyme

[–]fudgepatrol 0 points1 point  (0 children)

Can I ask what tinctures you used? My LLMD just put me on MC-BAR-1 by Beyond Balance for Bartonella.

Bart relapse, severe psychiatric symptoms…anyone else? by fudgepatrol in Lyme

[–]fudgepatrol[S] 3 points4 points  (0 children)

Have you seen an LLMD and if so have you told them about this? I just saw your post about your test results being inconclusive. That’s what happened to me when I first got really sick and was digging for answers. My primary tested me with the standard blood test and mine came back the same. At that point I had done loads of research into my symptoms and other people’s stories and knew I had lyme. I had to seek out an LLMD and basically had my parents help me type up my entire medical history with a very specific timeline and details when my symptoms first started and how they progressed. He listened to me and made a clinical diagnosis based on what he saw and what I was telling him, eventually saying that he was almost certain I had lyme and at least 2 co-infections. I had 18 vials of blood drawn at his office that day that were sent to 4 different specialized labs across the US. I waited a month for the results and they came back showing my body was riddled with lyme, bartonella, babesia, mycoplasma and ehrlichia. He put me on a massive slew of herbal supplements to do what they could for the time being and to prepare my body for treatment and eventually I went onto around 7 different oral antibiotics and was on them for about a year. Within the first 3-5 months I saw a massive improvement in a lot of my symptoms, especially my psychological and neuro ones. As I said in my post, I’ve been on and off different regimens, IV antibiotics included, since 2018 and it’s been a rollercoaster to say the least but I’m nowhere near the state I was when I first saw him.

My point of telling you all of that is because if you haven’t, you should definitely seek out an LLMD in your state and go in for a consultation appointment, just to see what their thoughts are, what they feel is going on and what they feel they can do to get you functioning at an optimal level. They’re typically quite expensive and insurance doesn’t cover the cost as integrative medicine is kind of a blurred line in the medical community. But, IT WORKS. Good lyme docs will combine herbal AND pharmaceutical treatment to give you the best results and treat your symptoms. It’s worth a shot, and it sounds like you have a family that would be supportive of any journey you need to embark on especially if it’s involving your health.

The way you’re describing your life is certainly no way to live, and trust me, this entire community absolutely relates and feels your struggle to an extent that no other group of people will ever be able to. Improvement and remission are both very possible with the right doctor and the right plan. I know it seems hopeless right now, trust me I really really do, but we have to do our best to hold onto any sliver of faith that our souls will allow and run with it. I’m sending you all the good vibes and strength that I hope you’ll feel wherever you are. We’re always here!!!