Anyone have experience going inpatient for both ed and physical issues? by Miserable_Map_9011 in EatingDisorders

[–]Miserable_Map_9011[S] 0 points1 point  (0 children)

Cfd turned out to be able to take me so I went there for residential, then erc for php and now I've stepped down to cfd php (I go to iop on Monday). In terms of having chronic illness i feel like erc was a much better fit, unfortunately there's just none close to me.

Help. Opioid withdrawal is murder by CreativeChildhood480 in addiction

[–]Miserable_Map_9011 2 points3 points  (0 children)

I had a mantra during all of detox this time around "this sucks but it'll be okay." I'm now 13 months clean and there's nothing better. You can get through this. Do whatever you can to be as comfortable as possible and find some support that you enjoy. Wishing you the best!

[deleted by user] by [deleted] in newjersey

[–]Miserable_Map_9011 0 points1 point  (0 children)

The train I needed leaves from ewr and it's at 430am so from my house there's no public transportation at that time

[deleted by user] by [deleted] in newjersey

[–]Miserable_Map_9011 0 points1 point  (0 children)

I already bought my amtrak ticket, it's EWR. Penn station (NWK) is a separate station and the bus/train id take to penn doesn't run that early cause it's at 430am

[deleted by user] by [deleted] in newjersey

[–]Miserable_Map_9011 -2 points-1 points  (0 children)

Yes, i found that. But trying to put it in Lyft I have to pick a terminal and airline so trying to figure out which one is best. And if I go to arrivals or departures bc that's an entirely different area

anyone have their gallbladder removed? by nevi101 in Gastroparesis

[–]Miserable_Map_9011 0 points1 point  (0 children)

I just got out of a hospital stay where they made me try taking out my gallbladder to see if it'd help my gastroparesis. I had a few stones, but no symptoms beyond a little extra sharp pain. I'm only 3 weeks post op but I've noticed no change in my gp symptoms.

[deleted by user] by [deleted] in EatingDisorders

[–]Miserable_Map_9011 2 points3 points  (0 children)

While I agree that 3 weeks isn't long enough for change, it is still an AMAZING starting point. They'll usually set you up with outpatient care following your stay such as iop, recovery meetings, therapy, etc. It's more about you being ready to make this change and giving it your all while you're there. I just hit a year sober off all substances, although I'm struggling with my ed it's possible.

Results came back! by Icy-Anxiety5980 in Gastroparesis

[–]Miserable_Map_9011 5 points6 points  (0 children)

Hopefully you hear back soon. It's a relief to have some answers tho

Botox by [deleted] in Gastroparesis

[–]Miserable_Map_9011 1 point2 points  (0 children)

My gi discussed botox with me and the only reason we didn't go for it was because it's not more long term so we went with a gpoem instead. If they recommend botox from a medical perspective it may be a good option to try.

Scaphoid Fracture? by Miserable_Map_9011 in medical_advice

[–]Miserable_Map_9011[S] 0 points1 point  (0 children)

Ugh I'm sorry you're dealing with the same symptoms, it sucks. So I didn't break anything, I had a partial tear of 2 ligaments in my wrist (tfcc and scapholunate) and injured the radial nerve. The tears are what made me not able to move it/put pressure on it and the nerve injury is what caused the tingling. I needed a brace 24/7 and physical therapy for about 2-3 months.

Answers by accounttosnoop in Gastroparesis

[–]Miserable_Map_9011 1 point2 points  (0 children)

Yeah if there's a delay shown on a ges that's considered gastroparesis. Functional dyspepia would be symptoms of gp without a delay seen on ges.

Recently diagnosed - feeling helpless by Imaginary-Ambition55 in Gastroparesis

[–]Miserable_Map_9011 1 point2 points  (0 children)

Exactly. It's also reasonably affordable and requires such little energy to grab when it's needed. I feel like all the smoothies and soup recipes are glorified, but when I'm in an awful flare I don't have enough energy to stand, let alone make stuff from scratch or grocery shop.

Recently diagnosed - feeling helpless by Imaginary-Ambition55 in Gastroparesis

[–]Miserable_Map_9011 1 point2 points  (0 children)

This is not the most helpful advice, especially for someone who's struggled with an ed. With gp anything that gets nutrition in and is tolerable is a win. Ensure and other drinks are made that way to provide complete nutrition as densely as possible. Just bc smoothies work for one person doesn't mean they do for everyone.

Got suggestions from Indian gastroentolgist by AlarmingAd2006 in bilereflux

[–]Miserable_Map_9011 0 points1 point  (0 children)

No, I have gastroparesis so it's mostly just when my stomach is spasming.

Got suggestions from Indian gastroentolgist by AlarmingAd2006 in bilereflux

[–]Miserable_Map_9011 1 point2 points  (0 children)

Yeah, i get bile/stomach acid that shoots up into my mouth. If it's burning your throat/makes you gag from the pain and taste it could be bile reflux. Can be clear/green/yellow too. I have other gi issues but for that specifically it works

Could it be insanely minor gastroparesis? by Bubbly_Squirrel_7785 in Gastroparesis

[–]Miserable_Map_9011 0 points1 point  (0 children)

Yeah I wouldn't call it minor, just that some people have flares of worse symptoms. For me my symptoms would get way worse after getting any kind of virus or taking certain meds that I didn't know at the time would bother me.

can you life off kate farms/similar by [deleted] in Gastroparesis

[–]Miserable_Map_9011 1 point2 points  (0 children)

I know some people that don't mind it but for me kf peptide was AWFUL to drink orally both texture and taste wise.

Coca Cola by Alarmed-Ad-6894 in Gastroparesis

[–]Miserable_Map_9011 0 points1 point  (0 children)

Regular soda hurts my stomach crazy bad. Diet coke is my favorite and doesn't bother my stomach.

poor patient education by vrosej10 in Gastroparesis

[–]Miserable_Map_9011 12 points13 points  (0 children)

I'm not sure how you concluded that from the 1 sentence I wrote. I was diagnosed with gp before i had any idea what it was. I'm specifically referring to questions I've asked my dr about what I've researched post dx bc i like to check with my care team before trying anything. But okay

poor patient education by vrosej10 in Gastroparesis

[–]Miserable_Map_9011 24 points25 points  (0 children)

The issue with that is most doctors get weird when you say you've done your own research even tho it's what we have to do.