So I’ve become the friendly neighborhood GLP hotspot 😅 anyone else?

Thee Oohwee

GLP-1 Apprentice
Member Since
Feb 25, 2026
Posts
89
Likes Received
252
Location
Los Angeles, CA
United-States
Hey all — could use some perspective from the forum.

I’ve been on Tirzepatide since October and it’s been a really positive experience for me. Naturally, a few close friends have gotten curious about obtaining their own from the grey market. A couple of them have done their own research and asked if I’d include them when I order, which I’m generally okay with.

Where I’m feeling a little more unsure is with my best friend.

He struggles with obesity and is also in recovery (like me). We’ve talked a lot about GLPs, and recently he decided he wants to give Tirzepatide a chance. I currently have more compounded meds than I can realistically use while I’m tapering off and moving to Reta, so I offered to share and help him start at a low dose.

One wrinkle: he’s triggered by handling syringes himself. So for now, the plan is that he comes by and I handle the injections.

Before moving forward, we looped in both of our sponsors and made sure everything was out in the open. No secrecy—just trying to be thoughtful and accountable about it.

He just started yesterday, but he’s already noticing the usual “food noise” quieting, and interestingly, some of the same mental calm I’ve felt too.

That said… I’m a little in my head about it. Part of me feels like, if something has helped me this much, how could I not help someone close to me access it? But I’m also aware there are some real boundaries here—medical, ethical, and recovery-related—and I don’t want to be naive about that.

So I’m curious:
Has anyone supported a friend or loved one starting GLPs?
How did you think about boundaries or your role in it—especially if recovery is part of the picture?

Would really appreciate hearing others’ experiences.
 
I debated whether to post this here or in a DM. I was going to DM it, but decided someone else may be able to get something out of it so decided to post it here.

So as a therapist, someone in long term recovery, and having worked in inpatient recovery for a long time, I'm going to share a somewhat controversial opinion. Triggers are bullsh*t. It's really not a helpful way to think about things. It is impossoble to avoid 'triggers'. When I was in a bad place, the sun coming up was a 'trigger'. There is always going to be another 'trigger'. When I'm where I need to be, none of it matters. Things are always going to be things that 'trigger' thoughts; you can't avoid it. The real question is do those thoughts have power? If he's in a good place, they won't and your fine. If he's new or hasn't got past that point, then focusing on recovery is better than focusing on weight.
 
Last edited:
I debated whether to post this here or in a DM. I was going to DM it, but decided someone else may be able to get something out of it so decided to post it here.

So as a therapist, someone in long term recovery, and having worked in inpatient recovery for a long time, I'm going to share a somewhat controversial opinion. Triggers are bullsh*t. It's really not a helpful way to think about things. It is impossoble to avoid 'triggers'. When I was in a bad place, the sun coming up was a 'trigger'. There is always going to be another 'trigger'. When I'm where I need to be, none of it matters. Things are always going to be things that 'trigger' thoughts; you can't avoid it. The real question is do those thoughts have power? If he's in a good place, they won't and your fine. If he's new or hasn't got past that point, then focusing on recovery is better than focusing on weight.
Thank you for sharing your professional and personal insight about "triggers" with me. I love getting new perspectives on my current ideas and belief systems - because I find that they often need work or have even been adopted from other people.

My friend has been in recovery for 12 years but had recently been having some "relapse ideations." He's working with his sponsor on those and I encourage him to stay grounded in his Twelve Step work. We go to several meetings together and we do service work.

He may reach a point - I'm fairly certain - where he can administer his own shots without a care in the world, much like I do now - as an ex IV drug user. My syringes don't bother me in the slightest. They are just tools for my health today and not my destruction.
 
My sister’s doctor stopped prescribing Rybelsus (oral Sema) about a year ago. She’d been on it for a year to lose weight and had dropped around 15 kg. But after stopping, she gained back about 10 kg, which felt terrible to her.

Meanwhile, after 5 months on prescribed Mounjaro, I was switching to grey market Reta. I told her about this and she asked if I could help her try that too—and I didn’t hesitate.
The first 2 pins I did for her and then I reconstituted her own little vial and sent her off with a set of syringes & swabs.

Fast forward 8 weeks: she’s down over 4 kg, and everyone’s happy 🙂

Soon I will be ordering her own little kit of Reta. The only thing that worries me is that she is starting to ask questions about ghk-cu and nad+ ...
🐇🕳️
 
My sister’s doctor stopped prescribing Rybelsus (oral Sema) about a year ago. She’d been on it for a year to lose weight and had dropped around 15 kg. But after stopping, she gained back about 10 kg, which felt terrible to her.

Meanwhile, after 5 months on prescribed Mounjaro, I was switching to grey market Reta. I told her about this and she asked if I could help her try that too—and I didn’t hesitate.
The first 2 pins I did for her and then I reconstituted her own little vial and sent her off with a set of syringes & swabs.

Fast forward 8 weeks: she’s down over 4 kg, and everyone’s happy 🙂

Soon I will be ordering her own little kit of Reta. The only thing that worries me is that she is starting to ask questions about ghk-cu and nad+ ...
🐇🕳️
It’s a slippery slope…
 
@Thee Oohwee As a recovering person for nearly 2/3 of my life, I don't buy into the concept of triggers. Recovery is all about reshaping thinking. If I haven't done that, I'm not recovering, I'm staying dry.

If they cannot manage an injection for their health, perhaps they're not ready. If he became diabetic and needed injection, what would he do? That's for him to solve.

His recovery and his life are his choices to make as they are for you and for me. I take hold of my choices and do not push my wishes onto others. It's lovely of you to have concern for his health. The best I can do is gently - and with kindness - express my concerns and identify solutions. The action is up to them.

Just like with the active alcoholic, I cannot get them sober. I can share my experience, strength, and hope. They have to show up and make changes. Food can also be an addiction. Treatement and a 12-step program are available.

Despite your very good intentions, I disagree to inject someone else. Especially another person in recovery. They, too, know the action is up to them.

We carry the message. We don't carry the alcoholic/addict.
 
Hey all — could use some perspective from the forum.

I’ve been on Tirzepatide since October and it’s been a really positive experience for me. Naturally, a few close friends have gotten curious about obtaining their own from the grey market. A couple of them have done their own research and asked if I’d include them when I order, which I’m generally okay with.

Where I’m feeling a little more unsure is with my best friend.

He struggles with obesity and is also in recovery (like me). We’ve talked a lot about GLPs, and recently he decided he wants to give Tirzepatide a chance. I currently have more compounded meds than I can realistically use while I’m tapering off and moving to Reta, so I offered to share and help him start at a low dose.

One wrinkle: he’s triggered by handling syringes himself. So for now, the plan is that he comes by and I handle the injections.

Before moving forward, we looped in both of our sponsors and made sure everything was out in the open. No secrecy—just trying to be thoughtful and accountable about it.

He just started yesterday, but he’s already noticing the usual “food noise” quieting, and interestingly, some of the same mental calm I’ve felt too.

That said… I’m a little in my head about it. Part of me feels like, if something has helped me this much, how could I not help someone close to me access it? But I’m also aware there are some real boundaries here—medical, ethical, and recovery-related—and I don’t want to be naive about that.

So I’m curious:
Has anyone supported a friend or loved one starting GLPs?
How did you think about boundaries or your role in it—especially if recovery is part of the picture?

Would really appreciate hearing others’ experiences.
Just as an aside, be careful.....you are opening yourself up to legal liabilities if your friends let your friendship pep-share out of the bag. If you end up selling some as a favor to someone and they f- it up somehow that results in medical Q&A....oh boy.
 
I can understand not wanting to be alone around syringes from an IV user’s perspective. An alcoholic would be foolish to hang out in bars to pass time.

Us recovering fatasses knew to not buy the tasty snacks so we wouldn’t eat the box in the first day. We still did it until peptides shut that part of our psyche off.


Until it becomes a legal issue for me, my general stance is it’s their decision that they’re responsible for, not me. As a child, I gave my mother allergy shots… no legal issue there.

If my “best friend” needed me to stick them, I don’t have a hangup with it. If they were an iv user in recovery I’d ask if they thought it through/consulted with their recovery folk. If they said yes, send it.

A random person wanting me to stick them? I’ll pass. Getting paid to stick is getting paid for unlicensed medical work, pass.


It also seems like Tirz could have meaningful therapeutic benefits towards his recovery.
 
Hey all — could use some perspective from the forum.

I’ve been on Tirzepatide since October and it’s been a really positive experience for me. Naturally, a few close friends have gotten curious about obtaining their own from the grey market. A couple of them have done their own research and asked if I’d include them when I order, which I’m generally okay with.

Where I’m feeling a little more unsure is with my best friend.

He struggles with obesity and is also in recovery (like me). We’ve talked a lot about GLPs, and recently he decided he wants to give Tirzepatide a chance. I currently have more compounded meds than I can realistically use while I’m tapering off and moving to Reta, so I offered to share and help him start at a low dose.

One wrinkle: he’s triggered by handling syringes himself. So for now, the plan is that he comes by and I handle the injections.

Before moving forward, we looped in both of our sponsors and made sure everything was out in the open. No secrecy—just trying to be thoughtful and accountable about it.

He just started yesterday, but he’s already noticing the usual “food noise” quieting, and interestingly, some of the same mental calm I’ve felt too.

That said… I’m a little in my head about it. Part of me feels like, if something has helped me this much, how could I not help someone close to me access it? But I’m also aware there are some real boundaries here—medical, ethical, and recovery-related—and I don’t want to be naive about that.

So I’m curious:
Has anyone supported a friend or loved one starting GLPs?
How did you think about boundaries or your role in it—especially if recovery is part of the picture?

Would really appreciate hearing others’ experiences.
Well this ticking more boxes than I thought I would read today. But to bottom line it, you control the "Spice" and the flow of it. I know playing Dr with a friend can be tough, as long as good intentions are at the heart of it, then hopefully no problems and you can sleep ok.

It took a while to get my friend on board with supplementing properly, eating better, etc. I told them they can go online and get it, blah blah blah if they don't like how I do it. I do have a plan, that if something happens to me. The spice will continue to flow, provide they don't go crazy with it.
 
Hey all — could use some perspective from the forum.

I’ve been on Tirzepatide since October and it’s been a really positive experience for me. Naturally, a few close friends have gotten curious about obtaining their own from the grey market. A couple of them have done their own research and asked if I’d include them when I order, which I’m generally okay with.

Where I’m feeling a little more unsure is with my best friend.

He struggles with obesity and is also in recovery (like me). We’ve talked a lot about GLPs, and recently he decided he wants to give Tirzepatide a chance. I currently have more compounded meds than I can realistically use while I’m tapering off and moving to Reta, so I offered to share and help him start at a low dose.

One wrinkle: he’s triggered by handling syringes himself. So for now, the plan is that he comes by and I handle the injections.

Before moving forward, we looped in both of our sponsors and made sure everything was out in the open. No secrecy—just trying to be thoughtful and accountable about it.

He just started yesterday, but he’s already noticing the usual “food noise” quieting, and interestingly, some of the same mental calm I’ve felt too.

That said… I’m a little in my head about it. Part of me feels like, if something has helped me this much, how could I not help someone close to me access it? But I’m also aware there are some real boundaries here—medical, ethical, and recovery-related—and I don’t want to be naive about that.

So I’m curious:
Has anyone supported a friend or loved one starting GLPs?
How did you think about boundaries or your role in it—especially if recovery is part of the picture?

Would really appreciate hearing others’ experiences.
I have introduced two of my sisters, my brother and several friends to glp1s and have helped them access it by sharing, and it's got its ups and downs. When they experience some of the not so pleasant side effects of these drugs it's not easy because I'm not a doctor and I don't have solutions. I explained to all of them what can happen, both good and bad, and told them they are responsible for doing their own research, but still some people are never happy.
 
If either my best friends had an addictive issue that was triggered by something otherwise innocuous, and their request for help was that they come by once a week and I handle the part that triggers, I would say yes without any issue at all, and certainly without trying to tell them how to manage their addiction. These are people I love dearly, and it's so little to ask; I'd do much more work than that if it was helpful to them, and why on earth have dearly loved ride or die friends if not for the fact that sometimes one has something they can help the other with that doesn't cost much time, money, or effort? Neither of them have ever or will ever pay for any of the things I make, which I won't list because it would dox me, but "you will never have to buy X again because I make it" is a thing with my dearest friends, so five minutes on a visit wouldn't even make me blink.

EXCEPT. Not this. Nobody should be injecting ANYBODY else with grey, hard stop.

This isn't equivalent to "the spoon I use to stir this thing once a week has some psychological risk for me, is there any chance I could stop by once a week and you stir it for me?" "Of course, what day do you want to do it?"

If either of my bff's brought over something, and I swabbed the top, wiped their skin with alcohol, pulled the right number of units, and injected it into them, and they had some kind of reaction and god-forbid died from it (allergy, bad stuff, something), I would stand an excellent chance of going to prison; because as far as I know, grey stops being semi-legal the second your inject it into anyone.
 
Could a middle ground solution be for them to buy their own grey, you deliver a syringe to their house once a week, wait in the car while they inject, and collect the syringe when they are done? That way you would not be liable for delivering the drug to them? (Actually idk what that would mean legally mean if you just provided the needle and not the drug).

Anyways, it's up to you if it's worth this much trouble to help your friend. Just thought I'd offer an idea.
 
Interesting that a number of us have friends like this. The one person in my life that knows I'm on grey peps is a friend who is taking compounded sema. She was prescribed the brand name when she had a job with that insurance but after that one ended she's been doing medspa compounding.
When I finally got a handle on doing my own at home going light grey (I was getting from Modern Peps and a few others paying $$$ before finding Cain) and felt comfortable reconning vials, she wanted to try, as well. I was fine with making the purchases of the peps, and gave her links to get the syringes and bac water, and had her over one day to go through the process. I sent her the same videos that I used when learning, as well as a few online dose calculators.
The problem I discovered was two fold: 1) she used to live with heroin addicts and the syringes "triggered" her so she really doesn't want to have them around and pull from vials, etc and 2) she said she'd forget and it was all too confusing and wanted me to prep vials and syringes for her.
She's a really good friend, but I had to gently say no. As folks here have posted, I am not a doctor let alone not hers, and I will not take responsibility for anything remotely as invasive as this. She was obviously disappointed and a little hurt, but I was honest and told her she needed to either work on her ick of the syringes and recognize what they can do for her here and now, (she wasn't using the H, she was just around people who did a lot) or just keep paying the compounding places to do it for her.
Also, for the second note, with her seeming confusion: she's a smart woman and I know for a fact she could figure it out just as I had and get the hang of it pretty quickly. However, she also can play the flustered, helpless card now and then when she's presented with a challenge.
Bottom line: I was not about to be her personal supplier, handing over pre-filled syringes, and telling her what doses to take, etc.
I fall in the camp of "this is an area where I will adamantly stand by a DIY policy.
 
I think @5byfive makes a great point about triggers. However, you mentioned that your friend has been having relapse ideations lately, so that makes it a little more precarious.

Still, tirz is known to help with addiction. Perhaps once your friend gets to their maintenance dose, it won't be a problem.

Depending on the person, and how much I trust them not to point the finger at me if something goes awry, I think I would help them with injections up until they reach maintenance dose. At that point, hopefully they won't be triggered, but a plan should be in place in case they are, which doesn't include doing the injection for them.

Of course, as others have mentioned, you both have to be fully aware of the legal liabilities, willing to accept them, and risk the consequences.
 
Depending on the person, and how much I trust them not to point the finger at me if something goes awry...
When things go awry - for whatever reason - it doesn't matter how good the relationship was at any point in time. This is a recipe for disaster.

I provide educational resources with the caveat that there are many more resources available and they have to decide for themselves. For friends who have asked me to assist them with the product(s) they want, I will also give them starter supplies, including filters.
 
Thank you everyone for this open and honest discussion. I have a lot to think about.

I will say that I am definitely in the camp of having my friend begin his own pep education. I'll direct him to the appropriate links so he can begin to get his own knowledge on it. And I'll discuss it with him straight-up that we need to get him to a place where he can keep his kits at home and do his own shots. However, I will let him know that I can always come and be present on pinning day as he gets used to it.
 
I told my sister what I am doing and I told her that I do not want her to do it. I don't want anything to happen to her because of something I led her to. And there has been way too many issues since I have started October 2025 with failed sterility and very high endos I do not want to be responsible for anything happening to her.
 
It was my mom who got me to look into this gray market. There were some people in my family already in it. I decided to become the expert, and now I'm the one educating everyone around me and placing orders for others. Also, every time I speak to someone who is on it and complains about the price, I have a little convo with them.
 
I can understand not wanting to be alone around syringes from an IV user’s perspective. An alcoholic would be foolish to hang out in bars to pass time.

Us recovering fatasses knew to not buy the tasty snacks so we wouldn’t eat the box in the first day. We still did it until peptides shut that part of our psyche off.


Until it becomes a legal issue for me, my general stance is it’s their decision that they’re responsible for, not me. As a child, I gave my mother allergy shots… no legal issue there.

If my “best friend” needed me to stick them, I don’t have a hangup with it. If they were an iv user in recovery I’d ask if they thought it through/consulted with their recovery folk. If they said yes, send it.

A random person wanting me to stick them? I’ll pass. Getting paid to stick is getting paid for unlicensed medical work, pass.


It also seems like Tirz could have meaningful therapeutic benefits towards his recovery.
+1 for Tirz helping with recovery. A close friend stopped taking oxycodone after being on it 15yrs when he got on Tirz. He's been off it but still on Tirz 1 year next month. Pretty impressive to me! Obviously it still took constant effort on his part but he said the Tirz made it much more possible. Whether that's true for all idk but we will take the win.
 
Last edited:
Thank you everyone for this open and honest discussion. I have a lot to think about.

I will say that I am definitely in the camp of having my friend begin his own pep education. I'll direct him to the appropriate links so he can begin to get his own knowledge on it. And I'll discuss it with him straight-up that we need to get him to a place where he can keep his kits at home and do his own shots. However, I will let him know that I can always come and be present on pinning day as he gets used to it.
I’m open about my GLP use. After losing 50lbs people will ask. I started compound tirzepatide through a Telehealth outfit last Aug. (still using it BTW). For people who want to begin GLPs for themselves, and can’t get a Dr’s or insurance approval, I steer them in that direction. Once they have their own script I’m willing to share more.
 
Thank you everyone for this open and honest discussion. I have a lot to think about.

I will say that I am definitely in the camp of having my friend begin his own pep education. I'll direct him to the appropriate links so he can begin to get his own knowledge on it. And I'll discuss it with him straight-up that we need to get him to a place where he can keep his kits at home and do his own shots. However, I will let him know that I can always come and be present on pinning day as he gets used to it.
THAT is reasonable. Also, if it comforts him; you can get lockable ammo box for like ten bucks on Amazon, and a lock with a timer on it from same. Pin, put your syringes in it, set the timer, and that box is staying closed for seven days. I still cannot be trusted with cookies in the house, so I have one that I keep cookies in.
 
I have a very close friend, basically a sister, and she’s one of the only people I told about the grey. She kept asking how I’d lost weight, and I didn’t want to lie: she had a failed sleeve and was really struggling. In Italy the body shaming is brutal.

I explained everything clearly, risks and heavy side effects, and she was scared, as she should be.
But after seeing my results, she wanted to try. I just asked her to get full bloodwork. She understood the risks, so I didn’t step back.

She’s happy now, and I don’t regret sharing info and purchases with her.
She made her own choice.
I’d never discuss this with acquaintances, coworkers, or people who aren’t truly close.
 
No way. The possible repercussions....just too many. For instance, what if you shared your Tirz and they had a serious reaction ☠️to high endo levels even though you didn't? Would you be at fault? I'd say yes. What if they did one of the dumb things and od? IT's too risky. Your heart's in the right place but it won't be your heart in a court room. Advice from personal experience. That's all you should be giving. Point them to this place.
 
If it were me, I’d point him to Reddit and the tirzepatidecompound sub. At the top is a where to buy of telehealths. He should get an active script. Make him go the above board route. This would help take away some of the “questionable” stigma away for a previous user.

When he’s a ways in you can always offer to point in this direction but leave it up to him.

I’d personally detach from that situation for liability reasons.
 
Hey all — could use some perspective from the forum.

I’ve been on Tirzepatide since October and it’s been a really positive experience for me. Naturally, a few close friends have gotten curious about obtaining their own from the grey market. A couple of them have done their own research and asked if I’d include them when I order, which I’m generally okay with.

Where I’m feeling a little more unsure is with my best friend.

He struggles with obesity and is also in recovery (like me). We’ve talked a lot about GLPs, and recently he decided he wants to give Tirzepatide a chance. I currently have more compounded meds than I can realistically use while I’m tapering off and moving to Reta, so I offered to share and help him start at a low dose.

One wrinkle: he’s triggered by handling syringes himself. So for now, the plan is that he comes by and I handle the injections.

Before moving forward, we looped in both of our sponsors and made sure everything was out in the open. No secrecy—just trying to be thoughtful and accountable about it.

He just started yesterday, but he’s already noticing the usual “food noise” quieting, and interestingly, some of the same mental calm I’ve felt too.

That said… I’m a little in my head about it. Part of me feels like, if something has helped me this much, how could I not help someone close to me access it? But I’m also aware there are some real boundaries here—medical, ethical, and recovery-related—and I don’t want to be naive about that.

So I’m curious:
Has anyone supported a friend or loved one starting GLPs?
How did you think about boundaries or your role in it—especially if recovery is part of the picture?

Would really appreciate hearing others’ experiences.
It amazes me that it's always the man that's the crybaby. Don't hear a peep out of women. I guess that's why they have the babies.

I was gonna do a review on Fox04 which is great. However it did burn and itch me for several hours each time. Since that would "trigger" some dude to take 15 pictures of his red spot from the pin I decided not to.
 
I get why you want to help him, especially if this has been life changing for you. That part makes total sense.

But you’ve stepped into a role that really isn’t yours to carry. Sharing and administering something like this puts you in the position of prescriber, pharmacist, and provider all at once, and that’s where this starts to get risky fast.

The recovery piece makes this more complicated, not less. Even if the medication itself isn’t addictive, the dynamic of you controlling access and giving the injections can create dependency in a different way. That’s not a small thing.... For either of you.

Also, if he’s triggered by handling syringes, that’s important information. The solution shouldn’t be you doing injections for him indefinitely, it’s finding a setup where he can safely and independently manage his own care.

You’re not wrong for wanting to help, but helping doesn’t have to mean being the everything. A better lane is supporting him in getting this prescribed through a legitimate provider who will dictate medical decisions. If sourcing is impossible bc of insurabce/costs.... You could help him navigate access, and then be there for accountability.😉

Right now you’re taking on medical, ethical, and personal risk that doesn’t really belong to you.
 

Trending Topics

Forum Statistics

Threads
18,069
Posts
188,221
Members
60,591
Newest
soft.corruption
Back
Top Bottom