Cat-a-Tonic
Super Moderator
- Joined
- May 5, 2010
- Messages
- 12,651
This is pretty personal which is why I'm posting it in here. I've got a friend, my best friend actually, at least I thought she was. Lately some things have been nagging at me and I think I've caught her in a few lies (that's what I need clarification about). Well, to be blunt I've definitely caught her in a few lies and possibly in a few others. I'm starting to suspect she might be a pathological liar. She says she's got Crohn's, and I want to believe her, but things are really starting to nag at me.
She said the other day that she's "been taking Remicade at night" and that it's really helping. But I thought Remi was an infusion that you get in a hospital infusion center type setting every 8ish weeks? There's no way you'd "take it at night", right? I mean, you'd have to take it during the hours that the infusion center is open, and that wouldn't be at night? Just the way she phrased it, it sounded fishy to me. Can someone with Remi experience please clarify for me?
Another thing that bugs me, she's (supposedly) been on Remicade for awhile, but at one point during the summer she said her doctor wanted her to try Cimzia. I asked if she was doing the shots on herself, since I know from the forum that Cimzia is an injection. She said that there's another version of Cimzia available which is an inhaler and she did that because she doesn't like shots. But she didn't last long on Cimzia because she "liked Remicade better". Now, I did some googling, and I couldn't find anything at all about an inhaled version of Cimzia. I haven't seen anything on the forum about that either. People with Cimzia experience, can you tell me if it's just an injection/shot or if there's an inhaled version?
There's been other stuff too. Mainly little stuff like, one day she'll complain about the bitter taste of Zantac, but the next week when I'm taking my meds in front of her and I also talk about how I hate the taste of Zantac too, she'll ask me what it tastes like - seriously, I know that you know what it tastes like because you talked about it before!
One particularly big lie, possibly the biggest - when I first met her, we bonded right away because I had only been ill for a few months and I told her that my doctor thought I might have Crohn's. She said, "My mom has that!" And we bonded further when she got diagnosed herself a few months later. But just the other day, we were talking about her mom, and about Crohn's, and she muttered, "My mom's just lucky she doesn't have it herself." What???? So does your mom have Crohn's or not? That was what I thought but couldn't say it. I was so shocked I just stared at her and haven't confronted her yet about that lie. It's like, is our entire friendship and bonding based on a lie?
My friend is, besides the lies, a good friend - she's been really supportive of me and is very sweet, can make me laugh, etc. I don't know what to do, and I don't know if confronting her about this stuff will end our friendship. I don't have many friends and she's my only Crohnie pal - but is she even a Crohnie? I really don't know anymore. She says she is but can I believe anything she says? I'm so conflicted and confused. Can anyone help me?
She said the other day that she's "been taking Remicade at night" and that it's really helping. But I thought Remi was an infusion that you get in a hospital infusion center type setting every 8ish weeks? There's no way you'd "take it at night", right? I mean, you'd have to take it during the hours that the infusion center is open, and that wouldn't be at night? Just the way she phrased it, it sounded fishy to me. Can someone with Remi experience please clarify for me?
Another thing that bugs me, she's (supposedly) been on Remicade for awhile, but at one point during the summer she said her doctor wanted her to try Cimzia. I asked if she was doing the shots on herself, since I know from the forum that Cimzia is an injection. She said that there's another version of Cimzia available which is an inhaler and she did that because she doesn't like shots. But she didn't last long on Cimzia because she "liked Remicade better". Now, I did some googling, and I couldn't find anything at all about an inhaled version of Cimzia. I haven't seen anything on the forum about that either. People with Cimzia experience, can you tell me if it's just an injection/shot or if there's an inhaled version?
There's been other stuff too. Mainly little stuff like, one day she'll complain about the bitter taste of Zantac, but the next week when I'm taking my meds in front of her and I also talk about how I hate the taste of Zantac too, she'll ask me what it tastes like - seriously, I know that you know what it tastes like because you talked about it before!
One particularly big lie, possibly the biggest - when I first met her, we bonded right away because I had only been ill for a few months and I told her that my doctor thought I might have Crohn's. She said, "My mom has that!" And we bonded further when she got diagnosed herself a few months later. But just the other day, we were talking about her mom, and about Crohn's, and she muttered, "My mom's just lucky she doesn't have it herself." What???? So does your mom have Crohn's or not? That was what I thought but couldn't say it. I was so shocked I just stared at her and haven't confronted her yet about that lie. It's like, is our entire friendship and bonding based on a lie?
My friend is, besides the lies, a good friend - she's been really supportive of me and is very sweet, can make me laugh, etc. I don't know what to do, and I don't know if confronting her about this stuff will end our friendship. I don't have many friends and she's my only Crohnie pal - but is she even a Crohnie? I really don't know anymore. She says she is but can I believe anything she says? I'm so conflicted and confused. Can anyone help me?