u/Jinxie1206

▲ 3 r/Pets

Health insurance companies

Hello! I adopted a little 5 month old puppy and I am looking for good insurance. I lost my dog a year ago and I had Odi/ManyPets and I was wondering if anyone here has any recommendations? Odi kind of sucks and I’m overwhelmed with all the companies out there.

Any advice or recommendations would be very appreciated!

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u/Jinxie1206 — 2 days ago
▲ 42 r/lupus

House M.D.

So, let’s talk about the show House. How do you people feel about it? I have mixed feelings since yes it has brought attention to the disease but not exactly the attention that lupus should get. Sometimes when I mention I have it people will ask me if it’s really lupus. Sometimes I laugh but other times it gets annoying. Someone one time asked me if it was a real disease or if it was made up by the show creators. I didn’t get mad because the person seemed to be genuinely confused so I explained to them that yeah, it does actually exist.when I told my brother that I was diagnosed with lupus he sent me a meme of House. Since it’s my brother I laughed and thought that it was funny. What do you guys think?

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u/Jinxie1206 — 7 days ago
▲ 40 r/lupus

Ok so I’ve been part of this forum since I was diagnosed about a year ago. I really like this community. I have been given good advice and encouragement. There have been various discussions but I have yet to see one about intimacy and sex.

I am not asking for specific information or details. I was just wondering how this disease has affected you and your partners. Do the symptoms make it hard for you to be physically intimate with your partner? If you have faced challenges how did you deal with them?

I currently do not have a partner but I would like to be with someone in the future. I am afraid that the symptoms that I experience will make that difficult. The joint pain alone makes it hard to move so I can only imagine what it will be like to position myself for the activities. I do enjoy being intimate but I’m afraid of how my lupus will affect it as well as my partner. How did you tell your partner about your lupus? How did you explain that you might not be able to do certain things? How did you deal with the physical challenges?

Again I’m not asking anyone to go into detail about their sex life. I’m just curious because I have yet to read a post about this topic.

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u/Jinxie1206 — 15 days ago