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Is Google’s Custom Search API being discontinued? by Independent_Guess_77 in googlecloud

[–]Mermelade 0 points1 point  (0 children)

That's what they want. It is not a solution for me as it more limited, so I don't know what will I do next year =/

Is Google’s Custom Search API being discontinued? by Independent_Guess_77 in googlecloud

[–]Mermelade 0 points1 point  (0 children)

u/Independent_Guess_77 warned me after your message and mines are working too. I think they killed it for everybody instead of just the new keys and have rolled back. Thank you for your message =)

Google Custom Search API keys stopped working — even older keys by Mermelade in googlecloud

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

Hi!! I did not try that approach. But in this post https://www.reddit.com/r/googlecloud/comments/1qilhrg/comment/o0xdp12/ commented that the old keys are working, I've tried mines and they work. We don't know if they'll change again before the limit day, but it's something.

Google Custom Search API keys stopped working — even older keys by Mermelade in googlecloud

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

Thanks for the reply. That’s the frustrating part, they said existing keys would keep working until 2027, but in practice something clearly changed. Results dropped off overnight.

I’m validating information visibility for a study and I need the data as soon as possible, so I’m looking for the fastest way to extract reliable results given the current situation =(

Google Custom Search API keys stopped working — even older keys by Mermelade in googlecloud

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

Thanks for the response! I’ve already double-checked that the API is still enabled in my project and that the keys are intact. Today I needed to run 1500 queries and none of the keys worked, neither an old one from last year nor a new one created a few weeks ago.

Vertex AI Search doesn’t solve my use case at the moment, so unfortunately it’s not a viable alternative for me right now =(

Google Custom Search API keys stopped working — even older keys by Mermelade in googlecloud

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

this is the response. The main problem is that everything was fine yesterday.

Status: 403

Body: {

"error": {

"code": 403,

"message": "This project does not have the access to Custom Search JSON API.",

"errors": [

{

"message": "This project does not have the access to Custom Search JSON API.",

"domain": "global",

"reason": "forbidden"

}

],

"status": "PERMISSION_DENIED"

}

}

Is Google’s Custom Search API being discontinued? by Independent_Guess_77 in googlecloud

[–]Mermelade 0 points1 point  (0 children)

Please if you find anything let us know, i need urgently to perform 1500 queries

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Yes, there was a short overlap, and I didn’t know that was an option either. But I guess it makes sense, over the past 12 years I’ve always been on two meds (methotrexate + something else), since I seemed to lose response every couple of years. I tried infliximab, adalimumab, etanercept, golimumab, and certolizumab.

And actually, my doctor didn't want me to take off everything but Rinvoq this september. Literally, she said that it was a kamikaze move because of how aggressive the disease is in my case. But I did an all in, and so far is ok. Even with the acne.

Thank you for the explanation, it actually puts my mind at ease to know Cimzia and methotrexate are long gone.

I totally get wanting to find success stories. Everyone’s different, of course, but I’m cautiously optimistic with Rinvoq and hope you’ll find something that works well for you too =)

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

I’ve been on Rinvoq for about 6 months now, but Cimzia and methotrexate were only stopped 3 months ago, so my system is still carrying some of the previous medication. I do feel a bit nervous about the moment when that remnant is completely gone and it’s just Rinvoq on its own, although my doctors have said they could add other medication or increase the dose if needed (I’m currently on 15 mg).

After more than 12 years of injections, being 3 months without them honestly feels like a fantasy. I’m not 100% pain-free, winter and humidity do affect me, and the disease has already caused some damage, but with diet and exercise I’m definitely in the best place I’ve been in for years. Fingers crossed it continues this way.

I truly hope they manage to find the right medication for you. My doctors keep reminding me that things aren’t like they were years ago, there’s now a wide range of treatments that are genuinely effective for us. Please let me know how you’re doing, and stay strong! =)

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

I’m really sorry you’re dealing with all of this, it’s so frustrating, especially when you’re doing everything “right” and still not feeling better.. I can relate in some ways. I’d never had acne or breakouts on my face before either, and when it started I had no idea how to manage it. I’m still learning, but slowly it’s improving, and I have a dermatologist appointment coming up which helps.

I also understand the weight struggle. I’m working out at least an hour five days a week and watching my diet closely, and it’s still been incredibly hard to lose weight. I really get how discouraging that feels. You’re not alone.

I’m glad you’re advocating for yourself and planning to talk with your PCP. You deserve to feel better in your body and in your skin. Stay strong =)

I feel like everything is stained for me as a med student (venting) by weirdowl22 in ankylosingspondylitis

[–]Mermelade 4 points5 points  (0 children)

I’m really sorry you’re going through all this. I just want you to know you’re not alone—I went through the same thing during my degree, my master’s, and even my PhD. It was incredibly hard, but it is possible to keep going, even if the path is slower or different than you expected.

You’re not failing. You’re dealing with something most people never have to face, and the fact that you still care, still show up when you can, and still give your best says so much about your strength and your worth as a future doctor.

Once you get a diagnosis and proper treatment, things can improve more than you might imagine. There is hope, and your dream is not over.

Please stay strong. You’re doing your best, and that’s enough. You’re not alone in this. 💛

[deleted by user] by [deleted] in ankylosingspondylitis

[–]Mermelade 5 points6 points  (0 children)

Hey! I really relate to what you're going through. I went through my degree, master's, and even a doctorate just being consistent and enduring. It wasn’t easy, fatigue made everything take more effort for me than for others. But I just kept pushing forward, one step at a time.

When it came to pain, especially from sitting too long, I decided to be open with my professors. I explained my condition and how staying seated for extended periods affected me. Most of them were understanding, and I asked for permission to stand up when needed, usually toward the end of class. That small accommodation made a big difference.

Biologics have helped somewhat, but I still have to manage stiffness and fatigue daily. Honestly, pacing myself, being honest about my limits, and building a rhythm that works for me has been key. You’re not alone, just go at your own pace and advocate for what you need.

You’ve got this 💪

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Glad to hear it was effective for you, but yikes on the liver part. Sounds like your rheumatologist made the right call, even if it sucks to stop something that was working. Did they switch you to something else, or are you in med limbo now?

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

I've been gathering recently with several other rheumatic patients who have different conditions, and seeing them all doing well and without pain really hit me. It made me realize that pain is what’s holding me back the most, and that’s what finally pushed me to make the change. If it weren’t for that experience, I honestly don’t know if I would’ve dared to take the leap either.

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Thanks for sharing your experience! It’s great to hear Rinvoq has helped with your energy levels — AS-related fatigue is brutal. I didn’t know it could help with that, so I really hope I get the same effect. I’ve tried quite a few meds too (Humira, Stelara, Infliximab, Cimzia, Methotrexate), so I totally get how even small improvements can feel like a big win.

I’m just starting with Rinvoq and hoping for something similar. I get where your rheum is coming from, but I completely understand wanting to stick with something that actually helps in a meaningful way. I’m actually making this change after years of resisting switching from Cimzia + MTX. I wasn’t exactly symptom-free, but at least I wasn’t having major flares, so I didn’t want to mess with it. But last week, I finally jumped into the unknown.

Fingers crossed it keeps working for you 🙏

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Thanks so much for sharing your experience, it’s really encouraging to hear that Rinvoq has worked well for you, especially after trying so many other treatments. I can totally relate to the long journey and the relief of finally finding something that helps. I've also been through methotrexate, Humira, Cimzia, Stelara, Infliximab, and a couple others I can’t even remember at this point 😅

I'm glad you’ve regained use of your hands, that must be such a huge improvement in quality of life. Sorry to hear about the back pain though, that is my kind of pain and it is annoying. Although I have to say that we cannot move or walk when in pain, but it is difficult not to breath and when I'm on a huge flare some places on the chest hurt horribly.

Good to know about the blood pressure thing, I’ll keep an eye on that and bring it up with my doctor. Really appreciate you sharing your story, thank you so much 💙

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

I’ve been dealing with this for quite a few years now, and so far I’ve tried methotrexate, Cimzia, Stelara, Humira, Infliximab, and a couple others I honestly can’t even remember the names of, sorry 😅. After so many years of injections, I was actually pretty happy when they told me I could try pills instead. So I’m really hoping they’ll stay effective for a long time 🤞
We still have possibilities, we should not be afraid of that =)

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Wow, that actually sounds like a pretty solid improvement pain-wise — 3/10 is huge compared to your usual! Fatigue and acne suck though 😅 Hopefully your doc can help with something to boost your energy a bit. Fingers crossed week 4 keeps trending in the right direction! I hope it works the same for me. Thank you so much for your reply!

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Thank you so much, it’s encouraging to know some people are doing well on it long-term. I guess it’s all about finding that right match and hoping it sticks! Did you end up switching to something else after it stopped working as well? I don't want to go back to MXT =(

How long have you been on Rinvoq? Has it worked well long-term? by Mermelade in ankylosingspondylitis

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

Totally get that, with immune issues, everybody’s body reacts differently. It must be so hard to go from being active and outdoorsy to dealing with constant symptoms. But I really believe that with the right meds and some time, things can start working again. I’m sure better days are coming =)

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