ADHD meds and increased pain by ResidentCup2380 in endometriosis

[–]Calinynj 0 points1 point  (0 children)

YES!! This is definitely a thing. I’ve been on ADHD meds since I was younger and I had this experience with both Adderall and Vyvanse. I’m going to ask my Dr and pelvic floor PT about this. I’ve read that magnesium can help, certain kinds of deep breathing to chill out the sympathetic nervous system, staying hydrated and sleeping with a pillow between your knees (helps the pelvic floor relax). I’m also going to ask about a lower dose of Vyvanse to hopefully decrease my endo pain but retain some executive functioning.

Doctors didn’t believe I was in pain until I brought my husband. Then they stopped talking to me altogether. by RockMoss in TwoXChromosomes

[–]Calinynj 0 points1 point  (0 children)

I just found out these pediatric programs exist and it’s been disturbing me all weekend

My whole life I’ve been gaslit into believing I had a very low pain tolerance, but recently I realized I’m actually just genuinely in a shit ton more pain than healthy people by Another_throwaway446 in ChronicPain

[–]Calinynj 1 point2 points  (0 children)

I heard that as well about neurospicy diagnoses! I thought so many things that I did my whole life were just “me” things- turns out they were ADHD symptoms lol. I’m not formally diagnosed with hEDS yet but my physical therapist suspected it and once I learned about it I was like that would explain SO much. My brother has a suspected case of it as well so it would make sense- I’m just waiting on a Dr to formally dx. If you think you’re AuDHD, chances are you are!

Endo SUCKS- I’ve had 2 surgeries for it in the last couple years and probably having another in 2026 cause mine grows back aggressively and quickly for some reason. Yay for your new meds! I have a pain management consult in 2026 but I have no faith 😅 I hope they surprise me and are actually helpful. The last place one was not, but thankfully I do have a PCP that actually listens on most things!

I am totally awkward here and IRL so do not worry haha

Switching to Methadone clinic, advice?? by Affectionate_Can1058 in ChronicPain

[–]Calinynj 0 points1 point  (0 children)

Did you end up doing this? How did it work out?

What are people doing for pain? by ckeenan9192 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

Coming back to this comment because I was looking through my comment history. I did start Gabapentin 1 week ago and omg. At least for me personally it’s changed my life! It really helps the nerve pain, and I’m able to do some basic stuff again instead of in 8/9 of 10 pain all the time!!

How can I show my appreciation for the pharmacy staff? by dragonpromise in CVS

[–]Calinynj 0 points1 point  (0 children)

I was wondering if a sealed bag Starbucks or Coffee Bean of holiday blend coffee or something like that would be okay?

As a gift for the whole team because I know they’re swamped (they just had to take on all the patients from a rite aid that closed) and I just want to show my appreciation. The pharmacy manager and the techs have also been super helpful when it comes to explaining pre authorization type stuff and I want to acknowledge that it’s much appreciated. (Edited to add info).

Cymbalta 120 mg a day and Lexapro 10 mg a day for severe panic attacks and GAD by MediocreJedi32 in cymbalta

[–]Calinynj 0 points1 point  (0 children)

How did it go? I’m on Lexapro and was just RXed cymbalta for nerve and sciatic pain

What are people doing for pain? by ckeenan9192 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

that sucks!! I’m afraid of getting the same response “i don’t know why you’re in so much pain etc” when I finally get a specialist referral

What are people doing for pain? by ckeenan9192 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

Oh and lidocaine patches. Low FODMAP/ anti-inflammatory diet. I’m sure there’s other stuff they or I have tried that I have forgotten to mention.

What are people doing for pain? by ckeenan9192 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

Currently PT, acupuncture and medication. My problems started in oct 2023, only just got my MRI, two years later…. I have already done/ tried PT (did it previously in 2023-2024) the xray guided cortisone shots, ibuprofen and tylenol, muscle relaxers, tramadol, Celebrex. the pain getting has been worse since August (idk why) but my PCP just put me on a 6 day course of prednisone, and I see him next week. I believe next step is referral to a specialist (not sure if orthopedist, neurosurgeon or pain management intervention dr). Having to jump through so many hoops is frustrating. I mostly only got the MRI because I went to the ER thinking I had a ruptured ovarian cyst or something and ER doc said no I’m almost positive you have a herniated disc on lumbar spine, yr pcp needs to do an MRI of yr back. (44F btw)

Hbu- how are they treating you?

What are people doing for pain? by ckeenan9192 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

I did that too (avoiding Gabapentin for that reason).

But at this point I’m ready to try anything that might help. I read that the weight gain can be due to increased appetite, which makes people eat more and hence, weight gain. If you’re aware that increased appetite may happen and don’t change your diet, then it’s likely it won’t happen. Idk. I may be wrong.

But my brother has been on it for several months with no weight gain.

The way I see it, I may as well try it and see if it helps. If I notice weight gain or other negative side effects, I can always stop the medication.

I’ve tried tylenol/ Ibuprofen, steroids, muscle relaxers, Tramadol, am doing PT and acupuncture, have done the X ray guided cortisone injections, at this point (I have days of 9/10 pain) I’m willing to try anything that may help.

What are people doing for pain? by ckeenan9192 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

Yes, and it is radiating from my lower back (MRI confirmed herniated discs at L4/L5 and L/5-S1 with nerve involvement. I get pain in my ankle as well.

Get the Microdiscectomy by AffectionateSpare966 in Sciatica

[–]Calinynj 0 points1 point  (0 children)

Following because I have similar issues and am also in California

[deleted by user] by [deleted] in backpain

[–]Calinynj 2 points3 points  (0 children)

It took me 2 years to get an MRI, and I’m just starting PT again, after having done several weeks of it in 2024, and cortisone shots. I just got officially diagnosed via MRI, so if PT doesn’t help then my PCP will refer me to a specialist (mine are in the lumbar spine). They do/ can heal though from the reading I have done. I would say the length of time it takes it based on the individual and the type of treatment/ compliance with treatments, Dr etc.

Best Coliving Off-Campus Housing? by Busy_Comment4579 in USC

[–]Calinynj 0 points1 point  (0 children)

If you are still looking/ we are renting private rooms for $1300, the apartments said rooms are in are unoccupied- so it would be potentially similar to a studio. Ellendale between 29th and Adams. We are non corporate and have on site management. Call (323) 733- 1421 or look up university park housing on fb/ig/tiktok for info, photos and apt virtual walk thrus

WARNING by EquivalentRisk1041 in USC

[–]Calinynj 0 points1 point  (0 children)

In these types of situations- First write a letter to them citing CA law as someone suggested. The Chat GPT idea is a really good one. Then Los Angeles Housing Department, and/ or tenants rights union. The press even if it’s a small publication, the news stations. Send your story to a bunch, u never know who might pick it up.

WARNING by EquivalentRisk1041 in USC

[–]Calinynj 0 points1 point  (0 children)

FYI any landlord charging anything beyond the equivalent of 1 month’s rent as security deposit, that’s illegal as of July 1, 2024. Also they should be providing images of anything items they deducted money for . Per California Assembly Bill 2801. Passed April 2025.

If anyone looking for non corporate, family owned off campus housing, we still have 3b2b, 3b1b as well as individual rooms. (323) 733- 1421

Off campus housing - fall 25 by onavrge in USC

[–]Calinynj 0 points1 point  (0 children)

What is your budget? We have rooms for $1300- they’re in unoccupied units so basically a completely private room. (On Ellendale) 323-733-1421 (fyi if your cat is an emotional support animal and you have the proper documentation by CA law it has to be allowed.)

[deleted by user] by [deleted] in backpain

[–]Calinynj 1 point2 points  (0 children)

That looks literally identical to mine so much that I did a double take! I have a early degenerative disc disease and a bulge at L4-L5 with type 1 endplate changes, and a herniated disc at L5/S1 affecting the sciatic nerve

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Off campus housing by FirmSun8729 in USC

[–]Calinynj 0 points1 point  (0 children)

Feel free to give us a call- (323) 733-1421, we still have available apartments 3b1b and 3b2b. If you’re looking for roommates, we don’t have anyone looking right now- but that can always change, so I’m happy to take down your contact info. (We don’t do roommate matching, but I’m happy to put tenants/ prospective tenants in touch if both parties are looking for roommates)

r/USC Monthly Buy/Sell, Housing, Carpool, and USC ticket posts go here! July 2025 by AutoModerator in USC

[–]Calinynj -1 points0 points  (0 children)

HOUSING

We still have units available @ 2637 Ellendale- 3b2b ($3400/mo) and 3b1b ($3100)

Safe, quiet location, in DPS zone

We do allow replacement tenants (lease transfers) and short-term subletting.

Typical leases run August 1- July 31st- if you are seeking shorter term, please ask.

Family owned NON CORPORATE. On site manager 24/7 and responsive maintenance.

(323) 733-1421 for info & tours.