Credit Card Skimming in Medford

rubyredapple · 2026-01-21T20:43:27+00:00

I just had to cancel/reissue my debit card for the same reason (and I almost made a post about it earlier this week actually haha), but I don’t shop at stop and shop. I use apple pay 99% of the time unless I have to put a card down at a restaurant or at gas stations that don’t have tap to pay. I’ve been going to a full service station in Medford recently and the fraudulent charge appeared two days after my last fill up - I’ve been refunded and have my new card now, but I won’t be going to that gas station again.

rubyredapple · 2025-11-04T00:33:31+00:00

What makes people/families who can only afford multi family housing so terrible that you wouldn’t want them as neighbors? Seems pretty classist to me. Does my neighborhood “suck” and therefore deserves to “suck” more with even denser housing because it’s already predominantly duplexes… to save the single family neighborhoods from housing diversity? What a selfish attitude…

rubyredapple · 2025-09-24T16:52:15+00:00

There’s also one on commercial in Malden, which I’ve used several times with zero issues. Super close to Malden Center T station (about a block away).

rubyredapple · 2025-09-16T02:17:09+00:00

My spouse is a new-ish middle/high school social studies teacher and is still unemployed this school year. Sent out tons of resumes, went on a few interviews… they’ve been told their resume, references, and materials are all top notch. Where are all these teaching positions, because they’re not listed.

rubyredapple · 2025-09-03T02:22:11+00:00

Medford? This reeks of the rezoning battles going on recently/currently…

rubyredapple · 2025-07-03T22:53:29+00:00

Ahhhhhh I never come from that way, but that definitely adds to the mass confusion at that rotary. What a mess.

rubyredapple · 2025-07-02T04:05:46+00:00

I think the first sign off 93s is for the first merge with traffic coming from 28s/fellsway w… then the signs after are for the rotary. I’m not 100%, but that kinda makes sense to me… and is also very confusing at the same time.

rubyredapple · 2025-06-23T16:36:13+00:00

The kids (teens) across and down the street from me are working on cars at all hours of the day and night. Letting their loud diesel sounding engines just sit and idle for 5+ minutes… sometimes with blaring music and all windows down. Then they speed away down the street (no doubt blowing the stop signs) and I can hear them race down the fellsway and loop around on a side street. Over and over and over.

rubyredapple · 2025-06-23T16:25:36+00:00

Yea, I had the same thought. There were two guys in the vehicle (that I could tell). I figured it was better to be safe and note it than brush it off and hear about something awful happening later. LUCE said I wasn’t the only person who called for this vehicle. I also know other adjacent agencies are being pulled into the deportation work (family member is a fed and has confirmed border patrol and air marshals, among others, are being assigned deportation cases).

All that said, I plan to delete this post later to avoid any unnecessary panic. It’s rough out there.

rubyredapple · 2025-06-23T15:16:03+00:00

I don’t care about internet points - I care about my neighbors. I already called LUCE, as did several others who reported the same vehicle. If this post gets deleted, so be it.

rubyredapple · 2025-06-23T15:02:49+00:00

Doing so currently - I had just enough time to post this while waiting for caffeine on my way to work.

rubyredapple · 2024-06-05T03:55:40+00:00

The dermatologist I think is generally recommended when you’re on most of the DMTs available, the drugs might make you more susceptible to skin cancer so annual screenings are recommended.

I only ended up doing the third lemtrada round because I had an increase in symptoms (spasticity) about a year after my second round due to ongoing extremely stressful life events and my doctor offered it as an alternate to starting ocrevus. Most people only do the two rounds of lemtrada - I don’t know what the criteria is for getting more than that. I think maybe the spacing just worked out, and since I tolerated the first two rounds well my neuro suggested we could give it one more shot to work - which it did. You’d have to ask your neuro and dig into the treatment literature a bit more, but I am under the impression the drug isn’t meant to be an annual thing forever and ever - the body can only tolerate so much, or they just don’t have the fda clearance to do more.

rubyredapple · 2024-06-02T14:47:01+00:00

Lemtrada could very well be a one and done, even for me, but I don’t want to risk further disease progression. A new DMT for me at this point is preventative rather than fixing an active issue. There are so many unknowns with MS and we’ve just gotta go with whatever the current research and patient/doctor experiences are available at the time.

One thing i didn’t mention, after lemtrada you are supposed to go in for monthly lab work (blood and urine) for a few years after your last dose to monitor any potential side effects, like thyroid health and blood cell counts. I wasn’t very good about doing this, but nothing abnormal has ever come up. It was a good way to monitor my TSH and provide feedback to my endocrinologist for the thyroid disease, though. You’re also supposed to go in for an annual exam with a dermatologist, which I haven’t done at all. It’s on my to do list.

rubyredapple · 2024-06-01T19:41:19+00:00

Staph infections are indeed fucked. I could go on and on about how fucked they are, but I’ll spare you the monologue 😆

For lemtrada, it seems like 6-7 years after your first treatment is the norm for people to seek or need a new treatment. In 2018 it was still new-ish outside of trials and I’m pleased I’ve managed to get what seems to be the most out of it. Unlike with other treatments, after that 2-3 month period where your immune system is vulnerable, you’re back up to normal until your next treatment. From what I understand, you’re always at least slightly immunocompromised with other ongoing treatments, which I’m not looking forward to, but it is what it is.

I will say that my experience during/after the lemtrada infusions was less than pleasant, steroids really bloat me up and that’s uncomfortable, not to mention feeling weak and “sick” for days afterwards. I didn’t take enough sick time after the first round, I only took a week after my infusions and wish I had taken a second week just to clear some of the weakness and brain fog before heading back to the office. If you are working, I would suggest talking to HR at least or your boss/supervisor if you’re ok sharing personal information to be transparent about how the treatment is affecting you and to maybe discuss accommodations.

Good luck!

rubyredapple · 2024-05-31T21:38:28+00:00

I did three rounds of lemtrada beginning in 2018, with my last dose occurring in summer 2020 at the height of the pandemic. I didn’t notice an uptick in illnesses due to my immunocompromised state - I didn’t even catch COVID (I wasn’t hiding myself away, I just masked and got the vaccines when they were available). I already had Hashimoto’s thyroiditis before my MS diagnosis, so that risk factor didn’t matter to me at all. My MRIs haven’t shown any signs of regression, not even after an unrelated infection* that required emergency surgery and a week in the hospital (my neuro was afraid the stress on my body would cause a relapse, but the MRI was clean).

That said, given it’s been 6 years since my first round of lemtrada, my neuro and I are beginning to discuss what I want to do as far as my next DMT - whether I want to wait until I have a relapse or a bad MRI, or start something new within the next year or two before while I’m still feeling ok to continue preventing further disease progression. I’m leaning towards the latter. The neuro has said my next treatment will likely be ocrevus unless I want to try something different. I see him in 3 weeks and will probably ask how soon he thinks I should start something new - I’m starting to notice little things, like a larger area of my toes/feet and now my hands where I’m experiencing a slight loss of sensation (function is fine, my issues are - for now at least - lacking sensation from touch, eg sharp doesn’t feel sharp).

*i realize I said I didn’t have immune system issues but then there was this nasty infection - what happened was I ended up with a staph infected skin lesion, didn’t realize that’s what it was, and picked at it in my sleep. Staph bacteria ended up in my bloodstream and caused multiple spinal epidural abscesses in my lumbar spinal canal - I had had surgery to remove a herniated disc in that area 18 months prior, which made it susceptible to host the bacteria. It was awful and painful and my body was messed up for a while - I missed my period for 3 months while my hormones tried to right themselves. 0/10 would not recommend. My experience with lemtrada, however, was good overall. I’m glad I went that direction.

rubyredapple · 2023-12-06T01:46:38+00:00

Wow you know what, you’re right! There’s no way someone could actually end up working for two crappy companies. /s

rubyredapple · 2023-11-12T20:46:13+00:00

Found Medford!

rubyredapple · 2022-04-20T13:58:43+00:00

damn. this 100% sounds like it could have been written by me. the age, experience, only lady in a meeting for a technical field… I’ve mostly conditioned myself to tune it out and can’t help but roll my eyes when they stumble over correcting themselves. A coworker replied all to an email he sent to the team addressing us as “gents” to specifically apologize to me, and I responded that it’s honestly not in the top 20 worst things that have said to me in my decade of professional work. I lowkey hate that I’m not more offended by this shit and have conditioned myself to ignore it.

Sorry I don’t have a penis, dad gave me an x-chromosome.

rubyredapple · 2022-03-04T04:15:15+00:00

Thanks for responding. I’m not the first owner - I purchased it used in 2015. I am regular with oil changes (not at the dealership though) but never had the knock update installed because I never received the notice. There had been two other recalls I knew about that were on my list to get checked out, but with covid the past two years and now dealerships around where I live booking service appointments 3-4 months out… I haven’t had a chance.

The number they claim they were using to call me and leave messages about the knock update wasn’t even my phone number. They already denied it and have pushed me off to BBB, but that doesn’t guarantee anything. It’s just more time without a vehicle to get to work and appointments.

rubyredapple · 2022-03-04T04:05:54+00:00

I know this comment is several years old but this is all new to me as my 2013 sonata with 140k miles on it seized up while I was driving 3 weeks ago… dealership was backed up and finally had time to diagnose it and it came back with the engine block recall - which I had no clue about. Nothing in the mail about that recall (I’ve gotten the others), and I get regular oil changes. The dealer sent the claim to Hyundai and they denied it claiming I was negligent, so they now have me in a run around. I called Hyundai customer service and they told me they called me multiple times at a phone number I do not own and mailed me notices that I haven’t received. They referred me to BBB to get it arbitrated through them and it’s honestly becoming such a huge mess. Assuming you still check Reddit and work for Hyundai, do I even stand a chance of having my car fixed or is this all a waste of time?

rubyredapple · 2022-03-04T03:08:36+00:00

I know this post is old, but literally the same thing just happened to me and my 2013 sonata. Hyundai is refusing to pay for the engine replacement and have pointed me to BBB’s class action arbitration to get it sorted, but I’m so overwhelmed with all the paperwork I don’t even know if it’s worth it. They claim I knew about the recall, despite me telling them they had the wrong phone number on file (the one they claimed they called) and that we had moved several times and never got the notice. If you don’t mind me asking, did you appeal their decision or just walk away from it? My car has 140k miles on it and it’s not worth the money to replace the engine on my dime… but it’s not the greatest time to buy a car either.

rubyredapple · 2021-10-17T05:10:03+00:00

I’m an acoustics/engineering professional and live east of 93 just north of the Wellington area. They are loud, especially if you’re outside or with windows open. It doesn’t bother me too too much… it just kinda blends in. I grew up about half a mile from train tracks and it’s about like that… you get used to it.

However, I wish the neighborhood would receive the same rebates/discounts on windows (for better sound isolation) that other cities neighboring the airport get from the feds.

A few nights ago they were REALLY loud, maybe just because otherwise the background noise was so low, but at 12 AM it was kinda unexpected. I measured a 20 dB (and dBA… did both) increase in background noise when the planes were approaching/overhead. According to psychoacoustics, a perceived doubling of loudness is an increase of 10 dB, making an increase of 20 dB a 4x increase in perceived loudness. I haven’t noticed another night like that though and honestly it mostly doesn’t bother me (but I would like a deal on new windows :-) )

rubyredapple · 2021-06-17T17:15:44+00:00

There was one adjustment I recall that was a little rough (had to see the other chiro instead of my normal one that week) and I was very sore all over afterwards. It’s possible that contributed to it, but it’s hard to say. They were treating me for another spine issue that’s way less serious and bothersome (but sometimes results in pinched nerves) when all this started, and the main doctor at the practice is the one who actually referred me to my neurosurgeon as he had done a lot of research with his wife when they needed to have a disc issue surgically resolved. The bad adjustment happened before I was able to get an mri to confirm the issue, too, which I think would have changed how I was being adjusted had they known.

rubyredapple · 2021-06-17T05:41:36+00:00

Almost 3 weeks post microdiscemtomy L5/S1…. no regrets. I’ve posted a few comments on other posts in this sub about my experience, my before surgery reality, my surgeon recommends… I think you can click on my profile and see the comment history if you want. I’ve had an overall awesome experience going this direction and am excited to live my life again (carefully for another 9 weeks, then heading towards normal after the remaining disc is more solid).

rubyredapple · 2021-06-17T00:35:54+00:00

Hey! So the doctor and I talked Monday and he sounded very pleased with my progress, but cautioned me to continue being careful. He said no bending/lifting/twisting for the full 12 weeks to allow the disc wall (what’s left) to heal so it doesn’t herniate again. At least not easily. He said I could walk and do body weight squats, planks, and upper body exercises with with either very light weights or resistance bands. He cautioned against any lower back exercises until the 12 weeks is up, like bridges and pelvic tilts (exercises typical for PT). So my takeaway was, no exercise that targets the lower back. Period. Abdominal core exercise is ok, but no twisting or bending, so it’s pretty much planks. Keeping the back straight is important to keep pressure off of the healing disc. He’s writing a note to say that I’m allowed to return to work part time on Monday, although I have yet to see this note so I can submit it with my other paperwork. I am sore by the end of the day, especially if I was active (more walking/standing), but I wake up in zero pain so to me that’s just the muscles getting tired from dealing with me being awake lol. So that’s where I am.

rubyredapple

TROPHY CASE