u/ilikerustyspooonz

Image 1 — Fostering this mama and her 2 week old bb’s who were rescued from a hoarding situation. They don’t have names yet!
Image 2 — Fostering this mama and her 2 week old bb’s who were rescued from a hoarding situation. They don’t have names yet!
Image 3 — Fostering this mama and her 2 week old bb’s who were rescued from a hoarding situation. They don’t have names yet!
Image 4 — Fostering this mama and her 2 week old bb’s who were rescued from a hoarding situation. They don’t have names yet!
Image 5 — Fostering this mama and her 2 week old bb’s who were rescued from a hoarding situation. They don’t have names yet!

Fostering this mama and her 2 week old bb’s who were rescued from a hoarding situation. They don’t have names yet!

u/ilikerustyspooonz — 1 day ago
▲ 12 r/AskDocs

Am I truly too young to see a pain management doctor?

34 almost 35 year old female. 200lbs

Diagnosed with endometriosis, EDs, POTS, and MCAS. Psych diagnoses: ADHD, GAD, depression, PTSD, OCD.

I do have the MTHFR gene if relevant.

Current meds: bupropion 150mg, prozac 20mg, Adderall 30mg XR, clonazepam .5mg as needed, Pepcid, Zyrtec.

I have been in chronic pain since I was a child. Ever since I can remember I’ve been getting migraines, widespread body pain and muscle aches. Was always called “just double jointed” my entire childhood and adolescence. Got a HEDs diagnosis not too long ago. Everything made so much more sense.

My endometriosis causes me to have the most intense pain not only in my pelvis but throughout my body. I also have a chocolate cyst they are monitoring at the moment.

Every day for the last year, I’ve felt like something new hurts. I can hardly lift myself out of bed at times due to the severe pain I get in my back. There have been times I haven’t been able to walk at ALL even with the help of my boyfriend.

I have a chronic cough (8+ months) that leaves me to constantly be in pain in my rib area. When my MCAS is in a bad flare, all of my chronic pain issues intensify. 😭😭

I truly feel like I have no quality of life. I can hardly function majority of the time and it’s greatly affecting me as a mother especially. I have spoken to my primary care doctor about it, and she told me I am “too young to see a pain management doctor” so she won’t send a referral in for me. She also says they do not prescribe narcotics so she can’t send anything in for me either. She told me to continue to take ibuprofen and Tylenol. I have tried to explain to her that NSAIDS are a big trigger for my MCAS and that Tylenol doesn’t touch the type of pain I’m in.

They’ve had me try Tylenol, ibuprofen, meloxicam, naproxen, lidocaine patches, warm baths, warm/cold compress, exercise, stretching, supplements…none of that has helped even the slightest.

I have had to go to the emergency room a few times due to my pain and these are the meds they have tried:
-hydrocodone 5mg / wasn’t very effective
-codeine / wasn’t effective
-IV morphine 4mg wasn’t effective but 8mg was *highly* effective
-oxycodone 5mg / very effective especially for endometriosis flareup

I am currently in a bad flareup at the moment and it’s my hips, knees and back that are bothering me the most. I haven’t been able to do basic housework like do the dishes or vacuum because of the pain :( I would hate to go to the ER just to be able to get proper pain medication…but what else can I even do?

Am I truly too young to see a doctor for pain management or should I find a new PCP? My insurance requires a referral. I can’t imagine how much worse this will all be in 5-10 years if I can’t get control of it now. I’m in tears because this has been a lifelong battle and I just want relief so I can function without being treated like a drug seeker.

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u/ilikerustyspooonz — 3 days ago
▲ 33 r/Hounds

Help with foster dog!

Hi! I am fostering a 4 year old hound mix! I believe he is mixed with Rhodesian Ridgeback?

He’s doing a great job so far! But he has severe separation anxiety, so if he is alone he barks non stop. I am a stay at home mom so I’m pretty much never gone, but I would still like to help him with this because apparently he can become destructive. Even if I close the bathroom door, he comes up to it and barks for me and scratches at the door 😂 he is doing amazingly with my 5 year old and my 16 month old. Hes so sweet and cuddly!

Should I try and get a crate for him? How can I help introduce him to our cat in the best way for both of them? I understand that he needs lots of exercise and activity daily so I plan on taking him to the dog park and the beach, etc - but is there anything else I should know about his breed?! He will randomly walk up to me and start barking at me, but I have no idea what he is trying to tell me!!

I’ve never fostered before so I would appreciate any advice!

u/ilikerustyspooonz — 4 days ago
▲ 59 r/MCAS

MCAS & benzodiazepines

Hi! I am newly diagnosed and I’m in that stage where I’m putting my life’s puzzle pieces together and realizing how MCAS has actually been affecting me for my whole life. 😭

I’ve been on psych meds for my mental health since I was 18. I’m 34 now. It has seemed like not a single medication ever works for me (now I’m realizing it’s all probably histamine related) but the one medication that has ALWAYS helped me the most - is a benzodiazepine.

I’ve tried SSRI’s, SSNI’s, mood stabilizers, antipsychotics, you name it. And nothing seems to help my overall mental (and even physical) health as much as benzos.

Xanax, Klonopin, and Ativan all seem to be the only meds that ever make me feel well. I can easily stop taking them and don’t have a dependency on them or anything, but I have always wondered why nothing else helps and now I’m curious if it’s an MCAS thing?!

When I take a benzo, my skin is better, I’m less itchy and inflamed, my mood is better, my body isn’t in fight or flight mode, my HR is normal, it helps my appetite, even seems to help my adhd?!

I’m super curious on what everyone’s thoughts are?!

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u/ilikerustyspooonz — 4 days ago

Anyone else experiencing this with their most recent script from Elite labs?! 😳

EVERYtime I pick up my IR 10mg addy, it’s Elite manufacturer and it always sucks and feels like I didn’t take anything.

Well, I picked up my script for the month yesterday and took ONE 10mg pill and I was literally awake until 3am. My pupils were H U G E you would have thought I had taken Molly or did ❄️. I looked insane.

I was running around my house cleaning every tiny little crevice. It *actually* felt like the med was working for once but it did NOT feel like a 10mg tablet. It felt so intense as if I just took 60mg or higher. I was sweating BULLETS even my boyfriend noticed.

Today, took the same exact dose and I literally feel like I didn’t take anything. Like I could go to sleep for the rest of the day.

What the fuck is happening anymore lol

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u/ilikerustyspooonz — 5 days ago

I developed DRESS syndrome 5 years after starting lamictal 🥲

It’s been an absolute horrific month. I’ve been so, so sick and itchy and uncomfortable and in pain 😭 look how swollen my lymph nodes are in my armpit!! I’m so happy to finally know what’s been going on with my body though.

I’ve been covered in a severe rash with the most unbearable itching I’ve ever experienced, having abdomen pain, a horrible cough…they put me on amoxicillin at first (last month) which my psych thinks triggered everything with my lamictal. All my tattoos were risen and would start bleeding - it was crazy.

I’ve been to the ER 5 times this month and not a single person ever thought of this - even with my eosinophil levels being sky high. Thankfully I posted on askdocs and quite a few people mentioned it and it was like a lightbulb went off. I called my psych immediately

So my psych calls back and has me cold turkey it. I was on 150mg. I’m SO worried I’m going to experience bad withdrawal symptoms or that mentally I’m going to become unhinged lol. But my psych and pharmacist both told me I won’t have any type of withdrawal symptoms at all so fingers crossed

Has anyone had to stop lamictal and did you feel better or worse in terms of mental health? How was it stopping it?

u/ilikerustyspooonz — 7 days ago
▲ 407 r/AskDocs

35 female - 200lbs - history of endometriosis, long covid, allergic to dust mites, cats, dogs and oysters lol.

This will probably be a SO long but I’ll try and sum it up as best as I can!

Last night, I had two doctors in the ER arguing in front of me about whether or not I should be admitted to the hospital.

I’ve had an ongoing cough since January that has gone from a dry cough, to now a productive cough. A little over a month ago, I randomly noticed a rash appearing on my left breast. I currently breastfeed my son one time before he goes to bed, so at first I thought maybe I was developing mastitis. Breast cancer runs in my family so when the rash began to get worse and I noticed a lymph node in my left armpit was super swollen, I got really scared and called my PCP.

My PCP was very concerned but since it was the weekend she couldn’t see me so she advised me to go to the ER to be safe. At the ER (Mayo Clinic) I had the most lovely doctors who pretty much immediately ran a bunch of tests and did an ultrasound. The ultrasound didn’t show any obvious masses, but there were a few swollen lymph nodes in my left armpit. They took photos of the rash and did a thorough exam, and sent in a referral for me to get a mammogram and additional imaging. They had no clue what was going on but decided to treat it as mastitis to see if antibiotics helped. The put me amoxicillin to take for 10 days.

The rash rapidly started to erupt to my other breast and then to my arms, stomach, lower legs, inner thighs. (I will post lots of photos in comments of rash and labs) - it had been the itchiest most unbearable rash I have ever had in my life. I tried using Benadryl and it didn’t help. I tried hydrocortisone cream but it irritated it more. It became so severe that I went to see my PCP and tried calling the dermatologist but neither one could see me for two months, so my PCP put me on Keflex and a steroid pack.

Within two days, the rash became so bad that it was causing pain at this point. My skin began to blister and bleed. My cough got worse. I began to experience severe pain in my lower right abdomen and upper pelvis. Returned to Mayo.

The doctor I saw during this visit didn’t run any tests or anything but he said it was most likely a reaction to the keflex, so he decided to have me take doxycycline instead. He also prescribed me hydroxyzine (it did not help whatsoever).

Fast forward a week or so and my symptoms were so bad that again I called my PCP and she told me to return to Mayo. During this visit, they did labs, an xray, blood cultures, urinalysis and urine culture, and then a CT. Xray looked totally normal but doctor said the CT scan showed bronchitis (or some other airway disease) - and that I had a nodule on the bottom of my right lung. It also showed that I had a small kidney stone. My urinalysis showed elevated RBC. This doctor wanted to admit me to the hospital but it was already 6am and I had to get back home since I didn’t have childcare for my kids.

They gave me hydrocodone cough syrup for my cough (didn’t help) and gave me 2 IV antibiotics before discharging me. told me that if I didn’t improve to immediately go back.

Fast forward and you guessed it I was right back at Mayo. My cough is out of control, abdominal/pelvic pain was unbearable, and my rash somehow got even WORSE and my left arm began to become very inflamed and red and hot to the touch. It felt and looked like I may have had fluid buildup. The rash spread to my neck, back, and chest. It looked different too. The doctor I saw barely assessed my rash. He only looked at my forearms. He did bloodwork and next thing I know a nurse was coming in with discharge papers.

I was genuinely so confused so I asked her about it and she was insanely rude to me and made me feel annoying for even being there. She kept repeating “well this is an EMERGENCY room”. She asked me if I just wanted her to go get the doctor and I said yes please. When he returned, he told me that all of my labs looked completely normal and that it was most likely just an allergic reaction to something and that he could not do anything for me so he referred me to a dermatologist and allergist. I explained to him how I already had a referral and have been trying to get an appt with them for weeks now with no luck. He also said my cough was probably allergy related too and that my abdomen pain was “just my endometriosis” (lol).

He told me I should stop all of my medicines INCLUDING my psych meds and to stop using any products at all. (I am absolutely not going to cold turkey my psych meds) I asked him if he could atleast help me with pain relief and he shrugs and said “sure”. I got a notification on the Mayo Clinic portal that said I could view my labs so I went and checked them out and a couple of them were abnormal. My CBC w/ differential showed significant elevation of Eosinophils % and Eosinophils. I noticed that I had an updated lab from the visit before that showed an abnormal urine culture with enterococcus and abnormal usual flora. When he returned I asked him about these and he said they were just allergy related and sent me on my way.

I started bawling my eyes out 🥲 I told him I was just really frustrated and truly cannot go any longer suffering like this. I asked if there was any way I could speak to the doctor I saw during the visit before, so he had the nurse go and check if he was even working. Next thing I know, that doctor was walking into the room along with the current doctor I was just talking to.

It escalated so fast and the next thing I know they are literally both arguing with each other about whether I should be admitted to the hospital. The one I was seeing that night kept saying “this is an emergency department and she’s clearly fine to go home and wait to see a derm and allergist” he also kept repeating that my insurance wasn’t accepted there and that there wasn’t a case manager on shift to talk about it with. The other doctor was advocating for me SO much and told him that he should have seen in my health chart that he wanted me to be admitted and to take me seriously. I was actually shook and couldn’t believe what was happening but ultimately the current doctor said it was his call and that I needed to go home because there wasn’t anymore labs to be done and it’s “not like I was gonna get an MRI” (I had a literal wristband that said MRI on it so that was confusing lol) - he sent in a prescription for 5mg oxycodone (quantity of 5) and sent me on my way.

If you made it this far thank you so much for reading 😭 I called my dermatologist again today and asked to be put on a cancellation list. I’m waiting on a call from the allergist they sent a referral into. Tomorrow I plan on calling around to other dermatologists to try and get in asap. I’m genuinely in so much pain and discomfort that I haven’t been able to sleep much for weeks. It’s affecting me so much as a mother too. Does anyone have any ideas or thoughts on what could be happening? I know it’s a lot but I’m so desperate for answers 🥺

ETA I’ve had on and off fevers for the last 2 weeks

Update: woke up this morning with a migraine + vomiting 🥺 so over it

u/ilikerustyspooonz — 9 days ago