Help! How much would you guys pay?
2025.01.24 05:51 Smoreheat Help! How much would you guys pay?
Really been wanting these for a while and can’t justify paying 500 for my self but found this use pair. Just wanna know how much would you guys pay. Wanna make sure I’m not over paying which is $200
submitted by Smoreheat to Newbalance [link] [comments]
2025.01.24 05:51 froderick Cunk & The Rise of Anti-Intellectualism
 | submitted by froderick to Asmongold [link] [comments] |
2025.01.24 05:51 Responsible_Pin_2272 flatbox rev3 question
For anyone that's built a rev3 do I need header pins to solder the brook pcb onto the flatbox pcb, ordered the parts but was looking at it and was a little confused how I should actually solder the board on it. It doesnt mention anything about it in the documentation but this comment is there " (the plastic base of the pin header can't go between the Brook board and the PCB)." so was wondering.
submitted by Responsible_Pin_2272 to fightsticks [link] [comments]
2025.01.24 05:51 ivan3295 I'm 29 years old, male. Dealing with intense throbbing/pulsing of my veins and arteries in my upper back, neck, and head and light headedness and lack of equilibrium that gets worse when I bend, twist, or arch my spine or neck, tachy, and progressive muscle weakness. Need medical advice.
Fair warning , this is a really long post because my medical history and symptoms have lasted years and progressed instead of stayed stable.
The tachycardia also comes with fluctuations in blood pressure, both going up and down.
I can have sudden Vital Spikes out of nowhere and they are always worse at the onset and can take a whole day (or falling asleep) to go back down, or can last as short as half an hour.
I've had my heart rate spike into the mid hundreds with my blood pressure as high as 164/135 at the same time, with the most intense pulsing being below my chest (top of belly visibly jumps), upper back, and the back of my neck and head.
While less worrisome, I can also have vital drops. My heart rate can drop for example from the 90's to the 70's or 60's while I'm standing and when that happens I suddenly feel my body physically get heavier.
While my spikes aren't very often, my vitals do fluctuate alot throughout the day and I can have a high blood pressure rone day and a normal the next (with throbbing/pulsing being more intense in my head and neck at lower vitals)
Doctors have been telling me for years (as it's gotten worse) that it's anxiety related (with no proof or history on their end to back up an anxiety claim,they just assume based on lack of medical evidence for a definitive diagnosis, but don't even bother asking me about stressers or if I have any anxiety and would rather tell me "you're just anxious and don't KNOW you are").
If anything other than randomly, anything I do physically can also cause me long term tachy for some reason. I could eat a bite of food and have a spike before it even reaches my stomach (used to happen frequently), or eat a huge meal and not get any spike, however liquids seem to not trigger it. I can also have a spike, or get really lightheaded and lose my sense of balance and equilibrium when I bend or twist my spine or neck (nothing major. Think looking down at your phone or laying face down and arching your back slightly)
From 2022-2023 the tachy lasted almost all day, and got so worse over time that I went from 286 pounds (before getting covid. I had my symptoms before that but nothing compared to after covid) to 197 pounds by May of the next year.
(I'm now 286 again because they pushed me to take psych meds and the original ones they had me on made me gain all the weight back that I lost in 6 months, so I had them changed)
I also went from getting 130bpm spikes in January 2022 to getting up to 180's by that July (highest heart rate I ever had. Blood pressure would also spike and fluctuate the same way heart rate would)
The weight loss seemed to affect my muscles and circulation because I didn't start having balance issues, equilibrium issues, or muscle twitches (they feel like vascular spasms/twitches) and muscle thinning/weakening until after a few months when I lost 20-30 pounds.
Sensory wise both hot and cold feel very dull/not clear to me unless I'm directly touching something or experience a drastic temperature change and many times I won't realize I'm cold until my body starts shivering or that I'm hot until I start feeling pain (if something's too hot) or sweating.
My vision started getting worse (not too bad though) and I developed tinnitus (first it was pulsatile tinnitus, then it became ringing)
I went from being able to walk every day for 30 minutes or more (with my muscles only getting thinner over time), to needing a walker, not being able to drive (due to sudden random losses of equilibrium where I see and feel everything moving especially internally) and then eventually needing having to stay at home almost 24/7.
Whenever I get tachy now, I get muscle pain and soreness all over my body that last for days. My amino acid tests ordered by my neurologist from cleveland clinic once showed I had quite a few of them low, but the recommendation was just to eat more protein....which made me laugh because I eat protein with every meal so suggesting I had a lack of protein intake was laughable, if anything I need more veggies and I've been worried I can't process protein properly anymore due to the steady muscle weakening for years and low testosterone for my age (180-330)
I also randomly get intense burning where my thyroid is.
It feels like my body lost it's sense of equilibrium/homeostasis and over reacts too wildly to simple stimuli like neck movements or eating, or the opposite, reacts barely at all (think trying to run or physically exert yourself but your heart rate won't go up to compensate so you're almost stuck in cruise control physically)
I've had every test imaginable in the past 3 years.
Vascular tests with a vascular surgeon came out normal with a sinus heart rhythm.
Holtor monitors with cardiologist show the heart rate spikes but no arrhythmias or irregular electrical activity so it basically looks to them like I'm exercising on the monitor when im reality im just sitting there getting spike doing nothing or doing something small like a sudden movement or eating.
EMG, NCV, and EEG studies with two different neurologist are normal (couldn't get a muscle biopsy because they won't give you one if the above tests are negative)
I only had one time where my EKG suggested a possible myocardial infarction during a vital spike that got me in the er but they dismissed it because my troponin and CK levels are always normal in my blood and my rhythm is always normal.
Colonoscopy and endoscopy normal.
Negative for rheumatism and arthritis .
Negative for infectious diseases.
Negative for diseases in the eye ( I started seeing colore spots and electric sparks sometimes and even temporarily had visual snow when my vitals were at there worst in 2022)
Negative for aids or HIV.
Negative for muscle wasting (CK levels in the the blood are normal) BUT highish ck levels once in my urine (they go by blood and tend to ignore urine)
MRI of brain shows no lesions.
MRI of spine shows only slightly protruding discs in my neck with no stenosis, and a possibly congenital narrowing of my lumbar spine at the bottom.
Ct angiograms were MOSTLY normal (more on that when I post some of my tests below) and echocardiogram only showed VERY MINOR regurgitation in three of my four heart valves (aortic was fine)
Hormone tests were mostly normal except for testorone and prolactin (more on the prolactin below)
Blood tests are always normal with no signs of cancer, infection, etc.
As of today I can barely do much besides sit and watch TV and can't lay the back of my neck, head, or upper back against the couch or on my bed without getting really lightheaded, losing sense of equilibrium, and my upper back, neck, and back of head having a really strong pulse (even at normal heart rate and blood pressure). I haven't worked in three years because of the intensity and unpredictable nature of my sudden spikes, while my body itself has gotten physically weaker, muscles progressively thinner, and balance/equilibrium worse to the point where I can step on the ground and feel my foot "sink" instead of The ground pushing it back up, even though I know my foot is on the ground, my body doesn't seem to be sending the signals to my brain telling it "there's a floor here"
My ability to feel any type of pleasure is almost entirely gone as well. I don't mean this in a psychological detachment way where it goes away if I'm on psych meds, I mean quite literally my pleasure response stopped working. I can eat and detect WHAT I'm tasting or smelling but my body won't send pleasure OR disgust responses.
I feel no sense of pleasure activation from getting something like an arm rub, smells, and barely feel any pleasure in my penis area. If anything, it's almost like the nerve controlling the sense of pleasure was cut off almost entirely so if I have an erection, the hardness and throbbing actually cause me pain and the pleasure is no longer intense enough to overcome it.
As of right now my upper back (so not the chest but BEHIND the heart), back of neck, and the back and middle of my head are pulsing hard all day, worse at "healthy" heart rate and blood pressure levels (think the pulse you feel in your arm when a blood pressure cuff is loosening, but spread out to my whole neck, upper back, and head. Like feel all the veins pulsing individually at once instead of a vein throbbing in one spot)
This only goes away when I raise my heart rate but comes back at rest.
When I bend or stretch those areas even just to look at my phone for too long the pulsing gets worse.
All these symptoms and more are overwhelming for me but even more so for doctors because they say they can't pinpoint a diagnosis on such a broad range of symptoms, but the thing is it was originally few (like the tachycardia), but eventually made other things worse (muscles, balance, sensory) over time as the weight, muscle, and muscle control got worse.
💥Concerning my positive Tests💥
As for the tests that did show something, they were either seen as not a big deal or 'inconconclusive isolated incidents" due to lack of a consistent pattern.
Autonomic and tilt table tests showed possible signs of pots, hyper adrenergic tumors, etc. but nothing definitive for a diagnosis or Autonomic disorder only acknowledgement that it could be cause of having contracting covi, but my symptoms didn't START with covid, they only got worse.
Results stated:
"The cardiovagal, cardiovascular adrenergic and sudomotor adrenergic/cholinergic responses were normal There is no compelling evidence for autonomic neuropathies. However there was evidence for hyperadrenergic orthostatic tachycardia. These may be observed in those who carry the conglomerate of symptoms suggesting a POTS syndrome and other conditions such as dehydration, tachycardia, deconditioning, high adrenergic tone such as anxiety and abdominal catecholamine producing tumors and others, hypermobility syndrome and in association with COVID-19."
However I was advised to follow up instead with a different doctor by the neurologist who conducted the above tests because of my CT angiogram results and him saying I don't have anything neurological
He also ordered an amino acid blood test.
Many of my amino acids were low but I was told by a cardiologist that was not a major issue even though I'm concerned my bodies having trouble digesting protein properly due to the muscle loss over the years that doesn't respond to exercise or protein intake and the low amino acids even though I'm definitely eating protein (was on antibiotics recently and had to stop taking them because I woke up feeling like throwing up and pooping at the same time and my poop came out like sludge/melted chocolate, which I was told by a relative was a sign of the body not digesting fat. I stopped the antibiotic and it went away.)
For the two years my fluctuating tachycardia and blood pressure were at their worst (2022-2023), my prolactin hormone levels were constantly going up, and did not drop back to normal until late 2023.
As for my throbbing pulse and weakness in upper body, at its worst I had to go to Cleveland clinic by ambulance due to extreme sudden heaviness in my entire body, And high heart rate and Struggling not to pass out. I was told it was NOT a stroke or heart attack, but my CT with contrast scan of my neck and head reported as follows:
"Head and Neck CTA
History: Transient ischemic attack (TIA)
Technique: Multiple thin section axial images through the head and neck were obtained with IV contrast. Multiplanar 3D MIP images were performed.
Intravenous Contrast: Yes,100cc -- Omnipaque 350
Comparison: None
CT Radiation dose: Integrated Dose-length product (DLP) for this visit = 1408 mGy*cm. CT Dose Reduction Employed: No dose reduction techniques were required
Result:
Head:
The intracranial vasculature appears diffusely narrowed, irregular and beaded. Severe narrowing in the nondominant right vertebral artery, left P2 PCA and the bilateral anterior M2 division of MCAs is noted. There is no ectasia or aneurysmal dilatation. There is no dissection identified. The left vertebral artery is dominant. The anterior communicating artery is not visualized. The left posterior communicating artery is not visualized. The right posterior communicating artery is patent.
Neck:
There is no significant ectasia or aneurysmal dilatation visualized on the current study.
Carotid Stenosis: Right Common: No significant stenosis. Right Internal Carotid Plaque: No significant plaque formation. Right Internal Carotid Stenosis (% by NASCET Criteria): 0
Left Common: No significant stenosis. Left Internal Carotid Plaque: No significant plaque formation. Left Internal Carotid Stenosis (% by NASCET Criteria): 0
Cervical Vertebral Arteries: Patency: Bilateral Dominance: Left
Impression:
Diffuse beading and small caliber of the intracranial vasculature suggestive of reversible vasoconstriction or vasculitis. Comparison with a prior scan may be helpful. Correlate clinically."
The arteries listed are the same arteries I feel throbbing in my back, neck ,and head, and where my symptoms get worse if I bend my neck or spine or press them against something when I sit back or lay face up.
Doctors did not continue pursuing this issue because when I went to the ER again a week later at a different hospital (I moved and can no longer get to Cleveland clinic) my brain MRI and MRA were clear showing none of the narrowing from the week before, but my telemetry records while admitted into that second hospital showed my heart rate jumping up and down and averaging at 108bpm or so but reaching much higher (and lower) constantly. Was not a stable heart rate that stayed at one beat and could jump up and down from 100's to 60's
My tsh levels have always been normal EXCEPT for one time where it shot up to 9.4 (normal range for quest labs was about up to 4.5)
Finally, out of the four times I've tested my blood for ANA testing, I was positive three times (however a low ratio of 1:80) and my myositis blood panel was negative and my rheumatologist advised to try the psych meds route for a bit (because of how stressed out my family looked pushing the psych route) and if things didn't improve I could go back and do more tests.
To summarize, fast forward two years later, I no longer go to the ER regularly. No one will take me and I can no longer physically get there on my own since I can't drive or walk and do all my medical appointments virtually. I honestly don't even want to go because we doctors don't really care about caring for you if you aren't literally dying. My family gets angry at me or with me when I feel bad and treat me like my sudden (and observable on a monitor or test) vital spikes are self induced and will even leave the room, or like my muscle and balance issues are fake, and I've even had family members who have SEEN me fall on the floor or struggle to walk in the past ask me "why are you BEHAVING that way" as if my issues are just an anxiety induced cry for attention, This is partly due to medical ignorance and not knowing what's urgent or not and relying on doctors telling them it's all anxiety (or conversion disorder) vs. actually researching what's okay and what isn't. They're constantly pushing me to do things I can no longer physically do like exercise and treating me like I never did to begin with and like I made up having ever exercised at all . They call me stubborn for not listening to their "medical advice" and accusing me of "not wanting to get better" when I've actually done everything they AND doctors have suggested multiple times with no results(some er visits, specific specialists, pain meds, allergy meds, psych meds for two years and counting, all with no answer and no improvement in my constant physical symptoms.) and every time it's a different excuse. If I don't take meds I feel I don't need or that don't improve me in any way, they say 'I don't want to get better", if I take them and they don't help, they tell me I should ask for a higher dose.
I was diagnosed with conversion disorder due to lack of medical evidence for my symptoms, INSTEAD of getting an actual psych evaluation and seeing if my symptoms improved or not on meds or if there were any mental traumas that were triggering my symptoms (conversion disorder is not anxiety disorder. It's more linked to repressed trauma than anxiety. If the cause is anxiety, it would be psychosomatization). They just kept drugging me and even injected me to try to "calm me down" and treated me like I was better while I was limping to my bed.
I come from a family that is ignorant of medical knowledge and terminology, but even worse with psychological and psychiatric terminology. Many of them even had my diagnosis wrong for a year and thought I was diagnosed with an anxiety disorder instead of conversion disorder. Why? They didn't ask me. Apologies for the family vent. It's hard because due to my physical inability I'm now dependent on them to get serviced and go to doctor visits and being treated like I don't want to get better or like I'm faking my symptoms (even the vitals and muscle twitches and contractions) has been....horrible, to say the least.
It's honestly to the point where they can't hear me say I feel bad without getting angry and accusing me of being delusional or lacking boundaries when truth is I just want to get better and move somewhere with my wife as far away as possible, but can't die to physical limitations and needing the support system for resources with family.
While my tachycardia is no longer constant and the weight loss stopped, my heart rate and blood pressure still fluctuate randomly which feels horrible (weak one second, fine hours later, won't go up or down when needed, etc, )
My equilibrium and balance never came back and only get worse if I keep my neck or spine bent or press something against the back of my head. I can walk but suddenly lose muscle strength alot out of nowhere (especially if my vitals drop)
Doctors used to accuse me of inducing my symptoms through anxiety by constantly checking my finger monitor or blood pressure cuff. I don't even have to do those things anymore to know when I'm fluctuating in heart rate or blood pressure because I can feel my pulse and can feel the raises and drops in blood pressure, but I still get told I do, by people who don't even live with me.
Muscle twitches are still random and daily.
Doctors tell me to exercise to get strength and muscle back when in reality I was walking and moving around until I couldn't anymore because my strength and balance kept getting worse. I walked every night since I worked from home before this to try to avoid all of this.
I don't know what's going on in my body, I just want answers and to be able to walk, drive, and work again after over 3 years of having to be held by the hand for everything. I miss my independence, I miss my heart rate going down when I'm at rest, and up when I exert myself, not the reverse, and physical activity or exercise causing muscle growth instead of seemingly accelerating the muscle thinning, like if they no longer regenerate properly or absorb protein properly.
I'm tired of the fluctuations of blood test, telemetry, and circulatory tests causing doctors to ignore my results if they aren't consistent even if they're bad in the moment.
And my goodness I'm tired more than anything of family members and some doctors (not all mind you, I've met many professionals that aren't afraid to admit when they don't have an answer instead of the making up anxiety one) pushing the psych treatment anxiety/conversion route when I've taken every drug they've tried on me with no improvement in my symptoms and treated like everything from my fluctuating vitals to my lack of muscle strength, control, and equilibrium as just me lacking proper "emotional coping mechanisms" when I've taken psych meds they wanted me to take for years and even saw a counselor for awhile (it was required for my long term disability with private company for two years. Government disability and private company disability don't pay out anything if you don't take treatment, even if it's not needed.).
I'm currently trying to get in contact with a GI to be tested for issues with digestion or absorbing protein or other nutrients due to the lack of muscle growth even with attempted exercise at my age, and to find out why in the world foods like Pizza seem to make me worse (my first tachy episode, the calm before the storm if you will, was 135bpm after eating a pizza from little caesars, which I had done many times before, but for some reason shot up my vitals. That heart rate persisted the whole night even while I slept and I woke up sweating) I only had a colonoscopy and endoscopy in the past with a GI to check for possible internal stomach damage or cancer because of intense pain I had at the time that was never solved, but never did any testing for possible issues digesting and absorbing certain proteins or nutrients. Only thing for sure I know is taking antibiotics gives me sludgy poop like melted chocolate and made me feel sick, and stopping the antibiotics and eating yogurt made it better.
Any suggestions or help would be appreciated, all have left to go on concerning the muscle issues and equilibrium issues now is possible malabsorption issues since I don't have muscle wasting in my ck levels but definitely have had long term consistent muscle and balance loss, and possible intermittent intense vasoconstriction that can be short term or last (as of right now) over a week and could be affecting different areas of my brain.
As for autoimmune, I gave up on that route. Rheumatologist told me while my ANA is positive without having a narrower range of symptoms we would just have to keep conducting different labs for different autoimmune diseases until they find what it is (ANA tells you that you have autoimmune cells present, but not what condition they are for. Many autoimmune tests are very specific. Only comparison i have is my little brother who had a positive ana as well but only testing positive for Sjogrens. I was negative for that too)
And as for the vascular route with what my CTA results showed in Cleveland clinic, that hasn't helped because we have to "catch" the blood vessels and arteries in my head when they are like that, but it was only caught once, and common practice down here in South Florida is if the CT shows it but a later MRI on a different day does it, any further research on to the issue stops. The faintness, pulsing, and balance getting worse with neck or spinal bending/twisting is constant, but the pulsing does lessen if my vitals go up higher (such as getting up to walk a bit) and because of this it's at its worse when I'm trying to sleep or when I first wake up due to a natural drop in vitals when at rest.
As for anything else, I've had constant dripping from my nose down to my throat and out of my nostrils for almost a year now (when the equilibrium issues started getting worse), as well as chronic mucus and very minor throat infections, don't know why though.
Inflammation labs are normal, sed rate normal. I have yellow mucus alot but blood test almost never show a raise WBC indicative of infection. My poop has been constantly green and smaller for years since my symptoms started but where healthy, big and brown before that.
Lipomas started forming all over my body when my symptoms first started but I was told they're not an issue since they're benign, but man do they hurt when they press against a rib.
At the very least, I'm able to talk with my wife and enjoy movies and meals together again and can lessen the symptoms of i stay sitting or laying down so as to not stress anyone out.
I have more walking strength after the tachy stopped being constant but the balance issues and throbbing pulsing issues i have in the areas that showed the narrowing in my arteries in Cleveland only got worse, especially when bend. So I tend to hold my wife when I walk to maintain balance and be held if I suddenly fall or lose my physical sense of where I am (lack of equilibrium spikes, usually induced by a sudden neck bend)
Thank you so much for any doctor or person that has read this far and I hope you have a good day even just for taking the time to read this, let alone leave any response of possible doctors I can see.
submitted by ivan3295 to AskDocs [link] [comments]
2025.01.24 05:51 MasterpieceSouth880 Too tempting to resist, aren’t I?
 | submitted by MasterpieceSouth880 to CutiesAsian [link] [comments] |
2025.01.24 05:51 teenx83369 new album comes out and all of sudden we got expert critiques for pitchfork
 | idc what yall say i loved this album and i hope for him to play all songs @ tour submitted by teenx83369 to osamason [link] [comments] |
2025.01.24 05:51 Shadows236 Last chapter?
Is the area 11 the last chapter so far? How can I keep leveling the devotion, doing hard mode?
submitted by Shadows236 to HorizonWalker [link] [comments]
2025.01.24 05:51 Organic_Impress_7562 Dead mouse smell
There was a dead mouse buried at the bottom of my laundry basket and I can’t get the stink out of the clothes. I’ve washed several times with 5 litres of vinegar in each load, and again with lots of oxiclean. But our building machines do not have a soaking option and I think the water is set at lukewarm even on a “hot” wash.
Is there something else that I should try?
(There is a liquid product called Odoban which I’ve never used but thinking of buying.)
submitted by Organic_Impress_7562 to laundry [link] [comments]
2025.01.24 05:51 Britt_Dan_Barr So Sweet (OC)
submitted by Britt_Dan_Barr to zootopia [link] [comments]
2025.01.24 05:51 Friendly_Estate1629 HWY 85 Banner People
Every day on 85 I would see Anti-Vaxxers and Anti-Israel banners at the exact same spot (right by Good Sam). Election is over and they've suddenly vanished. I've always wondered who these people are and more importantly - who was paying them. Is this a case of foreign meddling with our elections or just run of the mill whack jobs who packed it up after November?
submitted by Friendly_Estate1629 to bayarea [link] [comments]
2025.01.24 05:51 Careless_Plantain111 So um first post but WHAT happends if JUDGMENT DAY was on your bday what would you do or be like!
と@○~○@と ( idk what to say here lmao)
submitted by Careless_Plantain111 to jesuschristouija [link] [comments]
2025.01.24 05:51 Low-Hand-6977 Mon Mon ( DoeGang ( K Town ) 🔱 ) Family Waits Outside Hospital. He Was Shot In Back During a Fight / Attempted Robbery , Ultimately He Was Pronounced Dead.
 | submitted by Low-Hand-6977 to Chiraqology [link] [comments] |
2025.01.24 05:51 Known_Masterpiece_23 dlsu fw ??
 | am i the only one who doesnt find this stuff funny or what submitted by Known_Masterpiece_23 to dlsu [link] [comments] |
2025.01.24 05:51 Audis-n-shit Sales tax on cars
[AZ] I have read a few articles saying how 100% disabled vets don’t have to pay license tax or registration fees when buying a vehicle (on one car) but I’ve also saw that it’s only if you use VA financial funding (I didn’t even know the VA can find you money for a vehicle loan) so I’m not sure which is correct. My question is, if I go buy a car from a dealer with a pre approval from navy federal, does that mean I can tell them to wave the sales tax (license tax) and registration fees? When I asked the dealer about the registration being waved he said “we have to add it on and then you go to the DMV and they’ll reimburse you to my knowledge” but I just found out about the sales tax (license tax) so I didn’t ask about that yet
submitted by Audis-n-shit to VeteransBenefits [link] [comments]
2025.01.24 05:51 desrochy Different Oil Thermostat?!
 | Help, I wanted to get the Mossleman Thermostat but my E92 N54 oil thermostat looks completely different than everyone’s. submitted by desrochy to BmwTech [link] [comments] |
2025.01.24 05:51 MysteriousAdvantage3 Live rn
if anyone enjoys binding of isaac come join me im live rn playing some isaac rebirth https://linktw.in/FjFEWY
submitted by MysteriousAdvantage3 to SmallYoutubers [link] [comments]
2025.01.24 05:51 StrawberryAutomatic4 Took this from home depot, don’t know what it is but now it’s my pimp cane
submitted by StrawberryAutomatic4 to HomeDepot [link] [comments]
2025.01.24 05:51 bot_neen Tele Zócalo Nocturno / 23 De Enero De 2025
 | submitted by bot_neen to Mexico_Videos [link] [comments] |
2025.01.24 05:51 goober0322 Autograph Identification
 | Hello! Can anyone help me identify the player’s autograph on the puck on the right? A friend came across it along with Hank’s on the left so I’m guessing they were signed around the same time. submitted by goober0322 to rangers [link] [comments] |
2025.01.24 05:51 galaxysbestpilot Kidney stone or infection??
I’m just gonna copy paste what I asked the other medical subreddits
A few months ago I had a uti that I didn’t treat because I didn’t have insurance. I thought if i drank enough water i could pee it out and avoid medical costs. Because of this, the symptoms started getting worse. I started getting debilitating back pain and sharp pains in my side, as well as blood in my urine. Eventually my friend who had a kidney infection in the past told me that my symptoms are a lot like what she had. So I finally decided to get “medical help” (buying a bunch of antibiotics off goodrx) and it eventually went away after going through 5 different antibiotics and a trip to urgent care. I learned a lesson in never treating utis lightly. Thankfully I have insurance now. Recently I felt another uti coming on after taking too long to pee after sex. I immediately ordered antibiotics and started taking them to prevent what I went through before. But it hasn’t seemed to help. I’ve been having debilitating back pain and sharp pain in my sides again. I also have blood in my urine and I’ve been getting increasingly nauseous. But I went to the emergency room yesterday and they found literally nothing. They did a CT scan, an ultrasound, blood work, and a urine culture. They said all of my organs look healthy and nothing was wrong. They did say they saw some inflammation in a part connected to my kidneys I think? I wish I could remember exactly what part it was that they said but I was too focused on the pain and the confusion from them not finding anything to really listen. They said that inflammation was not a cause for concern and sent me home with two prescriptions for pain. As soon as I got home I tried to go to sleep and I couldn’t move from how much my back hurt. I eventually fell asleep hoping that it would get better when I woke up. But when I woke up this morning I was still in a lot of pain. I took the pain killers and they didn’t do anything but turn it into a slightly duller ache. The intensity comes and goes in waves and nothing triggers it to be better or worse. I’m still nauseous and haven’t eaten a lot lately. There’s more blood in my urine. I don’t want to go back to the ER because they didn’t find anything the first time so I doubt they’d find anything the second time. My instincts say it’s still a kidney infection but that obviously can’t be it if they found nothing in my blood, urine, or scans and ultrasound.
Someone commented on another subreddit that it sounds exactly like a kidney stone. But wouldn’t they have seen that in the scans? I’m so confused. The back pain is not as horrible currently but that’s because I’ve been popping tylenol like tic tacs. The blood in my urine has increased since I first posted this to the other subreddits. I’m really hoping that the commenter was right and it’s just a stone and not an infection
submitted by galaxysbestpilot to KidneyStones [link] [comments]
2025.01.24 05:51 QiZhenyu I would really appreciate if you use this Tangerine Orange Key: 74900719S1
Hi there, I would really appreciate if you use this Tangerine Orange Key:
74900719S1
Get a CAD 50 bonus with this code. Thank you in advance, happy banking!
submitted by QiZhenyu to OrangeKeys [link] [comments]
2025.01.24 05:51 rubix_god95 Selling 1 ticket for 26th Jan. J block at MRP - 7.2k
submitted by rubix_god95 to Coldplaytickets [link] [comments]
2025.01.24 05:51 ThinMintButterfly823 All-Star Starter Votes: Mobley 4th in Player and Media Votes (only player outside 3 starters to receive media votes) 6th in Fan Vote
 | Mobley received 74 votes from his peers placing behind the starters, 28 more than the next player (Banchero). Banchero had more than double in fan votes so came up 4th in the weighted final tally. Mobley finished 5th in the final weighted score. Obviously votes don’t count toward reserve spots, but it seems realistic to say that Mobley is a shoe in this year. Jarrett was 8th in player votes, 9th in fan voting. (Tied in 5th with media voting at zero votes as no one outside the 3 starters and Mobley received media votes). He finished 8th in the final weighted score. submitted by ThinMintButterfly823 to clevelandcavs [link] [comments] |
2025.01.24 05:51 According-Major-5426 Need help to bounce back
Hi all I am male(26) had a relationship at work for about a year, was very serious and wanted to marry her But financially she is from well off family hence I asked that I would need time to settle myself, she agreed too. But for last few months she started saying her parents started seeing potential groom for her (indian arrange marriage scene) I asked her if she willing to pushback this pressure she initially seemed to do so but suddenly started behaving weird saying she could not withstand their pressure and doesn't see future with me. On the 31st we officially brokeup
Now thing is that i have to see her in office daily and no matter how much I try, I still cannot moveon completely as whenever I see her or hear her, my hearts skips a beat. I thought let some days go I would be normal but I still feel strong for her. I don't even like any other girl even if I try. Lately I found out that she talks with some guy on phone via a collegue wo now my heart sinked a bit
What to do here?
I m going to gym and trying to switch but in current economy it is taking time
submitted by According-Major-5426 to BreakUps [link] [comments]
2025.01.24 05:51 ArzelockPizzaMaster 3 years of active achievement hunting
 | submitted by ArzelockPizzaMaster to xboxachievements [link] [comments] |