Medical Advice Thread - Does this look infected?

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The imaging you've had done rules out most things, but one that likely wouldn't have been picked up by any of those tests is adrenal insufficiency. Your symptoms are a good fit. Tremors, Heat Intolerance, Rapid Heartbeat (usually secondary to compensation for sudden low blood pressure), Fatigue, Depression, etc... Do you ever experience abdominal pain (not from a known cause), unusual nausea, poor concentration (not related to lack of sleep or other known cause)? These can be additional signs of adrenal insufficiency. If it's mild it could slip under the radar, appearing as a constellation of seemingly unrelated symptoms. It would most likely be worth mentioning to your doctor.

I assume they have checked your thyroid levels? Many of your symptoms can overlap with hypothyroidism, but overall adrenal insufficiency is a much better fit. There is a well known phenomenon in medicine where if one has an autoimmune disease, it is that much easier to develop another autoimmune condition. If is not uncommon for people with autoimmunity to have 2 or 3 distinct autoimmune conditions. Since you have psoriasis autoimmunity against the adrenal gland or thyroid are a much higher probability than they would be for the average person. Also, the autoimmune tests they have done are rather limited. RF & ANA would only be useful for a few specific conditions. A broader autoantibody panel may be more useful.
I'll ask her about it. I've had my thyroid tested a bunch of times and it's normal. Yes I do experience those things. Isn't adrenal insufficiency a crunchy diagnosis or do you mean the real one? I know it's both a real diagnosis and a one crunchies use to explain anything, along with "leaky gut" and "chronic lyme". How do they test for adrenal insufficiency? That's a good suggestion, there seems to be so many types of autoantobodies. I didn't know they could do whole panels on them.
If it's actually in your ass, a colonoscopic extraction is probably the best bet. If you're talking about eating a burger, and the size of your ass got bigger, then just less calories and exercise. However, depending on the size of the ass, one may not want to do anything. What many women consider a problem regarding the magnitude of one's ass, many men would consider beneficial. Food for though (not for the ass).
@Burgers in the ass Finally we have the knowledge to save you!
 
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I'll ask her about it. I've had my thyroid tested a bunch of times and it's normal. Yes I do experience those things. Isn't adrenal insufficiency a crunchy diagnosis or do you mean the real one? I know it's both a real diagnosis and a one crunchies use to explain anything, along with "leaky gut" and "chronic lyme". How do they test for adrenal insufficiency? That's a good suggestion, there seems to be so many types of autoantobodies. I didn't know they could do whole panels on them.

@Burgers in the ass Finally we have the knowledge to save you!

The real one, known as Addison's Disease, although Addison's Disease is technically only primary adrenal insufficiency. There are secondary and tertiary adrenal insufficiency as well. Where in the HPA axis (Hypothalamus, Pituitary, Adrenal gland) the insufficiency is coming from, and each type is caused by different things. They can be distinguished by lab work that check CRH, ACTH, DHEA, DHEA-S, Cortisol, Aldosterone, Renin, Sodium, & Potassium. Which ones are high and low indicate which type of adrenal insufficiency it is, if it is present.

The crunchy one is known as "Adrenal Fatigue" and, as you know, complete nonsense.
 
Actually I thought about it harder, I don't get much nausea and stomach pains. I feel like I would see this darkening of gums and stuff from Addison's disease.
 
Actually I thought about it harder, I don't get much nausea and stomach pains. I feel like I would see this darkening of gums and stuff from Addison's disease.

That's why I mentioned Addison's disease as the archetype of the disorder, and is representative of only primary adrenal insufficiency. Hyperpigmentation is not seen in secondary nor tertiary adrenal insufficiency.
 
@lurk_moar I'm relieved that you think it's nothing to worry about!:heart-full: I think I'll end up having to pay for the antibody test privately, but glad to hear that you think the lympho and basophil counts are relatively alright.

@Manul Otocolobus It wasn't a silent UTI, I am just so used to being unwell/untreated/in pain that I didn't register it as abnormal (:_( I was given a 3 day course of nitrofurantoin (via the phone, empirically) to treat uncomplicated symptoms in February 5, and the doctors at ED presumed that it hadn't been completely cleared and was currently ascending to kidney, causing the tachycardia. In over almost 14 years of chronic uro shit happening (and now 3 kidney infections, one of which ended me in the ED), my GP has never seen fit to refer me to a urologist. They usually treat all LUTS the same, take the antibiotics and gtfo (no cultures because fuck patients, thats why). You're kinda left on your own, stuck in an eternal cycle of getting infection, going to gp, getting it treated (and hope it works), recover (or not, screw you there's no follow up because they don't take cultures unless you are septic in ED), or wait 2 weeks to see a doctor again.

I ended up in the ED again on the night of thursday to friday, with the same presentation as on Sunday (I got told on Sunday to ring again if I was still having issues after 5 days of antibiotics, so I did). Paramedics came in, tachy all over the place, abnormal ECG. At the hospital, one abnormal ECG, one "normal" ECG, and blood tests all clear for heart damage, infection seems to have cleared as well. But I still feel faint, get palps, get dizzy on standing up, etc, etc. All of this shit was triggered by sitting in the bath, for god's sake. This time the attending doctor suggested I had anxiety, and should head back to my shrink to sort out either the ADHD medication dose, or get some more therapy.

At this rate I have 3 different ECGs taken by paramedics indicating stuff that should be investigated properly, but again, because of cost cutting there's no way in hell I'd ever be referred for a stress test or an ultrasound or anything. One of the paramedics told me that in order for the NHS to consider referring someone to a cardiologist, someone must have ended up in the ED two times or more with signs of ECG trouble AND bad blood results AND chest x ray etc. So I guess I'll have to crawl back to my GP, hope they can help (or my poor psych doses me up enough to tolerate ambulance-worthy symptoms), and eventually scrounge up the money to see a cardiologist out of pocket.

So by now you must have a pretty clear idea of how it works here: cost cutting potentially putting patients at risk, and in my personal case, their negligence has left with a bladder so trabeculated by chronic infections that I already have to get up to piss during the night hah! (I only discovered this after paying out of pocket to see a private urologist who actually did a cysto and flow test, establishing that I had neuropathy there, leaving me more vulnerable than average).

Naturally, after this I'm reticent about any NHS doctor's opinion on my health. It sucks to feel like you can't trust your docs at all, but where I live you have to lie, beg, cheat and steal for a chance to get proper healthcare (without going private). It's exhausting to have to constantly check shit for yourself (and horrible for anxiety too!), but I'm not fucking around with cardio issues especially when I'm on stimulants and all that.

No urology follow up. No thyroid antibody testing. No cardio investigations, let alone giving any advice whatsoever on how to cope with a bout of palpitations at home.

Gonna have to get in on that meditation and yoga! I will try to stick to everything else that you have recommended. Would I be okay to use a cold pack to try and bring down the bpm? Normally I feel the palps thudding in my neck and ear, but anything higher than 115 seems to give me chest pain.
 
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I'm really quite surprised they went with nitrofurantoin. The incredible increase in resistance that has been seen around here has removed it as a first-line treatment. Typical first line treatment now is TMP-SMX (trimethoprim/sulfamethoxazole) or a cephalosporin like ceftriaxone (I probably wouldn't pick a 1st gen like cefalexin since it is known for having incomplete activity against some e. coli). The fact that the nitro caused incomplete resolution would be seen commonly now. The lack of culture is just wrong and scary. There are quite a few reasons (in addition to the one I mentioned above) why Keflex could fail, especially after an initial failure with abx therapy. I would also disagree with them classifying it as "uncomplicated". With your history of LUTS and pyelonephritis, thinking it is an "uncomplicated" case without any proof is negligent. Your history alone should have excluded nitrofurantoin as a first choice.

I just don't see the methylphenidate being the source of this. You've been taking it for some time, correct? No recent dosage changes? If so, sudden onset tachycardia to a medication you've been on and had no trouble with just doesn't happen with no change. The duration also doesn't make sense. If it was triggered by the methylphenidate, then the onset and duration of the tachycardia should match what's known as the pharmakokinetics of the medication. Pharmacokinetics is how a medication is usually metabolized, so when and how long it works for is well known as it typically doesn't vary (too) much between people.

If you do indeed have subacute lymphocytic thyroiditis, it is possible you've "flipped phases", which is known to happen. When this occurs you can actually switch from hypothyroidism to hyperthyroidism, with one of the main symptoms being palpitations and abnormal cardiac rhythms (arrhythmia). Unfortunately a bath can trigger exactly what you experienced because it also causes moist heat intolerance.

The reason you feel dizzy or faint is that when one crosses the tachycardia threshold that is the point where the heart starts to lose efficiency, and as the rate goes up, efficiency drops respectively. The reason for the efficiency drop is that the heart is beating so fast that it isn't filling up to full capacity before it tries to push the blood out, so not enough oxygenated blood is being circulated. With an insufficient amount of blood circulating suddenly your body is no longer getting the proper amount of oxygen, which starts to cause all sorts of impacts on the various organs and systems. Since the brain is our most energy intensive organ, and it requires a constant, uninterrupted supply of oxygen to work correctly, it is most impacted by a sudden lack of available oxygen to meet demand.

You'll definitely want to avoid hot baths, and showers that are hot as well. Tachycardia, due to lack of cardiac efficiency, will make one feel dizzy or faint, exposure to hot water just makes it that much worse or can possibly trigger it. When one is exposed to that kind of heat, it causes a "steal" effect where the peripheral vessels expand to try and deal with the heat, which shunts the blood into the peripheral circulation. So, the blood is shunted into the peripheral circulation, and tachycardia is causing a loss of cardiac efficiency. If they are put together, one has a situation where there is not nearly enough blood flow in central circulation. Sitting of lying down, one is generally ok, but as soon as they stand up, they will get very dizzy or faint, because the lack of proper central circulation will cause the phenomenon known as orthostatic hypotension to kick in. Normally when one stands up, the heart rate elevates slightly to compensate for the fact that the blood pressure in the central circulation is suddenly trying to drop. If one isn't experiencing tachycardia at the time, this sudden attempt to raise the BP while the blood is in the peripheral circulation can actually trigger it. However, if one is already experiencing tachycardia, any attempt to further increase the heart rate just exacerbates the problem by making the heart even more inefficient, which actually causes blood pressure to fall further. If BP drops below a given threshold, one will experience syncope, which is where the brain isn't getting enough oxygen to maintain consciousness, causing the person to black out and hit the floor. Blacking out is a bad thing, but it is the body trying to correct the sudden problem it is experiencing the only way it can. By causing the person to suddenly hit the floor the problem of low BP is corrected because the person is no longer standing, which was causing the low BP condition. The heart can stop trying to accelerate further, and as soon as the oxygen debt caused by the hypoxia in the brain is resolved, the brain brings the consciousness back online and the person wakes up, suddenly wondering why they are lying on the floor when the last thing they remember is standing up. Of course, taking a fall from blacking out is dangerous, but it's a better alternative than what would happen if the oxygen debt in the brain wasn't rapidly corrected. That's why it's just better to prevent the entire situation by avoiding hot water altogether.

If you find just standing up from lying down is enough to trigger a tachy episode due to HR acceleration to stabilize BP, the best way to avoid that is to go from lying down to sitting, wait a handful of seconds, then stand up slowly. It allows your body to adjust BP in stages instead of all at once and should hopefully prevent a tachy episode. Did they happen to tell you what was abnormal about the ECG? What it actually said or indicated is key. There are many forms of tachycardia, but an ECG capture would go a long way to determining what is going on.

It's funny you mentioned an ice pack, because ice (or ice water) can be involved in one specific way to break tachycardia. Why they haven't told you these things is beyond me, it is bog standard for them to tell anyone how to do these things that has experienced a series of tachycardic episodes. One way to break tachycardia is to put ice packs or a plastic bag of ice on your face for about 15 seconds. If that doesn't work you can immerse your face in ice cold water for several seconds. If that fails a cold bath or a cold shower might work. However, you can't spend much time in a shower or bath of cold water because your body temp will start to lower and that can trigger a reflex tachycardia as a way to try and warm you up. A different way to trigger your heart rate to drop is to activate your gag reflex. I generally recommend using a tongue depressor to do it (or a popsicle stick) . You can use your finger, just make sure to wash your hands first. The gag reflex works because it increases the tone of your vagus nerve, which will drop your heart rate. Yet another different way is to cough really hard, and keep doing it until your heart rate comes down (or it seems unreasonable to do so any longer/you get no response from it). This also increases the tone of the vagus nerve. Another thing to try is to hold your nose, close your mouth, and try to force the air out (it's the trick ENT's teach people to clear their eustachian tubes when they are clogged). It also will increase your vagus nerve tone. The very last thing to try, because it is the most difficult, is carotid massage. Make sure you are lying down for this one since it can cause your BP to suddenly drop. You need to find your carotid pulse (the pulse in your neck), once you can do that, trace it in essentially a straight line to your jaw, then go back down that line about an inch. You should still be able to feel your pulse strongly at that spot. This is where your carotid sinus most likely is. You want to firmly massage that area, only on one side. If you're in the right spot, it should strongly influence your vagus nerve and cause your HR to drop.

Despite being an American, without PLing, I am fairly familiar with the NHS system, but it was a few years ago. Though, I still have a number of colleagues/friends who are part of the Bri*ish medical community. I knew there were cutbacks, but I had no idea it was this bad. I mean, the NHS wasn't great back then, but it sounds downright criminal now, in an almost literal sense. I don't know how they can get away with treating patients like this. Have the cutbacks gotten precipitously worse due to COVID? Unfortunately I haven't been able to keep up nearly as as well as I would have liked the last few years.
 
I'm so sorry I keep shitting up the thread, maybe we should find a better way to do this :(

@Manul Otocolobus you're out here doing the Lord's work, God bless!

Yep, I've been on the methylphenidate since about October 2021. No previous history of high blood pressure, or any other heart disease. I've fainted three times in my life (before this medication). Once from hypovolemia during a blood draw, and twice after standing up too fast after a waterpipe session, both times. I got up, feeling okay (not drunk, just smoking), walked unsteadily for 3 mins, keeled over. Ended up getting checked out by paramedics both times, who said I had low blood pressure - now it kinda makes sense why :(

I think the anxiety is bullshit too, because whenever I have had actual chest pain or palps, I measure the BP and BPM every 30-40 mins all the while making conscious attempts to distract myself (like watching TV), I make a point of waiting for 1 to 2 hrs just to make it isn't a panic attack, but apparently presenting with 138 bpm on a taken ECG after 2mg diazepam (and by then the paramedics had given me codeine too, so I was chilled the fuck out) is still anxiety?

I have had anxiety attacks in the past, I know what those feel like. This isn't that. And I'm certainly not so stressed that I can maintain tachy for over 6 hours for god's sake.

I have no idea about the thyroid anymore. Nobody seemed to give a shit about a history of thyroid fuckery in the family, or the blood results I shared here, or anything at all really. All they cared was that they could "safely" discharge me according to guidelines (troponin okay, latest ECG "normal" or signed off by a doctor). If anything, the doctor that saw me seemed annoyed that I could provide him with actual snapshots of my heartrate and BP over this week. I'm sure they thought I'm just a neurotic woman with health anxiety lmao. As usual, no paperwork to hold on to, no paper trail, no real names, no accountability. The doctor that saw me this last time didn't even seem to be aware that I had been there earlier this week and he could access that medical history if he needed to.

Funny story: I actually asked that doctor straight up "okay, so its anxiety, what can I do to bring down my heart rate during a "panic attack"?" and he said "hmm its difficult, have you tried meditation?"
I suspected that he wouldn't bother to give me vagal maneuvres without prompting, but this just made me feel even more dubious about the whole thing. Thank you for confirming that these are something I should be able to do safely. I actually used the cold pack on my face this last time (it helped somewhat but didn't solve it).

The only thing regarding these AE stays is the paperwork that the paramedics gave me from when they took both initial ECGs. I have no idea how to read these, so I will type up what the printout says:

27 Feb
130 bpm
Sinus tach
left atrial abnormality
rightward electrical axis
ST-T abnormality, consider inferolateral ischemia or left ventricular strain
abnormal ecg

4th March:
138 bpm
Sinus tach
T wave abnormality, possible inferior ischemia
abnormal finding for 18-39 female

Should I go to a private PCP and show them these ECGs and push for a cardiologist referral?

Yeah, the NHS situation as a whole is nothing short of atrocious. There's a bunch of social factors at play in the UK that keep the NHS from being heavily reformed, and it has become a government budget blackhole. Every year it gets worse and worse, and the only solution anyone can think of is to just throw (still not enough) money at it.

You already know a little about the healthcare failures, pretty much. The reason nitrofurantoin and cefalexin are prescribed empyrically (and seemingly without much thought) is because NHS doctor's here are generally required to provide treatment according to NICE guidelines. Here are the guidelines for UTIs and Pyelo specifically (under recommendations tab). I am "lucky" in that I tend to get nitro these days without just having to explicitly turn down treatment with TMP (just TMP) first (which is a complete waste of time, as far as I'm concerned, it only worked for my first UTI ever).

The NICE guidelines are meant to be effectiveness-tested, and help keep costs down but usually what happens is that anyone who needs a thorough workup gets left to either deteriorate enough to actually get NHS treatment, or pays out of pocket to get relief.

In addition to that, I had to wait 6 hours in the ambulance with the paramedics (with chest pains) before they could even take me inside for the first ECG at the hospital. ED block was full, ambulance beds full, even resus was full. They had people on drips in the waiting area because there were no beds, or even chairs for us. Even the nurses who looked after us admitted that they should be doing ECGs on stretchers instead of chairs. They wanted to do a repeat ECG right after my first one at the hospital, but the machine was nicked while the nurse was gone (she was looking after 5 people for the 30 mins I was actually in resus before they send me back out to the WR). It was atrocious and I was glad I wasn't actually dying, holy shit!
 
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Ok, this problem has been stumping me.

I got my A1C checked at work, and it was 4.3 which is an average blood glucose of 77 mg/dl. It has never been this low before. My A1C values range from 4.6 to 4.9. I do calorie restriction, high protein, low carb diet, and lift weights. Could my weight lifting cause my hypoglycemia? I basically eat no carbs. I have PCOS with frequent hypoglycemia. My random glucose levels used to be in the 80's. The highest my random glucose has ever been was 110 mg/dl. Are my insulin levels way too high? I seem to suffer from hypoglycemic symptoms after lifting weights.
 
Ok, this problem has been stumping me.

I got my A1C checked at work, and it was 4.3 which is an average blood glucose of 77 mg/dl. It has never been this low before. My A1C values range from 4.6 to 4.9. I do calorie restriction, high protein, low carb diet, and lift weights. Could my weight lifting cause my hypoglycemia? I basically eat no carbs. I have PCOS with frequent hypoglycemia. My random glucose levels used to be in the 80's. The highest my random glucose has ever been was 110 mg/dl. Are my insulin levels way too high? I seem to suffer from hypoglycemic symptoms after lifting weights.
try eating a balanced diet instead of completely cutting out certain foods.
 
Ok, this problem has been stumping me.

I got my A1C checked at work, and it was 4.3 which is an average blood glucose of 77 mg/dl. It has never been this low before. My A1C values range from 4.6 to 4.9. I do calorie restriction, high protein, low carb diet, and lift weights. Could my weight lifting cause my hypoglycemia? I basically eat no carbs. I have PCOS with frequent hypoglycemia. My random glucose levels used to be in the 80's. The highest my random glucose has ever been was 110 mg/dl. Are my insulin levels way too high? I seem to suffer from hypoglycemic symptoms after lifting weights.

Why calorie restrict? When you say "at work" do you mean they did your A1C with one of those portable gizmo's or an actual medical laboratory? If it was with the portable ones, they are well known for having a large confidence interval, which makes them fairly unreliable when it comes to the finer degrees of measurements. If you mean medical laboratory, then there is a good chance it is accurate. As a general rule people dealing with hypoglycemic episodes should never calorie restrict as it can just exacerbate the risk of hypoglycemic swings. Why do you avoid carbs? Do they tend to trigger hypoglycemic swings? Your instantaneous/random glucose is with no eating 12 hours before? If not, how long after eating? Postprandial glucose can be useful, but not quite as useful as fasting blood glucose. Hypoglycemia post anaerobic exercise is not surprising. If your blood glucose was borderline before the exercise, the exercise itself will likely trigger a hypoglycemic episode. If you are building muscle, that is likely what is causing your A1C to drop. Muscle increases basal metabolism, which will create a continuous demand on blood glucose. To try and stem the hypoglycemia it would probably benefit you to consider a eucaloric diet in consultant with your primary care physician. Even if your BMI is above 25 (the most common reason for caloric restriction), until you can get the hypoglycemia well defined or under control a eucaloric diet would likely be beneficial.
 
try eating a balanced diet instead of completely cutting out certain foods.
Agree with snail. Try to incorporate healthy complex carbs but don't cut out full food groups. Keep cutting out the refined carbs like you're already doing cus no one really needs those. Complex carbs are really healthy and keep your blood sugar stable for a long time. Roast veggies, whole grain bread etc.
 
Pls ignore facedox and tell me how bad my allergic reaction is:

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If the tongue is protruding from swelling, imminently life threatening. I probably wouldn't even attempt a fibre scope, I'd probably go right to a crash trach to ensure we had an airway.
Don't worry, this was just a joke. This is a munchie girl from the Munchausen's by Internet thread who fakes MCAS and anaphylaxis very poorly. Credit to @Kate Farms Shill for making me laugh with that pic.
 
2021 and still no cure for autism, we are fucked :(
OK in seriousness, does anyone have thoughts on autism treatments? I have multiple people in my life who are on the spectrum (maybe we all are). I imagine a lot of the ideas I see online don't really work, like special diets or supplements...but maybe one of them does? The more "science-y" resources all say none of that stuff works but here try an SSRI or ADHD drugs which doesn't sound great either.

A lot of the behavioral stuff for adults I have found seems to be aimed at medium functioning folks. Any good resources for higher functioning people?
 
OK in seriousness, does anyone have thoughts on autism treatments? I have multiple people in my life who are on the spectrum (maybe we all are). I imagine a lot of the ideas I see online don't really work, like special diets or supplements...but maybe one of them does? The more "science-y" resources all say none of that stuff works but here try an SSRI or ADHD drugs which doesn't sound great either.

A lot of the behavioral stuff for adults I have found seems to be aimed at medium functioning folks. Any good resources for higher functioning people?
Reluctant to PL, but I was personally told that medications like Lithium Carbonate to treat depression and anxiety are also used for HFA.
 
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