Curious if anyone has health weirdness

LJSDesigns

Sweet Shoppe Designer
I went to the doctor today because I haven't been feeling well, and long story short, turns out I have a soft tissue infection again. This is my fourth one is the last few years and I have no idea how I get them, there is never a break in the skin like you would think with a regular infection, but I get them. This on is on the back of my leg just up from my knee which sucks because it hurts to touch, ie sit on, wear clothes, etc.

On top of that, apparently I have an ear infection as well, so I am double whammied. Weird thing is my neck hurts, but not my ears or throat which one would think would hurt with an ear infection, not the neck. I told the doctor my neck hurt, but my ears only itch a little. She says she is not surprised because I am atypical, ie. weird.

This weirdness is inherited from my father and starts with a low body temp and goes all the way to the point that things aren't always where they are supposed to be in my body. For instance, my thyroid was under my collar bone and my cervix used to be tilted sideways.

I also tend to have strange reactions to things as well, for instance, I don't dissolve dissolvable stitches. They will move through my body until they find a way to come up and out. I get a sore that starts to fester and then the stitch will pop out. It is disgusting to say the least.

So after my visit to the doctor and what she said about me being atypical, it got me to thinking, surely I can't be the only one who has stuff like this happen or has parts in the wrong place, right?

So if you are weird like me, I want to hear about it so I feel less like a freak of nature. LOL
 
I have lots of little things that need addressing, but nothing out of the box. I too have a low body temperature amongst a host of other things, but I think it all relates to my thyroid. Maybe consider checking your gut health. Probiotics etc could be helpful? I've never heard of anyone who can't dissolve stitches. :huh:
 
My mom always says she is a freak... lots of things that leave doctors saying, "I don't know..." My grandma's heart was backwards... and I take after her a lot in physical stuff... I often wonder if mine is too - but no doctor will check because I don't have heart issues.

My knee cap slides sideways... two of my wisdom teeth are missing (my mom didn't have wisdom teeth, but they found bone chips in different parts of her body that they are assuming was her wisdom teeth).
 
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The longer I am out in the world (aka, the older I get and the more people I interact with), the more I realize there is no "normal." There may be "typical," but that word just means "this has been recognized more often--or more voraciously--by others."

Having said that, I too have a low temp! So, according to this thread, 3 out of 4 of us have a low temp...which would make us the Typical Temps. Take that, Medical Establishment! lol
 
I have lots of little things that need addressing, but nothing out of the box. I too have a low body temperature amongst a host of other things, but I think it all relates to my thyroid. Maybe consider checking your gut health. Probiotics etc could be helpful? I've never heard of anyone who can't dissolve stitches. :huh:

Thyroid issues are the pits (thyroid cancer survivor) and I don't think people realize how much it impacts, so it is smart to get that stuff checked.

That is another one, I didn't mention. My thyroid did not uptake iodine like it was supposed to so the radiation I had went to my spine instead. Didn't see that one coming, but I had to go through a lot of physical therapy to stand and walk again and I lost over an inch in height because of it.

I do take stuff for my gut health because once I hit fifty things stopped working like they should.

As to the stitches, nope, can't dissolve them at all. Like I said, weird.
 
My mom always says she is a freak... lots of things that leave doctors saying, "I don't know..." My grandma's heart was backwards... and I take after her a lot in physical stuff... I often wonder if mine is too - but no doctor will check because I don't have heart issues.

My knee cap slides sideways... two of my wisdom teeth are missing (my mom didn't have wisdom teeth, but they found bone chips in different parts of her body that they are assuming was her wisdom teeth).

Wow, a backward heart has to be some serious stuff. I hope it did not impact her as much as I am thinking it would have.

Does it hurt when the kneecap slides? If they find bone chips in you, then we will know you took after your mom, halfway at least. LOL That is really interesting to know they were there, just not the way they were supposed to be there.
 
The longer I am out in the world (aka, the older I get and the more people I interact with), the more I realize there is no "normal." There may be "typical," but that word just means "this has been recognized more often--or more voraciously--by others."

Having said that, I too have a low temp! So, according to this thread, 3 out of 4 of us have a low temp...which would make us the Typical Temps. Take that, Medical Establishment! lol

Good point, Sara! LOL I think the low body temp is common which makes me think that the standard may be wrong. I mean, Pluto is not longer a planet, so anything is possible, right? LOL
 
I have a lot of "not normal" stuff, but thankfully like stated above, we are all unique and there is no "normal" especially since all of our bodies are vastly different. I'm just thankful our doctors are able to treat all of our differences without overlooking (for the most part) any symptoms/signs.

One thing that comes to mind is that I have an extra rib/bone that goes up and in to my clavicle, which makes it hard for doctors to check the glands around that area because there is a bone sticking out. Up until recently we thought it was just on one side of my body, but apparently last year they discovered I have the same thing on my other side, just not as pronounced as the other.

I do not have a lower body temperature, but I do have low blood pressure to the point that 120/60 feels like I am going to die. Normal for me is somewhere in the 90's....my eldest's is lower than mine, which is really scary combined with her other medical issues.
 
My hubby is "weird". He's got organs that aren't in the "proper" place and low body temp too.

I don't have anything that I can think of off hand right now
 
I have a weird one- Chronic Idiopathic Urticaria(CIU)/dermatographia- basically means I break out in hives for no reason. SUPER fun! It flares up every few years where it starts with my hands, feet & scalp getting itchy and then whatever is tight on my skin (bra, socks, waistbands, etc) will break out in hives. I'm then a human chalkboard- you can literally scratch on my arm a word & it'll hive up. It is possibly THE WORST form of torture- to be itchy, unable to scratch (they get MUCH worse when scratched) and very very little to do to help. I often wake up at night scratching or rubbing my hands together - so then they swell all up. It's tortuous. When it flares, it never fails to be while I'm on vacation, or a holiday weekend so I end up at an urgent care and usually on high dose of Prednisone (the worst drug ever!) I've done crazy amounts of allergy testing (I'm allergic to everything) and never have we been able to pinpoint an exact source/cause of the hives. My body is just weird is hyper-reacts to everything... :/

My current regimen of antihistamines is:
24hr Allegra, (2) in the am, (2) in the pm
Famotidine (2ndary antihistamine) (1) am, (1) pm
Singular/Montelukast (1)am
Nasacort (1) spray am, (1) spray pm

So far it's been a bit since my last flare up- but **knocking on wood** I feel like I'm on a pretty stable regimen considering my normal seasonal allergies have been okay during a crazy high pollen season.
 
Good point, Sara! LOL I think the low body temp is common which makes me think that the standard may be wrong. I mean, Pluto is not longer a planet, so anything is possible, right? LOL
And I now see the earth has a fifth ocean.
I don't register any blood pressure when I'm super sick. Like I'm dead! My mom was that way too.
 
I have a lot of "not normal" stuff, but thankfully like stated above, we are all unique and there is no "normal" especially since all of our bodies are vastly different. I'm just thankful our doctors are able to treat all of our differences without overlooking (for the most part) any symptoms/signs.

One thing that comes to mind is that I have an extra rib/bone that goes up and in to my clavicle, which makes it hard for doctors to check the glands around that area because there is a bone sticking out. Up until recently we thought it was just on one side of my body, but apparently last year they discovered I have the same thing on my other side, just not as pronounced as the other.

I do not have a lower body temperature, but I do have low blood pressure to the point that 120/60 feels like I am going to die. Normal for me is somewhere in the 90's....my eldest's is lower than mine, which is really scary combined with her other medical issues.

I think the not normal thing is why my doctor always says I'm atypical. LOL

I've heard of extra ribs before, but am trying to picture it sticking up into your clavical. What I picture hurts, but I am sure I am not seeing it for what it really is. It doesn't poke out at all, does it?

I am starting the think the lower body temp is pretty typical after all.
 
My hubby is "weird". He's got organs that aren't in the "proper" place and low body temp too.

I don't have anything that I can think of off hand right now

Ah, those wandering organs. They can be just about anywhere once they get loose. ;)
 
I have a weird one- Chronic Idiopathic Urticaria(CIU)/dermatographia- basically means I break out in hives for no reason. SUPER fun! It flares up every few years where it starts with my hands, feet & scalp getting itchy and then whatever is tight on my skin (bra, socks, waistbands, etc) will break out in hives. I'm then a human chalkboard- you can literally scratch on my arm a word & it'll hive up. It is possibly THE WORST form of torture- to be itchy, unable to scratch (they get MUCH worse when scratched) and very very little to do to help. I often wake up at night scratching or rubbing my hands together - so then they swell all up. It's tortuous. When it flares, it never fails to be while I'm on vacation, or a holiday weekend so I end up at an urgent care and usually on high dose of Prednisone (the worst drug ever!) I've done crazy amounts of allergy testing (I'm allergic to everything) and never have we been able to pinpoint an exact source/cause of the hives. My body is just weird is hyper-reacts to everything... :/

My current regimen of antihistamines is:
24hr Allegra, (2) in the am, (2) in the pm
Famotidine (2ndary antihistamine) (1) am, (1) pm
Singular/Montelukast (1)am
Nasacort (1) spray am, (1) spray pm

So far it's been a bit since my last flare up- but **knocking on wood** I feel like I'm on a pretty stable regimen considering my normal seasonal allergies have been okay during a crazy high pollen season.

Sounds like your hives are like my soft tissue infections as in there is no good reason for it to happen, it just does. I totally understand what you are saying about the hives though, because I get them too. Today, I was itching like crazy and ended up taking some benedryl to help. I am lucky cause that usually does it for me, so I am no where near what you are going through. You totally have my sympathy on that one.
 
And I now see the earth has a fifth ocean.
I don't register any blood pressure when I'm super sick. Like I'm dead! My mom was that way too.

I am not sure which statement is more surprising, a fifth ocean, which I have not heard about, or no blood pressure. That has to freak people out for sure. Do you have really thin arms? Maybe they just can't get the pressure they need in the cuff for the test? Just guessing here.
 
I'm curious what people are considering a low body temperature. I've read that body temperatures have been going down, in general. I'm consistently at 97.7F (36.5C) taken orally, which is pretty typical. The most accurate method is rectally, which I know isn't a common way to measure, lol. Everyone I know is always super low with temporal measurements.
 
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I'm curious what people are considering a low body temperature. I've read that body temperatures have been going down, in general. I'm consistently at 97.7F (36.5C) taken orally, which is pretty typical. The most accurate method is rectally, which I know isn't a common way to measure, lol. Everyone I know is always super low with temporal measurements.

I have to take mine every day at work before I start and it is usually 95.4 taken with the scan gun thingy, which I am sure is probably off a bit, but the highest it has even been when I feel fine is 96.8. It is interesting that the temps have been going down. Wonder what is causing that. My son told me the other day that the sperm count in men is also on a downward trend. I wonder how many other "body" things are changing too.
 
Here's the fifth ocean article:
https://www.nationalgeographic.com/...cean-now-can-you-name-all-five-southern-ocean


A paramedic told me once that he couldn't get a reading on me, so I assume it happens when I'm super sick because it happened to my mom when she got really ill.

Thanks for sharing the article; very interesting.

Genetics is so much fun, isn't it. I get all my weirdness from my Dad. He was atypical as well and had a very rare disease. Thankfully I did not get that from him. When I was doing genealogy, I traced his mother's and father's lines back and found that both descended from the same family; a brother and sister from the early 1600's. The line did not reconnect until my grandparents and I believe the recessive gene that the siblings carried and my grandparents carried was what caused my dad's illness. This has played out further for me because my uncle has the same illness, which is prevalent in males. Finally, my grandfather's niece married my grandmother's brother and they have children with the same rare, genetic disease. Because of this history, I have always been fascinated by genetics.
 
I think the not normal thing is why my doctor always says I'm atypical. LOL

I've heard of extra ribs before, but am trying to picture it sticking up into your clavical. What I picture hurts, but I am sure I am not seeing it for what it really is. It doesn't poke out at all, does it?

I am starting the think the lower body temp is pretty typical after all.
Sometimes it hurts and feels like bone on bone rubbing, especially if I move my arms around a lot or doing heavy lifting. The bones don't poke out, but if I were to lose an ideal amount of weight it would be noticeable to people that my neck/clavicle area doesn't look like other people
 
oh wow, yeah low temp here too. When I feel like I have a fever I am at 99 because I am usually at 96. LOL!!!
 
oh wow, yeah low temp here too. When I feel like I have a fever I am at 99 because I am usually at 96. LOL!!!

Totally! LOL My dad was deathly ill at 101. I don't think I am as low as he was though, but if I get over 100 I feel like I am burning up.

If this thread proves one thing, it's that the standard temp is not that standard. LOL
 
I went to the doctor today because I haven't been feeling well, and long story short, turns out I have a soft tissue infection again. This is my fourth one is the last few years and I have no idea how I get them, there is never a break in the skin like you would think with a regular infection, but I get them. This on is on the back of my leg just up from my knee which sucks because it hurts to touch, ie sit on, wear clothes, etc.

On top of that, apparently I have an ear infection as well, so I am double whammied. Weird thing is my neck hurts, but not my ears or throat which one would think would hurt with an ear infection, not the neck. I told the doctor my neck hurt, but my ears only itch a little. She says she is not surprised because I am atypical, ie. weird.

This weirdness is inherited from my father and starts with a low body temp and goes all the way to the point that things aren't always where they are supposed to be in my body. For instance, my thyroid was under my collar bone and my cervix used to be tilted sideways.

I also tend to have strange reactions to things as well, for instance, I don't dissolve dissolvable stitches. They will move through my body until they find a way to come up and out. I get a sore that starts to fester and then the stitch will pop out. It is disgusting to say the least.

So after my visit to the doctor and what she said about me being atypical, it got me to thinking, surely I can't be the only one who has stuff like this happen or has parts in the wrong place, right?

So if you are weird like me, I want to hear about it so I feel less like a freak of nature. LOL

There is no ugliness in you. It just has its own peculiarities, which, unfortunately, sometimes cause inconvenience. If you judge so, each of us has our own problems. I have now been diagnosed with autoimmune thyroiditis. So there was a reason for my increased fatigue, slow metabolism and excess weight. Now I have to undergo lifelong hormone therapy. But you can live with it.
 
This is so interesting to me. I'm missing a chromosone that makes me wake up from certain anestesia. We found this out when I took 45 minutes to wake up from getting my tonsils out when I was in college; they made me wear a med alert bracelet after that because it was so dangerous. Fortunately, I've never had any issues with it since, but the doctor said if I was exposed to that drug again, I might not wake up!
 
I have naturally low blood pressure. When I am at a healthier weight, it's low enough to make me get light-headed and dizzy often. There's also some extra bone on the inside bottom of my mouth. It makes dental work more difficult but doesn't affect me normally. The dentist mentioned to me recently that if I have to get dentures, they would have to cut that bone out! I will never get dentures apparently cause no way. I am also prone to infections after getting a bad one in 6th grade; ear, nasal, bronchitis, kidney, UTIs, mainly. I had surgery on my right ankle three years ago and he cut a nerve during it that did not heal so the top of my 4th toe and half of each next to it have no feeling. I think that's all. Nothing too weird I don't think. lol
 
I have now been diagnosed with autoimmune thyroiditis. So there was a reason for my increased fatigue, slow metabolism and excess weight. Now I have to undergo lifelong hormone therapy. But you can live with it.

I am glad you got our diagnosis because that is the first step to feeling better.

Thyroid stuff is hard because of how much it impacts, but fortunately most thyroid things can be treated and you can live with it. May sounds a little nuts, but I am thankful I had thyroid cancer and not something else. Even if my treatment did not goes as it should since I did not uptake the radioactive iodine, I have been living a good life with it for the last 19 years. Sure there are struggles, weight being one, but we all have our struggles, right?

I hope your therapy helps you feel better soon. I think I said it before, but chronic illness are not fun, but with the right treatment they are totally doable.
 
This is so interesting to me. I'm missing a chromosone that makes me wake up from certain anestesia. We found this out when I took 45 minutes to wake up from getting my tonsils out when I was in college; they made me wear a med alert bracelet after that because it was so dangerous. Fortunately, I've never had any issues with it since, but the doctor said if I was exposed to that drug again, I might not wake up!

Okay, that not waking up from anestesia is really scary! I wake up from it puking, first time right on my poor sister, but I wake up pretty fast. After that first time, they started putting something in my IV to help with that, so it is not a huge problem, but that first time. Man, it was intense. Like I said, my poor sister. Still feel bad about that and it was over 20 years ago.

It's amazing what we don't know about ourselves until something like surgery or an accident happens. Besides not knowing about the puking or the dissolvable stitches, I found out I was allergic to adhesives then too. They put a strong adhesive bandage over the surgery scar on my neck and it was killing me. When they took it off to see what the issue was, they took off layers of skin with it. I ended up with a bigger issue with that then the scar, it was so bad.

Shoot, after writing that, it is really apparent how atypical I am. :blink: I am also allergic to latex. LOL
 
I have naturally low blood pressure. When I am at a healthier weight, it's low enough to make me get light-headed and dizzy often. There's also some extra bone on the inside bottom of my mouth. It makes dental work more difficult but doesn't affect me normally. The dentist mentioned to me recently that if I have to get dentures, they would have to cut that bone out! I will never get dentures apparently cause no way. I am also prone to infections after getting a bad one in 6th grade; ear, nasal, bronchitis, kidney, UTIs, mainly. I had surgery on my right ankle three years ago and he cut a nerve during it that did not heal so the top of my 4th toe and half of each next to it have no feeling. I think that's all. Nothing too weird I don't think. lol

Wow on the extra bone! I would definitely avoid the denture route too! Just the thought of cutting out a bone gives me the willies.

The infection thing is the same for me and was for my mom. She almost died of septis from a UTI and after that, any infection she got hit her hard and made her crazy. No lie, she would get outta her head with it and get violent. When she was in full blown dementia it could get ugly. At the end, she thought I was her mom, so I usually got her to calm down, but she gave me some bumps and bruises on the way. Dementia is so horrible.

Does the toe bother you much? I know when my feet fall asleep, if I try to stand up, I am going to fall on my face. That is probably an extreme version other than a toe and half of two others, but balance is balance.
 
Wow on the extra bone! I would definitely avoid the denture route too! Just the thought of cutting out a bone gives me the willies.

The infection thing is the same for me and was for my mom. She almost died of septis from a UTI and after that, any infection she got hit her hard and made her crazy. No lie, she would get outta her head with it and get violent. When she was in full blown dementia it could get ugly. At the end, she thought I was her mom, so I usually got her to calm down, but she gave me some bumps and bruises on the way. Dementia is so horrible.

Does the toe bother you much? I know when my feet fall asleep, if I try to stand up, I am going to fall on my face. That is probably an extreme version other than a toe and half of two others, but balance is balance.

My grandma passed last summer after a few years of dealing with dementia. It really is horrible. My brother-in-law works in a nursing home and said there is some sort of connection with dementia and UTIs. I've had lots of bad infections, but three years ago I wound up in the ER when a severe kidney infection hit me with no warning. I had to be taken from work in an ambulance and was given fentanyl. It was intense.

The toe bothered me a lot at first. Every single thing that touched it was so painful, the sheets on the bed killed me. Now the nerve pain isn't nearly as bad as all, more irritating than anything.
 
As far as I know, slightly lower than average temperature seems to be it for me. We sure are all unique, aren't we! Everything else but the temperature, I blame on weight and back issues and a foot I really badly broke in my 40's.
 
My grandma passed last summer after a few years of dealing with dementia. It really is horrible. My brother-in-law works in a nursing home and said there is some sort of connection with dementia and UTIs. I've had lots of bad infections, but three years ago I wound up in the ER when a severe kidney infection hit me with no warning. I had to be taken from work in an ambulance and was given fentanyl. It was intense.

The toe bothered me a lot at first. Every single thing that touched it was so painful, the sheets on the bed killed me. Now the nerve pain isn't nearly as bad as all, more irritating than anything.

I am sorry about your grandma. UTI's definitely made the dementia worse in my mom's case, so I would believe there is a connection. I believe an infection can happen that fast, with no warning, and it can be painful and scary. Is a kidney infection as bad as a kidney stone? Kidney stones suck.

It is incredible how much sheets can hurt. I have a bone spur on my heel that I can't allow to touch the sheets because of the pain. I sleep with my leg bent and crossed over the other one so that heel never touches the sheets. The dang spur is wrapped around my Achilles tendon so I would need major surgery to get rid of it, so I just deal and sleep like a pretzel. But Tracey M is right, since I have lost weight the bone spur does not hurt as much. Except at night on the sheets. LOL
 
As far as I know, slightly lower than average temperature seems to be it for me. We sure are all unique, aren't we! Everything else but the temperature, I blame on weight and back issues and a foot I really badly broke in my 40's.

Weight is a big contributor to a lot of my aches and pains too. Since I've lost some, my back does not hurt as much, which is great. I think back pain is the worst.

We are all definitely unique and that is what makes it fun and interesting. :)
 
I am sorry about your grandma. UTI's definitely made the dementia worse in my mom's case, so I would believe there is a connection. I believe an infection can happen that fast, with no warning, and it can be painful and scary. Is a kidney infection as bad as a kidney stone? Kidney stones suck.

It is incredible how much sheets can hurt. I have a bone spur on my heel that I can't allow to touch the sheets because of the pain. I sleep with my leg bent and crossed over the other one so that heel never touches the sheets. The dang spur is wrapped around my Achilles tendon so I would need major surgery to get rid of it, so I just deal and sleep like a pretzel. But Tracey M is right, since I have lost weight the bone spur does not hurt as much. Except at night on the sheets. LOL

My husband just got done dealing with kidney stones for the last month. It was terrible. We brought him to the ER 3 times, he had 3 surgeries, and he spent 3 overnight in the hospital. I would say the pain was probably equal to my kidney infection, but the difference was, I could fix mine with just a couple of rounds of strong antibiotics. I didn't need all the other stuff my husband needed and dealt with.

I sleep a little weird now, too. I cannot make that ankle go straight, so I tend to just bend at the hip. Not quite as pretzel as you, but not the way I used it. The not bending properly affects me the worse when doing yoga though. I cannot do some moves anymore and it's frustrating, but the surgery was still worth it.
 
I sleep a little weird now, too. I cannot make that ankle go straight, so I tend to just bend at the hip. Not quite as pretzel as you, but not the way I used it. The not bending properly affects me the worse when doing yoga though. I cannot do some moves anymore and it's frustrating, but the surgery was still worth it.

Life is totally about adapting to the new things, both good and bad, isn't it? Luckily the human race is really good at adapting. ;)
 
Oh boy do I have a plethora to share lol. Most of my issues may not seem strange in the "atypical" sense, but to have all these issues at once and at my age (I'm not even 35 yet and I've had these issues since I was 25, or starting around that time) something unusual has to be going on.

So first of all, pre-dating all the other issues, I was diagnosed with TMJD (temporomandibular joint disorder) in 2008. Essentially it's arthritis in the jaw bone, although there is more to it than that that's the best way to describe it. There's little cushioning left where my jaw bone meets my skull (up near the ear, which is why it can sometimes present like an ear infection) I can no longer eat certain things like steak because of how hard it is to chew, I can no longer chew gum or certain types of candy (I haven't had a Starburst or any kind of taffy for over 10 years, blah). What truly sucks is that it totally changes your eating habits, and it's made me self-conscious about HOW I eat, so I don't like to eat in sit-down restaurants anymore. For example, I don't like to open my jaw wide anymore, so the result is eating things like burgers with a fork (or tearing off pieces). Pizza, burritos, even Subway sandwiches too. People don't understand that it hurts and that it's a condition, so the strange and honestly judgmental looks from people aren't worth it, so we stick with takeout or I eat at places with items that people won't judge me for using a fork (buffets are great - you know, once the plague is over lol).

Also, somewhere along the way I was diagnosed with agoraphobia and severe anxiety disorder with associated panic disorder (I have panic attacks).

Then around 2013 I started having my "health crisis". I have a laundry list of symptoms. I started having tremors, my hands were constantly shaking when I felt normal. I noticed it when I would knit, crochet, and cross stitch (which relax me, so why would it be my anxiety to blame). I started feeling weak, feeling like I'd literally run a 10K when all I did was put a load of laundry in - out of breath, shaky, cold and clammy with sweat, and lightheaded. Then the fainting episodes started - one morning my husband and I had a lazy moment in bed for 20-30 minutes but I eventually had to get up to go to the bathroom, and I'd used the bathroom and walked all the way back to the dresser in my bedroom to get dressed, feeling fine, before I dropped like a stone to the floor. Fainted dead away. Like I said, I had been upright for a good minute or two already, so it wasn't "oh man I got up too quickly". I only gained more symptoms to add to the list - random skin rashes (that they "ruled out" as Lupus), muscle jerks (I quit driving after the time I was at a stop light and had a sudden muscle jerk that almost made me slam the gas with another car stopped in front of me), and people told me that they noticed I suddenly got more "clumsy" and stumbled over myself more often but also started to noticeably lean when I stood. There was a lot more but it's just so much. I went to a couple of doctors, touted to be some of the best in this state, but...well, the GP told me he suspected Lupus and referred me to an endocrinologist, the endocrinologist told me I probably had rosacea and was letting my anxiety get the best of me and to see a psychiatrist, the psychiatrist told me she thought I had a physical issue and to go see a neurologist, and the neurologist must have forgotten that her specialty was generally in the head area because she thought I had a gastrointestinal disorder (that I had no symptoms of). They were all taking me for a ride, I had started to rack up some serious bills because I'd had multiple tests including an MRI that I had insisted on (i.e. probably not covered by insurance), and these doctors just kept passing the buck. I stopped the search after that. I was being treated during that whole time, by the way, by my therapist for my anxiety, and my physical symptoms continued.

It wasn't until a couple years later...I went to a family doctor because my back always hurt. The "laying supine on the couch crying" kind of hurt. I had been told by the original GP (that suspected Lupus), who had actually run a boatload of tests back then including an x-ray of my back and neck, that I had several discs in my back and C-spine that were pinched and/or had degeneration. The second GP diagnosed me with severe arthritis and after hearing about my other issues, diagnosed me with fibromyalgia.

And that has been my struggle ever since. I still suspect that the fibromyalgia may either be a misdiagnosis or that I may have fibro but also something else, because fibro doesn't explain a lot of things. Chronic illnesses like to gather - I have met so many "spoonies" (chronic illness sufferers) that have 2-3 different, unrelated diagnoses. In fact, I have honestly never met one that only has one. I still struggle with tremors and shakes sometimes. I now have arthritis in other areas - mildly in my knees, my legs sometimes hurt, and I now struggle a lot with sciatica and pinched nerves in my hips (mostly my right), down my legs, and a lot in my back. 7/10 nights I spend tossing and turning because one or the other hand/arm will go totally numb, usually the arm I'm NOT laying on, because of all the nerves in my back that pinch. Those issues flare up a lot when bad weather comes through - which we actually have a storm blowing in over the next 24 hours so I'm having these issues now.

As far as diagnoses, I have none for the unresolved issues like the fainting and tremors. The rashes have mostly gone away but sometimes one still crops up, and in the last 5 years I've had bouts of breaking out into hives for no reason, at least twice - the last time was right after we moved, October or November. Again, no reasonable explanation. I have also developed chronic migraines (lovely), though thankfully compared to how I know migraines can be for some mine are mostly mild with the occasional very-not-mild one. I'm fairly certain it's not Lupus like original GP suspected. It's definitely not the gastrointestinal disorder the neuro suspected - I actually now have a FB friend with exactly that disorder and I don't have the same issue as she does, at least with her gastro disorder. I have always suspected a disorder called POTS (postural orthostatic tachycardia syndrome), it causes raised heart rates (my RESTING is in the mid 90s bordering on 100s, and can jump to the 120s, that ain't normal) and fainting. I've also suspected it could be caused by thyroid issues, but things don't all quite "fit into place" with that one like it does POTS.

However, as of today, other than my arthritis, TMJ, anxiety, and fibro, I remain undiagnosed for the weird issues. After all that I went through before, I'm not rushing to see more doctors just to get a diagnosis. I have learned to live with my issues, the only thing that is hard to live with is the chronic pain but since I do not want to go back on painkillers there's not much a doctor can do for me that I don't know and can't do myself (exercise, rest, homeopathic remedies, etc).

So...yeah, I have health weirdness. Definitely. lol
 
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