Accident à la sortie du pont Pierre-Laporte direction Lévis.

Vers 23 h 20 le 14 août, à la sortie du pont Pierre-Laporte en direction de Lévis, un important accident impliquant plusieurs véhicules venait de se produire. Des automobilistes se sont arrêtés et certaines personnes sont sorties de leur véhicule afin de porter assistance aux personnes impliquées.

Alors que des témoins s'approchaient de la scène, deux coups de feu ont été entendus à proximité de la camionnette accidentée. Au départ, certaines personnes ont cru qu'il pouvait s'agir d'un pneu qui éclatait. La situation est devenue plus claire lorsque des automobilistes ont brusquement reculé et que plusieurs personnes se sont mises à courir en signalant la présence d'une arme à feu.

Les témoins se sont alors éloignés rapidement de la scène.

Une importante intervention policière a ensuite été déployée. Le Service de police de la Ville de Lévis, la Sûreté du Québec et le Service de police de la Ville de Québec étaient notamment présents, ainsi que les services incendie et ambulanciers. Le secteur de l'autoroute a été fermé pendant l'intervention et l'enquête.

Les circonstances exactes entourant l'accident et les coups de feu demeuraient à déterminer au moment des événements.

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u/Marylee555 — 5 days ago

Severe recurrent left-sided pelvic/lower abdominal pain, but ultrasound and CT were normalany ideas?

36F. A few days ago, I suddenly developed extremely severe pain in my lower left abdomen/pelvic area. It felt very deep, around where I would describe my left ovary being. At its worst, it genuinely felt like something was tearing/ripping my insides out. The extreme pain lasted around an hour and then gradually improved significantly, although some pain remained.

I also had bright red vaginal bleeding at the same time and it stopped hours later. I had a NovaSure endometrial ablation about a year and a half ago. Since then, I can still have some spotting around the time of my period, but this was more clearly bright red blood than what I usually see.

I went to the ER. They did a pelvic exam and told me the blood appeared to be coming through/from the cervix. I then had a pelvic/transvaginal ultrasound. Both ovaries looked normal and they found no ovarian cyst or obvious torsion.

Because of how severe the pain had been, they also did a non-contrast CT/urogram to look for kidney/ureter stones and other possible causes. That was also reportedly normal. My bloodwork did not show significant inflammation. I was eventually discharged with the possibility that the pain might be musculoskeletal.

The problem is that three days later, I'm having another acute episode of the same type of pain.

Medications:

Levothyroxine, Bupropion, Sertraline

Regular PRN : propanolol(extrasystoles), zopiclone and melatonin.

Relevant history:

NovaSure endometrial ablation approximately one year ago

Tubal ligation

Two previous C-sections

PCOS

Recurrent pelvic/uterine cramping and intermittent spotting since the ablation

My gynecologist and I have already been discussing further treatment, potentially including hysterectomy

I'm confused because the pain can be absolutely excruciating, yet the ultrasound, CT and bloodwork didn't show an explanation. They said it could not be a torsion cause there's no cyst on my ovaries.

Thanks

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u/Marylee555 — 6 days ago

Severe recurrent left-sided pelvic/lower abdominal pain, but ultrasound and CT were normal

36F. A few days ago, I suddenly developed extremely severe pain in my lower left abdomen/pelvic area. It felt very deep, around where I would describe my left ovary being. At its worst, it genuinely felt like something was tearing/ripping my insides out. The extreme pain lasted around an hour and then gradually improved significantly, although some pain remained.

I also had bright red vaginal bleeding at the same time and it stopped hours later. I had a NovaSure endometrial ablation about a year and a half ago. Since then, I can still have some spotting around the time of my period, but this was more clearly bright red blood than what I usually see.

I went to the ER. They did a pelvic exam and told me the blood appeared to be coming through/from the cervix. I then had a pelvic/transvaginal ultrasound. Both ovaries looked normal and they found no ovarian cyst or obvious torsion.

Because of how severe the pain had been, they also did a non-contrast CT/urogram to look for kidney/ureter stones and other possible causes. That was also reportedly normal. My bloodwork did not show significant inflammation. I was eventually discharged with the possibility that the pain might be musculoskeletal.

The problem is that three days later, I'm having another acute episode of the same type of pain.

Medications:

Levothyroxine, Bupropion, Sertraline

Regular PRN : propanolol(extrasystoles), zopiclone and melatonin.

Relevant history:

NovaSure endometrial ablation approximately one year ago

Tubal ligation

Two previous C-sections

PCOS

Recurrent pelvic/uterine cramping and intermittent spotting since the ablation

My gynecologist and I have already been discussing further treatment, potentially including hysterectomy

I'm confused because the pain can be absolutely excruciating, yet the ultrasound, CT and bloodwork didn't show an explanation. They said it could not be a torsion cause there's no cyst on my ovaries.

Thanks

reddit.com
u/Marylee555 — 6 days ago

Did you guys had the diagnosis at the beginning?

I have hypothyroidism since I'm 12. I had a very large thyroid. Went on synthroid since then.

Now I work at a hospital and someone told me if I had a very large thyroid and hypothyroidism at that age, its hashimotos. But no doctor told me that before. Like we we're only checking for my thyroid level and that's it.

I'm now at 175mcg of synthroid. I've always had up and down.

I have neurological symptoms that look like ms and I'm getting investigated for that. I know if you have a autoimmune disease you are at more risk for other one.

My question is, is it possible that they don't always put the word hashimotos and just treat the thyroid level, but you have it? Like they don't go check for it cause anyways they will treat it with synthroid? I just wanna know if it happened to someone else. Thanks

Sorry for ny bad english.

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u/Marylee555 — 3 months ago