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well my pt actually gave me a posture shirt to try out, it's much tighter which is good
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yup its awesome but if you take too much magnesium you have to be careful because your diaphgram relaxes too much and you start hyperventilating |
thanks ill look into medrol/taradol. i just assuemd it was like lyrica which i do NOT agree with taking.
so another question!! if i had a c-spine mri would it say if i have a big?? transverse process? because my pt said i have this. i need to read up more on bones. so far i've been obsessed with shoulder anatomy and nerves. |
No, a c-spine MRI will not show an enlarged transverse process. Due to me showing significant arterial problems and having had an abnormal 1st rib removed already, my doctors ordered a specific x-ray to look at the transverse process. He said the test that will really show the size is a CT scan of the neck. I already had a CT scan done for another reason so the doctors reviewed the scan and x-ray. Yep, I've got a hypertrophed transverse process.
Personally, I wouldn't request a CT scan due to the radiation exposure unless there were other signs leaning towards a potential issue with C7. |
thanks so much, ive been worrying about this quite a bit. so i will request an x-ray no ct scans.........
do you know if surgery (?) to fix an enlarged transverse process is as invasive as say...a rib ressection? i have ehlers danlos syndrome and im terrified of scar tissue. i'm a worry wort after all the stress i've been through. i feel like mentally i have to juggle in my head each day how much my physical therapy for winged scapulas is working for me. |
i dont see much info on transverse surgery, most of it's on fractures. i wonder if it's really that rare
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so i'm going in for an appointment next week. ill ask about those drugs and if she thinks theyre appropriate, since my sx are more muscular i bet they'll hesitate to give me them.
i'm also wondering if i should just go ahead and get an mri of my bp. i never requested one because ive heard theyre usually pointless |
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It wasn't until I stopped PT, rested, and got aggressive with getting rid of myofacial trigger points (massage therapy, anti-inflammatory drugs and home ultrasound/TENS combo therapy) that the neurogenic and vascular TOS symptoms became obviously apparent. We have a pain bucket, and when that bucket is full and overflowing you really only feel the most noticeable pains (at least that is how I am). |
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