Thank you, sounds right. Heard it before but could not remember..nm

• s/l neuro foramina...sm - 2teens
  • neural foramina - C
  • probably neural foramina? - nm
    • Thank you, sounds right. Heard it before but could not remember..nm - 2teens

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Can't

Yes I have, it was performed on my sister Caroline.

I believe this was a part of a step in a whole procedure performed by a team of Swiss doctors flown into Loyola University Chicago in 1981.  Normally a procedure is named after the doctor whom performs the "new" technique, but in the case of a team working on a patient with a chance of high mortality, which does survive.  In late 1979 my sister was diagnosed with hydrocephalus.  She was 16.  The neuron surgeon here in Chicago (more so Arlington Heights, IL) at Northwest Community Hospital consulted with doctors overseas in regards to the procedure as a temporary solution till they reviewed the case.  She was being considered for a new medical treatment for hydrocephalus.  Most children diagnosed with hydrocephalus die at a young age prior to this time as there was no long term treatment.  Those who developed this later on, mostly in their teens is a result of growth spurs from puberty, or a tumor located on or near the Cerebral Aqueduct (of Sylvius).  This is what my sister’s condition was.  The tumor was slow growing, and located above the pituitary gland and near the Cerebral Aqueduct (of Sylvius).  The Doctor not understanding the procedure totally as explained in the overseas phone consult, mis-preformed the procedure.  Instead of entering the skull from the occipital (rear), he entered from the right side of the brain.  No noticeable damage at the time was done.  However, on April 1st, 1981, my sister after having a shunt implanted in her brain by the same doctor, whom performed her first surgery to relieve the pressure on the brain, had a stroke.  This now cause alarm as we believed she was out of danger.  She was rushed to Loyola University Chicago, where after extensive testing and numerous doctors overseeing her condition, they consulted with the doctors whom where developing the Cerebral Shunt for hydrocephalus.  The team from Switzerland were flown in and looked over all the tests and scans at that time, and in about 15 minutes or so, they say the problem was, a tumor in the previously mentioned spot.  The tumor was missed by my sister’s first doctor.  He also in his notes on the first surgery stated his entry point (on the right side of the skull) and that there was no blood in the cerebral fluid when drained to relieve pressure.  Although, the latest scans from when she was recently admitted, showed damage in the area of the entry point on the right side of the brain, a blood clot.  Not to mention, the shunt was laid on top of the tumor.  In all the doctors from Switzerland removed the tumor, corrected the position of the shunt, and reinserted the drainage tube from the shunt that had also become wrapped around my sister appendix the previous November which caused her to have Appendicitis.  For 2 years our family went thru hell from 1 bad doctor who most like was better off in a butcher shop.  I remember all this as I was young and my parents, mostly my mother, kept me around since it was the only way I was able to see her and my sister and father.  My memory, and I paraphrase what was said when my sister was released, that they (the doctors from Switzerland) would work on making sure that in the future, the procedure for relieving pressure on the brain from cerebral fluid would be understood clearly that the entry point would be from the rear, and in between the left and right lobes of the brain.  To my surprise, when I was online and looking up my family’s name, that the Kocher’s Point was the exact procedure that was to be made clear for other doctor’s.

In the end, The Doctor was sued, and lost his medical license, and ordered by the court not to pursue a career in the medical field and was barred from and contact from a position he would dispense any and all medical assistance.  My sister is still alive went to college, got married and has had 5 children even though she was advised to never have children due to the radiation treatment for the cancer/tumor, and the pressure on the shunt from labor.  In years past she has shown that her short term memory is weak and sometimes forgets things if she does not repeat what is said to her.  She is now in 2009, 46 years old.

Could one of these S3s be F3? or something with a similar s/l? I can't document F3 though. New doc, but clearly states above.

Thanks for any help.

xx

ACE inhibitor stands for Angiotensin-Converting Enzyme

and

Ace is the name of a bandage.

I've been wracking my brain all morning since you asked this - my friend, not accessible at the moment, has this type of cancer...it is something I had never heard of before which is WHY I cannot currently remember.....sounds like cerrocellular or something like that - it's a definite C she told me and not serocellular.....but I'm not spelling it right.  So sorry, wish I could have helped.

I'm going to see her later - will get back on this...but it's too late for your MT work, I am sure :(

I like using the first two letters of each word in word pairs, like refa = respiratory failure. If I have other word pairs that have the same letters, I add the last letter twice (or more), like refaa = renal failure. If there was a third word pair, it would be refaaa. This would not work for some people, but it's very fast for me. I also double the last letter when the shortcut would be a real word otherwise, like poree (instead of pore) for posterior region. With this system (and looking at your cheat window at the bottom), you can keep adding on other phrases. If I use acfr for acute fracture, I might use acfrd for acute fracture or dislocation.

That's my main trick, but there are lots others I use. I do add individual words to my expander (especially long words) with no shortcuts so I can start to type and find the word in my screen to just plop the rest in automatically (sorta like how AutoText works).

A lot of what makes sense to you will not make sense to someone else. You just need to find what works for you. Keep trying things out because it can't hurt to keep adding or changing. Not even one day goes by without me adding lots of new entries. The key is to always be looking for ways to type fewer strokes.