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Permalink Reply by lakersfan86 on February 19, 2012 at 1:52pm My advise before you go for extra diagnostic procedure:
Show the existing suspicious imagery to another doctor and ask them what to do. If they also say angiography, have one done.
Since the 'other radiologist' seems to suspect something vascular, maybe look for a person from the field.
what is the suspicion btw ?
Permalink Reply by Tricia on February 28, 2012 at 12:00am Yes I agree with the above Kristina Angio is the way to go, far better results than MRI, good luck
I have had countless MRA's for checkups it's easy and relatively non-invasive (They do inject you with a dye). The angiogram is the easiest way to do a check up but requires some recovery time and in my opinion is annoying. I often only get them with my embolizations.
Permalink Reply by Ed B on March 30, 2012 at 4:34pm Hello all, where are you located? It will only confirm what the MRI had shown.
MRI's are OK if there aren't any Metle Clips in the area that was treated. If there is, let the people at the check-in desk know. They may kick you out of the Building!!!!!
Permalink Reply by RoxAnne Parker on April 3, 2012 at 2:54pm Ive had 4 angiograms and they can see better on what is going on. It ok :)
Permalink Reply by Amy (the worrywart) on April 10, 2012 at 12:44pm I am scheduled for an diagnostic ANGIO this coming Thursday as well as an MRI next week. My doctor wants to look at both. He said that the MRI is like looking at still shots while the ANGIO is like looking at a motion picture.
Hi,I had six or seven angiograms...it is easier to see what is in there. In my case, it helped.
Permalink Reply by Lori Gibson on April 16, 2012 at 9:27am Do you still have an AVM? If so did it bleed? I was having problems associated with my AVM two years before it actually burst. I had headaches all of the time, and got vertigo a lot. I started out with an ear,nose, and throat Dr, because they thought that I might have Meiniers disease. After about a year of testing, I then was referred to a Neurologist. He then started running tests, Cat-scans, then a MRI. The MRI did not show that I had a small AVM in the back of my brain. So needless to say, He diagnosed me with "Atypical Migraines" he sent me on my way telling me I would have to just live with it. Well, eventually my AVM burst... I was rushed to the hospital. I was in a coma for about two weeks, I was in intensive care at that hospital for 8 weeks. I was then transferred to a rehab hospital. My AVM was inoperable at that time. I was then referred for Gamma Knife surgery, which I had done. The Ironic thing is, prior to the Gamma Knife the Neuro Surgeon ordered a MRA, They used the MRA to map my brain for the surgery. So, in the long run, had my previous Neurologist ordered an MRA versus the MRI they would have seen my AVM, and I would have had the Gamma Knife prior to my bleed and would have avioded my Near-Death bleed.
Oh. They also did an AngioGram one year after my Gamma Knife surgery.
Permalink Reply by Brooke on April 19, 2012 at 12:22am This community is part of the Ben's Friends network of patient communities. Learn more at bensfriends.org.
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Posted by Sam on May 27, 2012 at 3:30pm 0 Comments 0 Likes
I'm counting down the days!!! At the end of June 2012 i have to go to the hospital for another Angio.
Hope to hear good news, that the Embolization and 2 Gamma Knife treatments where succesfull and that after 7 years of fighting the AVM is…
Posted by kristi on May 26, 2012 at 3:17pm 3 Comments 0 Likes
I had a bruit when I had the AVM. It was there all my life. I guess everyone hears it at some point but as an "AVMer" mine was ALWAYS present. We became friends:)
My bruit was my connection to my heart, so I always thought (when I never…
Posted by stephanie on May 26, 2012 at 1:24pm 4 Comments 0 Likes
Click here to visit my latest blog post. If anyone could shed some light on the conclusiveness of MRI and angio, it would be great! The surgeon…
ContinuePosted by existentialmom on May 25, 2012 at 4:48pm 2 Comments 0 Likes
Merlin came through the first gamma knife well, and we are scheduling stage 2 in August. Her treatment time was 152 minutes! No side effects yet.
We are relieved, but holding our breath against the next 3 months, 6 months, 1 year, 3 years,…
ContinuePosted by Cat D on May 25, 2012 at 3:14pm 2 Comments 2 Likes
I only got accepted to this site yesterday and already I feel at home. I hope that this will be good for me and my mom who also was accepted yesterday. We both have been through a lot in the…
ContinuePosted by Ben Munoz on May 25, 2012 at 9:14am 0 Comments 2 Likes
Dear Friends and Family of AVMSurvivors,
We are so excited we cannot wait to tell you about how our organization is growing, so we’ll go straight at it. We are please to tell you that collectively our patient…
ContinuePosted by DsSis on May 25, 2012 at 12:37am 5 Comments 2 Likes
David's surgery was May 14th and today, May 24th, we had a series of wonderful things happen.
1) I finally got to see my brother walk (with the assistance of his wonderful physio) - he made two rounds of the hospital ward...I was the last…
Posted by Hiro on May 23, 2012 at 8:50pm 10 Comments 0 Likes
I had the neurologist appointment on Monday, and he diagnosed me with "Executive Dysfunction Syndrome" that he thinks stemmed from some sort of damage to my left frontal lobe during/after my surgery (that was where my 3 AVMs were), contributing…
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