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Permalink Reply by Jessica Ables on February 7, 2011 at 5:22pm Ben, I have sent emils to hospitals in the past with questions and concerns. I've found though that I get quicker and better responses with a phone call and the follow up is also better when speaking to an actual person. I hope this helps and I would definitely recommend sending the medical records first or at least faxing them a copy of a summary of your condition. This is how I first got into UCLA. My neurosurgeon had emailed all of my scans and records to the "referral" line. This was a year ago and I've yet to receive a response from that line. I'm thinking it was because they probably receive so many. After having waited a week, I went online and got the exact phone number of the doctor and he contacted me back within 48 hours, had me send him my scans on a CD, and got me in for a consult two weeks from the time of initial contact. Within two months I'd had new scans done, been fitted for my SRS mask and my actual treatments scheduled. This was back in June 2010 I hope this helps and I wish you the best. I'd also like to say that by mentioning above that my referral hadn't been answered by UCLA in no way speaks of their service. I know that the line my info went to first probably gets filled with other referrals and patient records that it takes a lengthy amount of time to get to them. Their care and service has been excellent, it just helps to have them put a face or voice to the records they have in front of them.
Best to you,
Jessica
Permalink Reply by Brett D on February 7, 2011 at 9:48pm Hey Ben,
When I was getting second third fourth opinions etc only one of them answered questions via email. However I did have a prior appointment with him that he had to cut short as he had an emergency to attend. Maybe he did this to make up for the short time I had with him.
I posed a question Here in the weekend and got a reply with in a few minutes. I got a quick answer but he stated he could not give me an accurate answer without knowing my records in detail and he suggested I schedule a consultation with his office. I'm in California so I didn't want to waste his time. He was very accommodating however.
wHAT STATES ARE YOU CLOSE TO? WENT TO JEFFERSON WITH MY SON, NOT IMPRESSED WITH DR. ROSSENWASSER, FROM JEFFERSON. IF YOU WANT TO KNOW WHY FRIEND ME. I CAN'T STRESS THE IMPORTANCE OF MULTIPLE OPINIONS WE GOT SUCH DRASTIC DIFFERENCES IN MY SONS PLAN OF CARE FOR RESIDUAL AVM, THANK GOD I SEARCHED OUT OF THE PHILADELPHIA REGION AND FORTUNATE TO HAVE INSURANCE THAT ALLOWED US TO DO SO. i DO BELIEVE THAT THE NEURO MD NEEDS TO VIEW YOUR SCANS TO COME UP WITH A PLAN. ESPECIALLY WHEN DEALING WITH AVMS SINCE NO 2 ARE ALIKE. ALL THE BEST TO YOU.
Permalink Reply by Ben Morrell on February 7, 2011 at 10:13pm Thank you everyone for you comments and suggestions.
I did go ahead and sent an email to a doctor/hospital that's only 50 miles away from where I live. It's a research and teaching hospital with a good reputation. Now, I'll wait and see if they reply back.
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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…
ContinueOctober 11, 2011 at 6pm to October 10, 2012 at 7pm – Some where with good Coffee
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