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For medical advise consult your physician.
Dears; The end of migraine surgery,
was done by a simple surgery, that can cure all migraine patients
without any side effects. All are true, and in surgery results talks.
No need to come to me for surgery its a simple surgery, just do a
copy about the surgical treatment page and tell any surgeon you know.
If he has any question I m ready to answer him. All doctors and drugs
in the world cant cure even one migraine patients, because they think
that intracranial arteries also cause migraine headache, in my study
I prove that only extracranial arteries cause migraine headache, while
intracranial cause aura and acompanied symptoms. my abstract entitled
Migraine - New Surgical Treatment - has been accepted for the Oral
Poster Presentation category for the 2001 Congress of Neurological
Surgeons meeting, September 29 - October 4, in San Diego, California.
Abstract Number: 173 ***://155.100.34.97/abstracts/search.html Where
you can find My abstract: ***.neurosurgery.org click on CNS or ***://***.neurosurgery.org/cns/index.asp
click on meetings or ***://***.neurosurgery.org/cns/meetings/index.asp
than click on search abstract archives or ***://155.100.34.97/abstracts/search.html
you can find my abstract in abstracts on 2001 San Diego, California
put in keywords ( migraine) ***://155.100.34.97/abstracts/abstracts.fm
or direct to the abstract: ***://cnshome.org/abstracts/abstracts.fm?value=43363&field=recid&html=detail&doscript
They don’t want you to know about my new surgery, because they care
more about your money. To read about that read this; ***://***.hunterdonhealthcare.org/WebMD/Conditions/Migraine_Headaches/Surgery_Treat_Migraines.asp
Best Wishes
Ali Sultaneh <loverss_AT_gawab_DoT_com>
Damascus, Da - Wednesday, September 24, 2003 at 11:38:29
I don't know where to put this question so am going to try here. My brother had surgery Apr '98 for a meningioma on the L parietal involving the optic nerve, he lost sight in the L eye, the optic nerve is dead. His MRI now shows a 25% growth rate in 6 months. His M was surrounding and part of the carotid artery, they removed what they could and 'cut' off the blood supply to the rest. Now they want to insert a baloon into the L carotid artery, remove it and he can live with one carotid artery? The lymph nodes in his neck are full of 'lumps' so they will be removed prior to the neuro surgery. He is 50 and very active up until now. I really need someone to tell me if you can actually survive with only one carotid.
I would appreciate hearing from anyone
Thank you
Jan
Jan <Brier_Isle_AT_yahoo_DoT_ca>
- Monday, September 15, 2003 at 01:56:25
I have PN. I like to talk to others who have it in order to learn
more about this miserable disease.
Judy Duet <granny_AT_mobiletel_DoT_com>
Galliano, LA - Tuesday, June 17, 2003 at 18:12:01
My mom, Kathy was in ICU Blake for a month and is now coming home
from her second and final surgery and doing very well. Thanks to the
staffs at Blake and Ellison for their outstanding effort and care.
The Corcorans and Sheridans
Tom <Thomas_DoT_corcoran_AT_tfn_DoT_com_DoT_>
Boston, m - Monday, June 16, 2003 at 11:09:59
I am a PGY-1 neurosurgery resident planning to initiate my residency
PGY-2 in neurosurgery at a US program that appears endangered to close.
Does anyone know of any PGY-2 spots available? Sincerely, PGY-1
neurosurgery resident <neurosurgeon7_AT_hotmail_DoT_com>
new york, ny - Thursday, June 5, 2003 at 15:45:19
My 21 year old cousin Vinny suffered a AVM Jan. 14, 2003, He was
in a Coma for 3 1/2 weeks, he has had 2 brain surgeries. He was in
a rehab for 3 months, he will be going back to the original hospital
when medicaid allows his next 45 days of rehab in july. He has come
along way.
Nicole McCormick <nickmick2002_AT_msn_DoT_com>
FL - Wednesday, June 4, 2003 at 20:05:20
well,i just wish wed find a proper cure for cancer soon cause i
lost my *** last yr when i was 17 n i dont want anybody else to go
thru what i did.so i just wish we cud find a cure for cancer soon...
angy <coolanks_AT_sify_DoT_com>
delhi, delhi - Wednesday, June 4, 2003 at 06:44:12
well,i just wish wed find a proper cure for cancer soon cause i
lost my *** last yr when i was 17 n i dont want anybody else to go
thru what i did.so i just wish we cud find a cure for cancer soon...
angy <coolanks_AT_sify_DoT_com>
delhi, delhi - Wednesday, June 4, 2003 at 06:41:19
HELLO, MY LITTLE GIRL HAS DANDY WALKER SYNDROME. SHE WAS BORN AT
38 WKS GESTATIONS BY C-SECTION. SHE HAD NEURAL TUBE DEFECT WITH MENINGOCELE
OCCIPITIAL UPON WHICH WAS CORRECTED 3 DAYS AFTER BIRTH.SHE WAS DIAGNOSED
WITH DANDY WALKER VARIANT. SHE WAS IN BRENNERS CHILDRENS HOSPITAL
IN WAKE FOREST UNIVERSITY /BAPTIST HOSPITAL. THAY WHERE SURPERB WITH
HER THEIR. I AM THANKFUL TO THEM ALL. HER NAME IS GRACIE AND SHE WAS
TOUCHED BY GRACE, BECAUSE SHE IS AS NORMAL AS ANY 6 MONTH OLD BABY.
IF ANY ONE HAS ANY THING THAT MAY BE HELPFUL TO ME ABOUT ANY OF THESE
PROBLEMS.I WOULD BE VERY GRATEFUL THANKS DONNA
MR.AND MRS. RICHARDSON <DR1LOVEDR2_AT_AOL_DoT_COM>
NORTH WILKESBORO, NC - Thursday, May 29, 2003 at 21:06:41
Greetings ~ Have any of you good people out there who are post
op for transphenoidal surgery been diagnosed with Rathke's Cleft cyst
? I am freshly post op and would very much like to communicate with
someone who has been through this. There is significant damage to
my pituitary as well... Thank you for listening. I welcome hearing
from you. I wish you all the very best of health.
Nan Chambers <nchambers@gwi_DOT_com>
Topsham, Maine - Tuesday, April 15, 2003 at 02:10:03
I seen an ENT Doctor yesterday and went for an last minute MRI.
PCP called and I was told I have Meningioma, 2.1cm (size of acorn).
I trust my PCP, and was told not to worry. Could someone enlighten
me about this. I am 66 yrs young.
Linda M. W <libra5owl@webtv_DOT_com>
Pompano Beach, Fl - Tuesday, April 1, 2003 at 16:21:15
I was first diagnosed with Hydrocephalus when I was thirteen years
old.I am now thirty.I have a VP Shunt on the left side of my head
and I have had 4 brain surgeries and 1 surgery on my abdomen to remove
the extention that was disconnected some how.I guess the hardest part
of all this has been the gradual loss of memory.I don't remember what
else bothers me about it.I have a wonderful neurosurgeon in Kansas
City,Ks. at the University of Kansas Medical center.His name is Dr.Steven
B. Wilkinson.He truly is the epitome of a good doctor.I have been
told that there is no cure for Hydrocephalus which translates to:
This is just one of those things I can't do nothing about.I can and
have handed this situation ALL over to God.He has done some awesome
work on me to deal with it. I've learned that in every bad situation
is a good. It's just cleverly disguised as a pebble in my shoe. For
instance, I never see re-runs of most of the television shows and
movies I watch. I can hide my own Easter eggs,I can buy my own Christmas
presents, and I meet "new" people everyday.(we're still looking for
the eggs from Easter of 1994)This all may sound like I'm a little
off my rocker but it has become a wonderful coping mechanism. "If
you can't fix it,laugh at it." And if anyone wants to pay a mere 50cents,
I'll let you put your ear to my head and listen to the waves.For me
it's the 'little things' that amuse me and God that keeps me going.God
loves me so much that He sent His only Son to take my place on the
cross so I could have everlasting life. That my fellow "water-babies"
is worth more than all the earthly treasures in the world.I love God
more than my next breath and I need Him more than that breath.I absolutely
refuse to let satan get any kind of victory in my life. I also know
that when you write a person's name, you are supposed to capitalize
the first letter but, I don't think satan desrves that. I also have
had an Endoscopic third ventriculostomy,obviously, to no avail. I
still needed to have a VP shunt put in.I swear if I ever needed a
kidney,I am blessed by not needing someone else'.But if I did-I could
bet I'd get one from a bed-wetter.(ha!)One time,out of the 5,I had
to be placed on the Oncology unit at the K.U. Med. Center because
the neurology unit was full.I believe God had His hand in this to
remind me not to get so focused on "me" and "mysuffering". The Oncology
unit will humble you in an instant. I'm not saying that I thought
God was punishing me.I just know that as a human, I tend to get so
caught up in "how rough" I have it that I make myself depressed. If
I just completely trust God and put it in His hands He will satisfy
my aching soul. I forget almost everything, so when I do remember,I
thank God for it because it truly is a blessing.I Love God and I'm
not ashamed to say so. When the tide is turning in my head and I feel
so "alone", God is always there.I just have to ask. Not that it's
important,but my e-mail name means: just Have A Little Faith.In my
heart,I believe that faith is blindly reaching for God's hand knowing
that He'll touch your heart with it.The other perk to all these surgeries
is that I can tell "the Jones'es" that I go to the city for a forty-thousand
dollar hair cut and that's a low number guess.Well, I'm sure evrybody
reading this has had their fill of me.I don't want to become like
the turd that wouldn't flush so I'll finish up. This "water on the
brain" thing is just another wedgie in the butt of life.I tell people
who don't understnd that my water pump is shot and Dr. Wilkinson had
to put one in.I just always remember that GOD IS IN CONTROL, not any
of us.God does offer a FREE gift of salvation.You just have to admit
you are a sinner,ask for forgiveness and ask God to come into your
heart.OR, are you 150% sure that if you died right now that you'd
go to Heaven? If so,great! If doubt was on your mind or you had to
think for a second,the answer is probably no.Make that choice now
'cuz you never know.Good luck with dealing with this Hydrocephalus.I
know I'm looking another surgery straight in the eye. I need one but
I don't have any insurance so it will have to wait until it's an absolute
emergency to do anything.Reminds me of the Discover card commercial
where the emergency room doctors are waiting for the guy's credit
card to go through before they "shock" him. I wasn't trying to sound
like a whiner,I just can't get any insurance company to insure me.Once
again, just another wedgie in the butt of life. Well, good luck and
God Bless!
Kammy Reeves <justhalf30@hotmail_DOT_com>
Salina, Ks. - Monday, March 17, 2003 at 21:45:45
my first time to visit this site and so far i think its great.
stephanie <smhughes@core_DOT_com>
newark, oh - Wednesday, March 12, 2003 at 08:04:56
I had a craineotomy in Sept 2002, to remove a large mennigioma.
I have had a complete recovery. I am a facilatator for a new brain
tumor support group and am always looking for new things to bring
to my group to share.
Marianna Hope <garryhope@easlink.ca>
Westville, NS - Thursday, March 6, 2003 at 19:14:08
will like to keep myself updated with latest development in neurosurgery.
vk gupta <vk_neurocare@hotmail_DOT_com>
hisar, haryana - Friday, February 7, 2003 at 10:06:01
I am 25 and very healthy with the notable exception of one potentially
fatal flaw. After experiencing four incidences of mild complex-partial,
seizures, which occurred in roughly three-month intervals, I went
in for an MRI (ironically enough on the Ides of March, 2001), which
revealed a 1 cm (in diameter, I assume) lesion in the upper mesial
region of my left temporal lobe, “appearing to abut the hippocampus,”
as they say. I have been told that it is relatively uniform in texture
and well demarcated. Several doctors have posited that it is a low-grade
glioma, but this hypothesis has not been confirmed by a biopsy. I
am a student of English literature, so, as you can imagine, the location
of the lesion is particularly unfortunate. For this reason, I initially
refused surgery (probably because I did not quite grasp the magnitude
of the risk I was taking) in the hopes that I would at least be able
to earn a Master’s degree, a task that I am three months shy of completing.
Since my initial diagnosis, I have had regular MRIs, and the lesion
has not changed, nor have I had a seizure since beginning a course
of lamictal. My only current symptom, if, indeed, it is related to
the lesion, has been difficulty concentrating, for which I have been
taking adderall (like a hyperactive grade-schooler) with some success.
I was recently given a battery of neuropsychological tests, which
did not indicate any deficiencies in brain function but did confirm
my attention problems, though the doctor administering the tests concluded
that condition is developmental. Of course, other neurologists clearly
scorn data of this sort, and I myself have serious doubts about the
value of the endeavor. An empiricist in the strictest sense, my surgeon
has blithely remarked on several occasions that my hippocampus and
left temporal lobe are probably functioning sorely sub par and that
I am most likely relying heavily on my right hemisphere to get by.
Lengthy descriptions out of the way, here are my questions (also selfishly
lengthy and strictly unempirical): 1. Is there anything nutritional
that can be done to maximize my chances of a full recovery after surgery
(if I have it)? I do not eat meat or dairy, and, though I am not willing
to start eating meat again, I would consider dairy if it would help
reduce brain tissue scarring (here you have the science of a literature
major) or strengthen blood vessels. I do bruise easily. 2. I will
warn you that my doctors laughed at me for this one, but I will ask
it all the same. Is there anything I can do to help train my right
brain to take on a larger role in language-related functions? Typing
with only my left hand? Reading with only one eye? 3. Speaking of
reading, I recently discovered an article by Dr. Tracy Batchelor that
suggested there might be a link between brain tumors and the fluctuations
in hormone levels that occur in pregnancy. If, indeed, this is the
case, could similar hormonal imbalances brought on by other factors
also precipitate tumor growth? I have a particular situation in mind,
but it’s a long story—to be told upon request. 4. Is it significant
that my mother gets migraines and suffered a stroke (as a result of
taking birth control pills), my maternal grandfather died of a stroke,
my grandmother has atypical migraines, my paternal grandfather died
of Parkinson’s, and various types of mental illness have arisen on
both sides of my family tree? Nothing good, I imagine. 5. How much
can the brain recover (or compensate for its deficiencies) in a person
of my age? 6. The last time I had an MRI, one of the doctors (the
surgeon again) gave me what I considered a very grim prognosis: that
the average lifespan of patients with my condition is 5-8 years after
diagnosis. I am almost tempted to submit to my suspicions that the
bronchitis the physician in question (with whom I usually get along
famously) had contracted contributed greatly to the disclosure, since
no one has EVER mentioned anything like this dire before and I don’t
really feel like dying. I think other doctors do not agree, but they
have been skillfully coy. Indeed, I have had to do everything short
of starting a fist fight to get even an admission of uncertainty.
Do you (that is an open “you”) have any insights into the matter (that
is to say, the question of morbidity)? 7. Is there a non-psychosomatic
reason for a heightened sensitivity of smell, taste and touch in a
patient such as myself? Well, enough of this prolixity. If someone
should get through this mess, I would be eternally grateful for any
answers or advice.
LJA <grushenka88@hotmail_DOT_com>
Atlanta, GA - Thursday, January 30, 2003 at 03:15:22
I have some questions on neurlogy i am a student and i want to
do this as a proffesion so can you help me out
Kahtie White <KayStallion@Blackplanet_DOT_com>
Kalamazoo, MI - Monday, January 6, 2003 at 16:34:44 |