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Re: EMG&Myleogram reports:FUSION NOW SCHEDULED

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--

Know that all my thoughts and prayers are heading your way. I will be thinking

of you on Sept 9, praying that all goes well.

Rest and take care,

Love, Patti

EMG&Myleogram reports:FUSION NOW SCHEDULED

I am using the laptop on a tray, but even that hurts so cannot be on the

computer long. My recent cervical myleogram, CT scan, and EMG (nerve

conduction test on my upper body) were all abnormal. All indicated " remarkable "

and " significant " abnormalities at c 3-4 and c-6-7 as well as he congenital

narrowing of my spinal column from c-3 to t-1 (that part can't be changed nor

corrected). Disc bulging and vertebrae degeneration at those locations

posterially, anterially, and bilaterally. Pinched nerves particularly

significant at c-6-7 causing pain, numbness, and tingling to constantly run down

my right arm and outer two digits on my right hand. Pinched nerves and disc and

vertebrae abnormalities also causing significant pain on the right shoulder (as

well as significant muscle spasming and pain), base of my skull in back, upper

back on right side, and in front on and between both collar bones. Not a pretty

picture.

My long term and VERY TRUSTED orthopedic surgeon, Dr. Craig Callewart, has

strongly recommended an extension of my 1999 cervical fusion at c-6-7, which has

beeb scheduled for Sept. 9, 2004 at Baylor Dallas (EXCELLENT hospital). Dr.

Callewart told me that he and some of his colleagues are currently trying to

perfect some " higher tech " artificial discs, but " have only implanted approx 60

in patients so far " . Therefore, he wants to " improve them " and does NOT want to

implant any in me at this time due to all of my other medical issues,

particularly my Ehlers-Danlos Syndrome. He stressed that IM will undoubtedly

require another cervical fusion at c-3-4, but as that area is not as urgently in

need of surgical intervention, he wants to try to wait another 9=12 months so as

not to put my body through quite as much trauma all at once AND in his goal/hope

of better perfecting the artificial discs to implant in me at that area at that

time.

Dr. Callewart was, as always, forthright, direct, and very frank with both me

and my immediate family (all of whom were present) about the surgical risks for

me, including but not limited to: stroke, paralysis, decreased neck mobility,

increased and/or the same level of very high chronic pain level, and death. He

specifically asked to be certain that I have a current Directive to Physicians

and a Living Will. I do. He said that he was reasonably certain that I will be

in a high level of chronic pain and require pain management and pain meds for

the rest of my life. He further explained in detail that he will go in through

the 1999 anterior incision site, how long he anticipates the surgery to last

(pending whether he sees with his eyes and feels with his hands more damage

like he did in 1999), that I will be hospitalized a MINIMUM of 2 days and

nights, that I will be very incapacitated for a MINIMUM of one month afterwards,

that during that time I will require A LOT of assistance with self-help

(bathing, using the toilet, having meals prepared and served to me (and possibly

even fed to me for awhile), that I will be unable to drive during recuperation

(and possibly permently due to decreased neck mobility), that he may recommend

home health care (and will assist me in dealing with my ins regarding that) and

even possibly me going to a skilled nursing facility during the first and most

difficult part pf my recuperation period (due to my multiple medical problems,

slow healing history, etc).

I told him that I trust him with my life and whole heart, that I KNOW he is

not just my doctor but my FRIEND, and that if success is possible, he will

succeed....and if he doesn't, it won't be his fault. He smiled and verbally

assured me that all of this is VERY TRUE. And so now, I await the c-spine

fusion on Sept. 9 (earlier if they happen to have a cancellation, which they

sometimes do). I must rest now. This email has taken a great deal out of me

physically. ALL GOOD THOUGHTS ANA PRAYERS ARE GREATLY WANTED APPRECIATED. I

love each and every one of my " family of choice "

Love,

~LoneStarRose~

(~~)

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Guest guest

--

Know that all my thoughts and prayers are heading your way. I will be thinking

of you on Sept 9, praying that all goes well.

Rest and take care,

Love, Patti

EMG&Myleogram reports:FUSION NOW SCHEDULED

I am using the laptop on a tray, but even that hurts so cannot be on the

computer long. My recent cervical myleogram, CT scan, and EMG (nerve

conduction test on my upper body) were all abnormal. All indicated " remarkable "

and " significant " abnormalities at c 3-4 and c-6-7 as well as he congenital

narrowing of my spinal column from c-3 to t-1 (that part can't be changed nor

corrected). Disc bulging and vertebrae degeneration at those locations

posterially, anterially, and bilaterally. Pinched nerves particularly

significant at c-6-7 causing pain, numbness, and tingling to constantly run down

my right arm and outer two digits on my right hand. Pinched nerves and disc and

vertebrae abnormalities also causing significant pain on the right shoulder (as

well as significant muscle spasming and pain), base of my skull in back, upper

back on right side, and in front on and between both collar bones. Not a pretty

picture.

My long term and VERY TRUSTED orthopedic surgeon, Dr. Craig Callewart, has

strongly recommended an extension of my 1999 cervical fusion at c-6-7, which has

beeb scheduled for Sept. 9, 2004 at Baylor Dallas (EXCELLENT hospital). Dr.

Callewart told me that he and some of his colleagues are currently trying to

perfect some " higher tech " artificial discs, but " have only implanted approx 60

in patients so far " . Therefore, he wants to " improve them " and does NOT want to

implant any in me at this time due to all of my other medical issues,

particularly my Ehlers-Danlos Syndrome. He stressed that IM will undoubtedly

require another cervical fusion at c-3-4, but as that area is not as urgently in

need of surgical intervention, he wants to try to wait another 9=12 months so as

not to put my body through quite as much trauma all at once AND in his goal/hope

of better perfecting the artificial discs to implant in me at that area at that

time.

Dr. Callewart was, as always, forthright, direct, and very frank with both me

and my immediate family (all of whom were present) about the surgical risks for

me, including but not limited to: stroke, paralysis, decreased neck mobility,

increased and/or the same level of very high chronic pain level, and death. He

specifically asked to be certain that I have a current Directive to Physicians

and a Living Will. I do. He said that he was reasonably certain that I will be

in a high level of chronic pain and require pain management and pain meds for

the rest of my life. He further explained in detail that he will go in through

the 1999 anterior incision site, how long he anticipates the surgery to last

(pending whether he sees with his eyes and feels with his hands more damage

like he did in 1999), that I will be hospitalized a MINIMUM of 2 days and

nights, that I will be very incapacitated for a MINIMUM of one month afterwards,

that during that time I will require A LOT of assistance with self-help

(bathing, using the toilet, having meals prepared and served to me (and possibly

even fed to me for awhile), that I will be unable to drive during recuperation

(and possibly permently due to decreased neck mobility), that he may recommend

home health care (and will assist me in dealing with my ins regarding that) and

even possibly me going to a skilled nursing facility during the first and most

difficult part pf my recuperation period (due to my multiple medical problems,

slow healing history, etc).

I told him that I trust him with my life and whole heart, that I KNOW he is

not just my doctor but my FRIEND, and that if success is possible, he will

succeed....and if he doesn't, it won't be his fault. He smiled and verbally

assured me that all of this is VERY TRUE. And so now, I await the c-spine

fusion on Sept. 9 (earlier if they happen to have a cancellation, which they

sometimes do). I must rest now. This email has taken a great deal out of me

physically. ALL GOOD THOUGHTS ANA PRAYERS ARE GREATLY WANTED APPRECIATED. I

love each and every one of my " family of choice "

Love,

~LoneStarRose~

(~~)

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,

My prayers are with you too. It sounds like your doctor is

excellent as you say and will take great care of you. I was told I

couldn't have any spinal fusion surgery because I had too many

levels involved. All but the first one at the top (C1-C2) are

bulging out and two are herniated, one of them burst and leaked out.

The fluid calcified and is now touching the spinal cord so that if I

lift much or am in the wrong position it causes considerable

problems. I am on chronic pain meds at what they consider a " very

high dose " . If you have any questions about that, I can help and/or

give you some good resources. Keep in touch, and of course vent if

you need to. You have been through this before and it's

understandable if you have apprehensions. Do you think you will do

well on home health care?

Prayers & (((hugs))),

~Duv ()

> I am using the laptop on a tray, but even that hurts so cannot be

on the computer long. My recent cervical myleogram, CT scan, and

EMG (nerve conduction test on my upper body) were all abnormal.

All indicated " remarkable " and " significant " abnormalities at c 3-4

and c-6-7 as well as he congenital narrowing of my spinal column

from c-3 to t-1 (that part can't be changed nor corrected). Disc

bulging and vertebrae degeneration at those locations posterially,

anterially, and bilaterally. Pinched nerves particularly

significant at c-6-7 causing pain, numbness, and tingling to

constantly run down my right arm and outer two digits on my right

hand. Pinched nerves and disc and vertebrae abnormalities also

causing significant pain on the right shoulder (as well as

significant muscle spasming and pain), base of my skull in back,

upper back on right side, and in front on and between both collar

bones. Not a pretty picture.

>

> My long term and VERY TRUSTED orthopedic surgeon, Dr. Craig

Callewart, has strongly recommended an extension of my 1999 cervical

fusion at c-6-7, which has beeb scheduled for Sept. 9, 2004 at

Baylor Dallas (EXCELLENT hospital). Dr. Callewart told me that he

and some of his colleagues are currently trying to perfect

some " higher tech " artificial discs, but " have only implanted approx

60 in patients so far " . Therefore, he wants to " improve them " and

does NOT want to implant any in me at this time due to all of my

other medical issues, particularly my Ehlers-Danlos Syndrome. He

stressed that IM will undoubtedly require another cervical fusion at

c-3-4, but as that area is not as urgently in need of surgical

intervention, he wants to try to wait another 9=12 months so as not

to put my body through quite as much trauma all at once AND in his

goal/hope of better perfecting the artificial discs to implant in me

at that area at that time.

>

> Dr. Callewart was, as always, forthright, direct, and very frank

with both me and my immediate family (all of whom were present)

about the surgical risks for me, including but not limited to:

stroke, paralysis, decreased neck mobility, increased and/or the

same level of very high chronic pain level, and death. He

specifically asked to be certain that I have a current Directive to

Physicians and a Living Will. I do. He said that he was reasonably

certain that I will be in a high level of chronic pain and require

pain management and pain meds for the rest of my life. He further

explained in detail that he will go in through the 1999 anterior

incision site, how long he anticipates the surgery to last (pending

whether he sees with his eyes and feels with his hands more damage

like he did in 1999), that I will be hospitalized a MINIMUM of 2

days and nights, that I will be very incapacitated for a MINIMUM of

one month afterwards, that during that time I will require A LOT of

assistance with self-help (bathing, using the toilet, having meals

prepared and served to me (and possibly even fed to me for awhile),

that I will be unable to drive during recuperation (and possibly

permently due to decreased neck mobility), that he may recommend

home health care (and will assist me in dealing with my ins

regarding that) and even possibly me going to a skilled nursing

facility during the first and most difficult part pf my recuperation

period (due to my multiple medical problems, slow healing history,

etc).

>

> I told him that I trust him with my life and whole heart, that I

KNOW he is not just my doctor but my FRIEND, and that if success is

possible, he will succeed....and if he doesn't, it won't be his

fault. He smiled and verbally assured me that all of this is VERY

TRUE. And so now, I await the c-spine fusion on Sept. 9 (earlier if

they happen to have a cancellation, which they sometimes do). I

must rest now. This email has taken a great deal out of me

physically. ALL GOOD THOUGHTS ANA PRAYERS ARE GREATLY WANTED

APPRECIATED. I love each and every one of my " family of choice "

> Love,

>

>

> ~LoneStarRose~

> (~~)

>

>

>

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Guest guest

My prayers are with you . I know about the pain your going threw. I got the

same results from an MRI but in my lower back. They also found a hole in my

spine where they think the nerve damage is being done. There are days where I

can't walk. So far they have me an Darvacet, what a joke that is. Because of my

EDS they are going to make me wait another 3 months and do another MRI to see if

anything has changed. SO in the meantime I suffer with chronic pain and not

being able to lift more then 5 lbs. Yeah Right! I wish I had a Doc like yours.

HUGGLES,

Grace

EMG&Myleogram reports:FUSION NOW SCHEDULED

I am using the laptop on a tray, but even that hurts so cannot be on the

computer long. My recent cervical myleogram, CT scan, and EMG (nerve

conduction test on my upper body) were all abnormal. All indicated " remarkable "

and " significant " abnormalities at c 3-4 and c-6-7 as well as he congenital

narrowing of my spinal column from c-3 to t-1 (that part can't be changed nor

corrected). Disc bulging and vertebrae degeneration at those locations

posterially, anterially, and bilaterally. Pinched nerves particularly

significant at c-6-7 causing pain, numbness, and tingling to constantly run down

my right arm and outer two digits on my right hand. Pinched nerves and disc and

vertebrae abnormalities also causing significant pain on the right shoulder (as

well as significant muscle spasming and pain), base of my skull in back, upper

back on right side, and in front on and between both collar bones. Not a pretty

picture.

My long term and VERY TRUSTED orthopedic surgeon, Dr. Craig Callewart, has

strongly recommended an extension of my 1999 cervical fusion at c-6-7, which has

beeb scheduled for Sept. 9, 2004 at Baylor Dallas (EXCELLENT hospital). Dr.

Callewart told me that he and some of his colleagues are currently trying to

perfect some " higher tech " artificial discs, but " have only implanted approx 60

in patients so far " . Therefore, he wants to " improve them " and does NOT want to

implant any in me at this time due to all of my other medical issues,

particularly my Ehlers-Danlos Syndrome. He stressed that IM will undoubtedly

require another cervical fusion at c-3-4, but as that area is not as urgently in

need of surgical intervention, he wants to try to wait another 9=12 months so as

not to put my body through quite as much trauma all at once AND in his goal/hope

of better perfecting the artificial discs to implant in me at that area at that

time.

Dr. Callewart was, as always, forthright, direct, and very frank with both me

and my immediate family (all of whom were present) about the surgical risks for

me, including but not limited to: stroke, paralysis, decreased neck mobility,

increased and/or the same level of very high chronic pain level, and death. He

specifically asked to be certain that I have a current Directive to Physicians

and a Living Will. I do. He said that he was reasonably certain that I will be

in a high level of chronic pain and require pain management and pain meds for

the rest of my life. He further explained in detail that he will go in through

the 1999 anterior incision site, how long he anticipates the surgery to last

(pending whether he sees with his eyes and feels with his hands more damage

like he did in 1999), that I will be hospitalized a MINIMUM of 2 days and

nights, that I will be very incapacitated for a MINIMUM of one month afterwards,

that during that time I will require A LOT of assistance with self-help

(bathing, using the toilet, having meals prepared and served to me (and possibly

even fed to me for awhile), that I will be unable to drive during recuperation

(and possibly permently due to decreased neck mobility), that he may recommend

home health care (and will assist me in dealing with my ins regarding that) and

even possibly me going to a skilled nursing facility during the first and most

difficult part pf my recuperation period (due to my multiple medical problems,

slow healing history, etc).

I told him that I trust him with my life and whole heart, that I KNOW he is

not just my doctor but my FRIEND, and that if success is possible, he will

succeed....and if he doesn't, it won't be his fault. He smiled and verbally

assured me that all of this is VERY TRUE. And so now, I await the c-spine

fusion on Sept. 9 (earlier if they happen to have a cancellation, which they

sometimes do). I must rest now. This email has taken a great deal out of me

physically. ALL GOOD THOUGHTS ANA PRAYERS ARE GREATLY WANTED APPRECIATED. I

love each and every one of my " family of choice "

Love,

~LoneStarRose~

(~~)

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