Laura's Personal PN Story Line

(Note: Information on the pages of this web site should not be considered medical opinion(s)
Always consult your doctor before trying any treatment or medication.)...

MY NAME IS LAURA. I'M A 30 YR. OLD MOTHER OF THREE AND

I HAVE PN aka PARSONAGE TURNER SYNDROME aka BRACHIAL PLEXOPATHY.

WELL WHATEVER IT IS,

IT STINKS !!!

O.K. GOT THAT OUT...

I HAD SURGERY ON TWO HERNIATED DISC IN MY CERVICAL SPINE.

THE PROCEDURE WAS CALLED ANTERIOR CERVICAL DISCECTOMY AND FUSION. I GUESS THEY WERE COLLAPSED PRETTY BAD AND ON SOME NERVES. CAUSE OF THE HERNIATION IS NOT KNOWN (NO ACCIDENT OR FALL ETC...).

THE SYMPTOMS OF PAIN AND MUSCLE SPASMS IN MY RIGHT ARM STARTED IN FEBRUARY, 1999. FINALLY I GOT AN MRI IN LATE MARCH, 1999, WHICH REVEALED THE HERNIATION. FROM THAT POINT I WAS REFERRED TO A NEUROSURGEON WHO DID THE OPERATION IN LATE
SEPTEMBER, 1999.

WELL IT IS NOW FEBRUARY, 2000, AND I'M STILL SUFFERING FROM A LOT OF PAIN, MUSCLE SPASMS, SEVERE WEAKNESS, LOSS OF GRIP -- THE LIST GOES ON...

I AM TAKING MEDICATIONS TO HELP WITH PAIN. I WILL BE STARTING PHYSICAL THERAPY
NEXT WEEK.

I AM OPTIMISTIC OF MY RECOVERY ALTHOUGH THE DOC SAYS THE DAMAGE

TO THE NERVES FROM THE HERNIATION PROVE THIS TO BE A PERMANENT IMPAIRMENT.

WE WILL JUST HAVE TO SEE WHERE THE LORD LEADS ME ON THIS.

I HAVE HAD TO STOP WORKING BECAUSE THE SYMPTOMS HAVE GOTTEN WORSE THAN
I EXPECTED;

BUT MY FAMILY IS THE BEST AND VERY SUPPORTIVE OF ME.

I DON'T KNOW IF I SHOULD APPLY FOR SSD OR SEE IF I GET BETTER.

TOO SOON TO TELL.

FOR NOW I WILL JUST REST KNOWING THRU GOD ALL THINGS ARE POSSIBLE AND

WITHOUT HIM IT WOULD BE MUCH WORSE!!!!!

I HOPE MY STORY HAS SHED A LITTLE LIGHT FOR SOME OR

MAYBE YOU CAN SHED SOME MY WAY.

IF SO E-MAIL ME ....

THANKS

LAURA

GRANL5@aol.com

P. S. I WILL UPDATE YOU ALL SOON.

GOD BLESS


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