THIS PAST SUMMER I WAS DOING WODERFUL. WAS OUT N ABOUT, HUNG AT THE POOL DAM NEAR EVERYDAY. DID NOT HAVE ANY PAIN. THEN SEPT ROLLS AROUND N SO DOES THE PAIN, AT FIRST I CONTACT MY NERO N YES I GET UR MS IS ACTING UP N U NEED THE ROIDS. SO 2 DAYS WORTH N THREE WEEKES LATER STILL FEELING THE PAIN N NOW GOT NUMBNESS SO BAD IN MY FINGERS THAT I HAD TROUBLE USING MY HANDS. SLEEPING WAS SO BAD COULD HARDLY LAY IN BED. FUNNY THING HAPPEN THE OTHER NITE. I GOT A VISION N FOLLOWED UP ON IT THE NEXT DAY. ALL THESE YEARS I HAVE 4GOTTEN THAT I ALSO HAVE FIBO AS AN UNDERLINE 2 MY MS. SO I KNEW I HAD A DOCTORS APPT YESTERDAY 2 GET MY FLU SHOT N THOUGHT 2 MYSELF...THIS COULD IN FACT B MY FIBRO N NOT MY MS. WHEN MY MS ACTS UP I GET THAT FOGGY FEELING N HAVE NOT HAD THAT IN OVER A YEAR. SO INTO THE DOC'S OFFICE I GO, I TELL HER WHAT I HAVE BEEN FEELING N ASK IF THIS COULD B MY FIBRO. SHE ASKED DID I TALK 2 MY NERO N I TOLD HER EVERYTIME I DO I GET ITS UR MS LETS GET U ON THE ROIDS. SO SHE DID THE FIBRO TEST U KNOW WHERE THEY PRESS ON UR POINTS 2 C HOW MANY U HAVE N I GOT 18 OUT OF 18.....BINGO. AFTER GETTING MY SHOT SHE GAVE ME A SCRIPT 4 FLEXERIL, I TOOK 5MGS LAST NITE N WOKE UP THIS MORNING IN NO PAIN, NO SWELLING N NO NUMBNESS. I FEEL A BIT HUNG OVER THO BUT AM NOT SURE IF ITS MY BODY NEEDING 2 GET USED 2 NEW MED OR A COMBO OF NEW N OLD MEDS N FLU SHOT. WILL C HOW I FEEL 2MORROW MORNING.
SO MY WORD OF ADVICE 2 THOSE THAT HAVE UNDERLINE CONDITIONS 2 THERE MS AS I DO, CHECK ALL DENAMINATORS B4 SAYING ITS MY MS. AS I PUT IN MY TITLE THEY DON'T KNOW IT ALL.....
OK GUYS N GALS GRAB A SEAT MAKE SURE U HAVE UR SODA'S, POPCORN N GUGEEFRIUTS THIS MAY BE A LONG ONE...
OK SO I HAD MY MRI DONE ON JUNE 30TH, 2008
HERE R MY RESULTS......
16 LESIONS IN ALL SO NO CHANGE THERE WITHIN THE PAST 3 YEARS N ALL 16 R NON-ACTIVE WOOHOOO GREAT NEWS. HOWEVER HE THINKS THEIR MAY BE ONE ACTIVE LESION IN MY SPINE BUT NOT SURE. DOESN'T THINK I NEED 2 HAVE AN MRI OF MY SPINE DONE AS YET. WILL WAIT UNTIL NEXT CHECK UP ON SEPT. 24TH, 2008 N C IF THERE R ANY CHANGES.
HAD MY VISIT WITH MY GENERAL DOCTOR ON JULY 17TH, 2008
N HERE IS HOW THAT WENT....
TOLD HER ABOUT THE HEARING LOSS IN MY RIGHT HEAR, SO SHE CHECK FROM MY CHEST 2 MY THROAT 2 MY NOSE N THEN MY EARS COME UP WITH NOTHING. SHE FELT THAT THE HEARING LOSS MAY BE FROM THE MS. SHE THEN CHECK MY SPINE N SAID IT WAS VERY INFLAMED HAD ALOT OF INFLAMATION N FELT I SHOULD BE PUT ON ORAL STERIODS AT THAT POINT. I TOLD HER I HAVE MY NEURO APPT THE FOLLOWING WEEK, SO SHE DECIDE 2 WRITE A REPORT 2 MY NEURO DOCTOR N LET HIM DECIDE THEN. I DON'T LIKE TAKING THE ORAL STERIODS, GET VERY BAD SIDE AFFECTS FROM THEM. I DID ASK HER ABOUT GETTING SOMETHING 4 THE PAIN IN MY SPINE BECUASE IT WAS SO BAD. SHE GAVE ME LIDOCANE PATCHES.
OK NOW ONTO MY NEURO APPT. ON JULY 24TH, 2008
N HERE IS HOW IT WENT......
HE CHECKED ME OUT N I TOLD HIM ABOUT THE HEARING LOSS N WE SPOKE ABOUT WHAT MY GENERAL DOCTOR HAD 2 SAY. HE SAID FIRST HE WANTED ME 2 HAVE A HEARING TEST DONE SO WE CAN SEE WHATS GOING ON THERE. HE ALSO TOLD ME THAT HE FELT THAT LDN WAS NOT WORKING 4 ME, I ASKED HIM HOW IS HE COMING 2 THIS DECISION, HIS ANSWER WAS THAT I HAD 2 FLAIR UPS SINCE BEING ON IT (NOT EXSACERBATIONS). I TOLD HIM IF THATS HOW U R MAKING THAT DECISON THEN LETS GO BACK FURTHER WHEN I WAS ON COPAOXNE N AVONEX I HAD FLAIR UPS ON THOSE AS WELL N WHEN I HAD 2 HAVE THE STERIOD INFUSIONS THEN IT WAS A TOTAL OF 5 DAY TREATMENT N THEN ORAL. THESE PAST 2 FLAIR UPS WERE TREATED WITH JUST 3 DAY TREATMENTS N NO ORAL. HE THEN TOLD ME THAT HE DOES NOT REALLY KNOW THE MACANICS ON HOW LDN WORKS 4 SOME N NOT OTHERS N THAT MOST OF HIS PATIENTS HAVE ASKED 2 BE TAKEN OFF. WE THEN TALK ABOUT MY BIGEST PROBLEM WITH MY MS N THAT WOULD BE THE INFLAMTION I GET IN MY SPINE MY RIG CAGE (MS HUG) N MY FINGERS ON MY LEFT HAND. SO TALKED SOME MORE N DECIDED 2 KEEP ME ON THE LDN N ADD A ONCE A MONTH IV STERIOD INFUION IN HOPES OF THAT KEEPING MY INFLAMTION AT BAY, TIME WILL TELL. I ALSO TOLD HIM THAT I FELT THAT THE BACOLFEN WOULD WORK ON SOME NITES BUT NOT ON OTHERS. I THINK WHEN I GET THE MS HUG REALLY BAD IT DOES NOT WORK AT NITE SO HAVE TROUBLE SLEEPING. SO WE HAVE ADDED ZANAFLEX 2MG AT NITE WHEN NEEDED N STILL CAN TAKE THE BACLOFEN DURING THE DAY WHEN NEEDED.
OK NOW ON 2 MY ENT APPT. ON JULY 29TH, 2008
HERE IS HOW THAT WENT....
THE DOCTOR ALREADY KNOWS ABOUT MY MS, GO THERE 4 MY ALLERGIES. HE SAID HE WAS AMASED THAT I HAVE NOT BEEN THERE IN SOME TIME N HAD ASKED HOW MY ALLERGIES HAVE BEEN. I TOLD HIM ABOUT BEING ON LDN N THINK THAT IT IS ALSO HELPING WITH MY ALLEGIES N HAVE HEARD IT HAS HELP OTHERS WITH THEIRS AS WELL. HE TOLD ME HE WAS GOING 2 DO SOME RESEARCH ON LDN. HE THEN CHECKED OUT MY EARS DID NOTICE SOME WAX DEEP IN THE EAR SO HAD THEM CLEANED OUT. THEN ONTO THE HEARING TEST. AFTER THAT WAS DONE BOTH DOCTORS CAME INTO THE ROOM N MY FIRST IMPRESSION WAS O NO. BUT IT WAS THE TOTAL OPOSITE. THEY TOLD ME ALOT OF PPL WHO WITH MS NOT ONLY HAVE TROBLE WITH THEIR EYES ON SOME LEVEL BUT ALSO HAVE TROUBLE WITH THEIR HEARING ON SOME LEVEL AS WELL. THEY COULD NOT BELIEVE HOW GOOD MY HEARING WAS I COULD HEAR A PIN DROP. WE THEN TALKED SOME MORE ABOUT THE SYMPTOMS I AM HAVING N THEY THINK BUT CAN'T BE SURE UNTIL THEY SEE IT WITH THEIR OWN EYES THAT IT CAN BE FROM THE INFLMATION. HE WANTS ME 2 CALL THEM THE NEXT TIME I GET THIS HEARING LOSS N WILL REDO THE TESTING THAT DAY.
HAD MY FIRST MONTHLY IV STERIOD INFUION DONE YESTERDAY JULY 30TH, 2008. WENT WELL NO SIDE EFFECTS FIRST NITE. TOOK SOME BENADRYL 2 GET A GOOD NITE SLEEP N IT WORKED.
SO AS OF 2DAY I AM STILL GOING 2 TAKE MY LDN. LDN IS NOT HELPING WITH ALL OF MY SYMPTOMS,BUT HERE IS WHERE IT HAS HELPED ME. IT HAS CLEARED UP THE FUZZY IN MY HEAD. HAS CLEARED UP MY BLADDER ISSUES AT NITE. N EVEN THO I STILL HAVE 2 USE MY SCOOTER OR MOTORIZE CHAIR 4 DISTANCE I DO WALK THE SHORT DISTANCE BETTER THEN I HAD A YEAR AGO. THERE IS A NEW MED THAT IS GOING 2 BE RELEASED IN 09 OR 10, THEY R TRYING 2 PUSH 4 09. ITS CALLED FAMPRIDINE THIS DRUG IS IN TRAIL N HAS SHOWN GREAT PROMISE IN HELPING WITH SPAUMS N NERVE PAIN N WILL HELP WITH THE INFLAMATIONS THAT THE SPAUMS N NERVE PAIN CAN CAUSE. MY DOCTOR HAS PUT ME ON THE LIST 2 BE 1 OF THE FIRST 2 START TAKING THIS WHEN IT COMES OUT. SO I WILL BE ADDING THIS ALONG SIDE MY LDN THINK THEY WILL MAKE A GOOD COMBO 4 ME.
I AM A REALALIST WHEN IT COMES 2 MY MS. I KNOW THEIR IS NO CURE OR WILL BE ONE 4 QUITE SOME TIME. BIT I AM DESTINE 2 LIVE A NORMAL LIFE AS BEST I CAN SO WILL RESEARCH ALL DRUGS OUT THERE N AM WILLING 2 GO THROUGHT TRIAL N ERROR UNTIL I GET THE RIGHT COMBO OF DRUGS THAT WILL ALLOW ME 2 LIVE THAT NORMAL LIFE.
I HAVE STATED PT AT HOME 3 DAYS A WEEK, I HAVE A HOME HEALTH AID THAT COMES 2 DAYS A WEEK 2 HELP ME AROUND THE HOUSE. I HAVE MY INFUION NURSE THAT WILL BE HERE ONCE A MONTH N NOW MY PRIVATE NURSE THAT WILL BE DOING THE FOLLOW UP AFTER MY INFUIONS. SO U SEE I HAVE A GREAT TEAM THAT IS WORKING WITH ME 2 MAKE SURE I LIVE AS NORMAL A LIFE AS I POSSIBLE CAN....
Comments
Comments
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WATCH OUT FOR THAT BEE!
the graphics are cute but I think it makes your voice and video out of sync
So when ya gonna invite me to the pool? huh huh? LOL
As for your MRI, this would be the Baseline to compare all future ones to.
I'm gone... won't be back til 7/22... wrote about it in my journals. Have fun :)






I read this on the LDN page. I'm happy about your hearing.
DellaJeanne
Wow -you've been busy with the docs! Glad your hearing is better though!! Keep us updated!!
GoAwayMS
I can see what you mean about a round of Drs, hope that the answers help you. You are sure keeping positive which is great. Keep up the research too.
Hugs
AusSue
unfortunately i can't say that ldn had completely helped me...my neuro said if he saw anything wrong he was pulling me off of it...when he found the lesions in brain inactive but the one in spine active he stuck me in hospital for iv steroids and then orals for 30 days....now i am at a loss because i am not on any meds right now..fighting insurance (medicaid) and losing of course....now up the creek...will try the glyconutrient which my dad is pushing me to do and will wait to see if my new insurance will pick up the copaxone...i wish you luck with the ldn...i know it helps some but in my case not sure what it did for the better...can't put my finger on it and really just trying to slow down the disease so i can live...be blessed NTK and thanks for the journal entry...what did your doctor say when the disease goes into remission on it's own?
CASMIRA