Re: Post MRI changes for MS/LDN

[Guest guest]

Hi Everyone,

If anyone with MS can post their experiences regarding their MRI's before and after LDN I would greatly appriciate the info. We are trying to see if doing a study or questianair in this area would be benificial.

Thanks, Aletha

[Guest guest]

Re: Day 1500 - 05/25/07

I had a baseline closed Tesla 1.5 brain MRI 8/04.I just had a follow up Brain MRI done 4/19/07, with comparison. The report was: No Progression shown, virtually identical to the previous one. I had a Cervical and Thoracic MRI 4/20/07, but the C & T previous set was from 8/02, and this Thoracic showed my T5 "area of sclerosis" was healed, no abnormalities on my Thoracic at all.My Cervical showed my C5 "two lesions" from 7/02 were healed, and showed MS in my C2/C3 that wasn't there in 8/02, 8 months before starting LDN. My chiros said I had C2/C3 issues since before starting LDN.

Re: [low dose naltrexone] Re: Post MRI changes for MS/LDN

Hi Everyone,

If anyone with MS can post their experiences regarding their MRI's before and after LDN I would greatly appriciate the info. We are trying to see if doing a study or questianair in this area would be benificial.

Thanks, Aletha

[Guest guest]

Thanks Larry,

Is there anyone else as well as Larry and DJ that can share their MRI experience with us?

Thanks

Aletha

Re: [low dose naltrexone] Re: Post MRI changes for MS/LDN

Hi Everyone,

If anyone with MS can post their experiences regarding their MRI's before and after LDN I would greatly appriciate the info. We are trying to see if doing a study or questianair in this area would be benificial.

Thanks, Aletha

[Guest guest]

I have been on LDN for 2 years September 3rd and in January I was living in Maine and my Neurologist there did a full MRI and it showed that I had 10 lesions on my brain. I ended up moving to Georgia and around April my new Neurologist did a new MRI just on my brain and all lesions were gone.

My new Neurologist looks at the MRI first before he looks at who's it is to see what he can see and when he looked at mine and saw nothing then looked at my chart to see who I was and what I had, he said by not seeing your chart I would of told you that you had nothing wrong.

Hugs & Blessings,

Crystal

LDN_Users Group Owner

Diagnosed November 2004 with Secondary Progressive MS, Transverse Myelitis and an Advocate for LDN!! 2 years on LDN with Skip's Pharmacy.....

Crystal's MS,TM & LDN Website

Crystal's LDN Gift Shop

Crystal's LDN Support Group

Skip's Compounding Pharmacy

MS & TM Spouse & Caregiver Support Group

Re: [low dose naltrexone] Re: Post MRI changes for MS/LDN

Hi Everyone,

If anyone with MS can post their experiences regarding their MRI's before and after LDN I would greatly appriciate the info. We are trying to see if doing a study or questianair in this area would be benificial.

Thanks, Aletha__________________________________________________

[Guest guest]

Everyone who was at the LDN conference, in the testimonials that were

not folded but yet stapled together in the upper lefthand corner...the

back two pages are from a former patient of Dr. Bihari's, her latest

MRI results are there. She was once a member of this forum but the

numerous off-topic posts we were having at one time caused her

departure from the forum.

[Guest guest]

Maybe that's one reason why we're having so many people wanting to

unsubscribe lately? Too many off-topic posts unrelated to LDN?

Art

--

>

>

> Everyone who was at the LDN conference, in the testimonials that were

> not folded but yet stapled together in the upper lefthand

corner...the

> back two pages are from a former patient of Dr. Bihari's, her latest

> MRI results are there. She was once a member of this forum but the

> numerous off-topic posts we were having at one time caused her

> departure from the forum.

>

>

>

[Guest guest]

Crystal:

With all of the lesions gone, did your symptoms also disappear? That is a question that I have not been able to find an answer to.

Thanks

LDN

MS

Re: [low dose naltrexone] Re: Post MRI changes for MS/LDN

Hi Everyone,

If anyone with MS can post their experiences regarding their MRI's before and after LDN I would greatly appriciate the info. We are trying to see if doing a study or questianair in this area would be benificial.

Thanks, Aletha____________ _________ _________ _________ _________ __

[Guest guest]

I would also like to know if they were open MRI's oe closed MRI's? Hawthorne <wendy.hawthorne@...> wrote: Crystal: With all of the lesions gone, did your symptoms also disappear? That

is a question that I have not been able to find an answer to. Thanks LDN MS Re: [low dose naltrexone] Re: Post MRI changes for MS/LDN Hi Everyone, If anyone with MS can post their experiences regarding their MRI's before and after LDN I would greatly appriciate the info. We are trying to see if doing a study or questianair

in this area would be benificial. Thanks, Aletha____________ _________ _________ _________ _________ __

[Guest guest]

Yes Id be very interested to see those too althea, before I start

the LDN it would be nice to see if its halting progression.

Helen ))))

-- In low dose naltrexone , " Aletha Wittmann "

<Aletha@...> wrote:

>

> Hi Everyone,

>

> If anyone with MS can post their experiences regarding their MRI's

before and after LDN I would greatly appriciate the info. We are

trying to see if doing a study or questianair in this area would be

benificial.

>

> Thanks, Aletha

>

[Guest guest]

Hi Helen

If progression shows up by way of lesions on MRI`s then to my

knowledge, my husband`s MS has not progressed since starting LDN

nearly three years ago. I dont have the the reports of the three

MRI`s he`s had to hand but I remember quite clearly that last year`s

MRI showed no new lesions (and he has a lot!) and some

had " disappeared " . We are going to get the results of the latest one

in about 6 weeks time. has had no new symptoms or

disabilites occur and no exaserbations. He does have some disability

in the form of some balance problems, cognitive issues and bad

fatigue but he had all these things before he started LDN. They

havent gone away or gotten any worse. He has never had any numbness

or pain and only one bad episode of eye problems in the very

beginning.

We like to think the LDN has protected him from any progression

occuring. As soon as we get the latest MRI results I`ll post them

here.

-- In low dose naltrexone , " helen.padgett "

<helen.padgett@...> wrote:

>

> Yes Id be very interested to see those too althea, before I start

> the LDN it would be nice to see if its halting progression.

> Helen ))))

>

>

>

>

>

>

>

>

> -- In low dose naltrexone , " Aletha Wittmann "

> <Aletha@> wrote:

> >

> > Hi Everyone,

> >

> > If anyone with MS can post their experiences regarding their

MRI's

> before and after LDN I would greatly appriciate the info. We are

> trying to see if doing a study or questianair in this area would be

> benificial.

> >

> > Thanks, Aletha

> >

>