Re: MS and muscle Spams...they stopped!

[Guest guest]

My mother has MS. I have been using MNRI with her as I can. I recently took the Tactile class in which Pamela said that Tactile helps with myelination. She mentioned a case which a child attending the camps wasn't myelinating and would die...apparently the child is still alive and myelinating...ask Pamela for the full story or take the Tactile class : )As a personal experience...my mother has muscle spasms which she takes medication to control. I do Tactile and some foot reflexes on her twice a week. One day I called her and said come over now...while the kids are happy...she popped over (1 block away) and I started the Tactile. She had not taken

her medication for the spasms yet...her leg and foot would spasm...so I'd just wait until it stopped then resume. We came down to working on the back of the body...doing the stretching on the legs. Her spasms stopped....and did not resume for the rest of the time I worked on her. It was strange...I guess because it was causing me stress as well but I could tell when the spams weren't coming back because the whole room felt so relaxed...I didn't say anything at first. After several minutes I mentioned they had stopped. So now I do that portion extra. I wish I could do an experiment and do the stretching throughout the day and see the difference between no meds/no stretching and no meds/stretching. Not sure I am able to do that though since both of us are really busy.Anyway, if you try it let us know how it works for you!!Hello,Does anyone have experience using MNRI successfully with Migraines and associated deep, white matter demyelination? Or possibly experience using MNRI with diseases of demyelination in general, like Multiple Sclerosis? Thanks.Messages in this topic (1)------------------------------------------------------------------------

[Guest guest]

Thank you for the input.

From: "Kayte" <k_sisler@...> Sent: Friday, July 15, 2011 10:03:45 AMSubject: RE: MS and muscle Spams...they stopped!

My mother has MS. I have been using MNRI with her as I can. I recently took the Tactile class in which Pamela said that Tactile helps with myelination. She mentioned a case which a child attending the camps wasn't myelinating and would die...apparently the child is still alive and myelinating...ask Pamela for the full story or take the Tactile class : )

As a personal experience...my mother has muscle spasms which she takes medication to control. I do Tactile and some foot reflexes on her twice a week. One day I called her and said come over now...while the kids are happy...she popped over (1 block away) and I started the Tactile. She had not taken her medication for the spasms yet...her leg and foot would spasm...so I'd just wait until it stopped then resume. We came down to working on the back of the body...doing the stretching on the legs. Her spasms stopped....and did not resume for the rest of the time I worked on her. It was strange...I guess because it was causing me stress as well but I could tell when the spams weren't coming back because the whole room felt so relaxed...I didn't say anything at first. After several minutes I mentioned they had stopped. So now I do that portion extra. I wish I could do an experiment and do the stretching throughout the day and see the difference between no meds/no stretching and no meds/stretching. Not sure I am able to do that though since both of us are really busy.

Anyway, if you try it let us know how it works for you!!

Hello,Does anyone have experience using MNRI successfully with Migraines and associated deep, white matter demyelination? Or possibly experience using MNRI with diseases of demyelination in general, like Multiple Sclerosis? Thanks.Messages in this topic (1)------------------------------------------------------------------------

[Guest guest]

That's fabulous. I have dystonia. It is somewhat related to MS. Even though I

was released from care by my neurologist 1.5 years ago it still has not totally

disappeared. I found that magnesium, B vitamins, and melatonin were more

effective than medications. Ironically the medications can cause symptoms; they

use the Parkinson class medications to treat dystonia. Activity can also affect

symptoms. There are several kinds of dystonia. Only 500,000 of us are identified

nationally and we are looking for the other 500,000. The c4d Care for Dystonia

was started by Beka Serdans, RN. She self-diagnosed. Brilliant lady and thank

you for this encouraging post. Alice McKeon

>

> My mother has MS.  I have been using MNRI with her as I can.  I recently took

the Tactile class in which Pamela said that Tactile helps with myelination.  She

mentioned a case which a child attending the camps wasn't myelinating and would

die...apparently the child is still alive and myelinating...ask Pamela for the

full story or take the Tactile class : )

> As a personal experience...my mother has muscle spasms which she takes

medication to control.  I do Tactile and some foot reflexes on her twice a week.

 One day I called her and said come over now...while the kids are happy...she

popped over (1 block away) and I started the Tactile.  She had not taken her

medication for the spasms yet...her leg and foot would spasm...so I'd just wait

until it stopped then resume.  We came down to working on the back of the

body...doing the stretching on the legs.  Her spasms stopped....and did not

resume for the rest of the time I worked on her.  It was strange...I guess

because it was causing me stress as well but I could tell when the spams weren't

coming back because the whole room felt so relaxed...I didn't say anything at

first.  After several minutes I mentioned they had stopped.  So now I do that

portion extra.  I wish I could do an experiment and do the stretching throughout

the day and see the

> difference between no meds/no stretching and no meds/stretching.  Not sure I

am able to do that though since both of us are really busy.

> Anyway, if you try it let us know how it works for you!!

>

> Hello,

>

> Does anyone have experience using MNRI successfully with Migraines and

associated deep, white matter demyelination? Or possibly experience using MNRI

with diseases of demyelination in general, like Multiple Sclerosis? Thanks.

>

>

>

>

>

>

>

>

> Messages in this topic (1)

>

>

>

>

>

> ------------------------------------------------------------------------

>