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Just signed up here tonite. I was diagnosed with MS one year ago.

I am 53--almost 54. Blessed to be very mild, but last year was

quite rough--numb from the neck down and lots of pain. I have

probably had this for about 20 years. My first numbness was my

entire left side in the mid 80's. All kinds of tests, but nothing

found. I think I am glad since the treatments are greatly improved

now. I take Avonex, most generally do my own injections. Sometimes

have almost no reaction, just a little achy and headachy.

Sometimes, feel pretty rough for 24 hours.

I am very lucky to have a supportive family and very supportive

husband. We have been married for 33 years, and this has been a huge

adjustment. I do work, but cut back to 32 hours per week due to

exhaustion.

I just had my first year MRI to see what is going on and how the

meds are handling this disease. Get my results on Friday. Have a

great doctor who is very patient in answering all my questions and

returning calls very promptly. I also have been very lucky in that

this has never yet affected my vision. I did have to do 5 days of

intense IV therapy last year to break the numbness cycle. My

biggest problem is exhaustion and pain in my hands and feet. The

vibrations in my legs have become pretty rare, but when I am tired

and stressed my right foot and hand tingle and go numb.

As I said above, I am married, we have two grown married daughters.

I have my first grandchild born in June....he is a real ray of

sunshine. My other daughter and her husband are in the process of

adopting from China--after 9 years of trying they have given up on

the fertility treatments. Can't say I blame them. Sooooo..this

time next year, I should have a granddaughter also. That will

great.

Look forward to getting to know all of you

Dan, hope your foot feels better.

Shari

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Dear Shari:

Welcome to the group, sounds like you are handling life on its terms, healthy attitude. I'm glad to have you as a member.

How exciting to be a grandma..I can't wait. I have friends who adopted from China, I think it is great, such beautiful people. I'm going to have to light a fire under my son and daughter in law, LOL.

Bette

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Welcome Shari. It is nice to meet you.

Margot

>

> Just signed up here tonite. I was diagnosed with MS one year ago.

> I am 53--almost 54. Blessed to be very mild, but last year was

> quite rough--numb from the neck down and lots of pain. I have

> probably had this for about 20 years. My first numbness was my

> entire left side in the mid 80's. All kinds of tests, but nothing

> found. I think I am glad since the treatments are greatly improved

> now. I take Avonex, most generally do my own injections. Sometimes

> have almost no reaction, just a little achy and headachy.

> Sometimes, feel pretty rough for 24 hours.

>

> I am very lucky to have a supportive family and very supportive

> husband. We have been married for 33 years, and this has been a huge

> adjustment. I do work, but cut back to 32 hours per week due to

> exhaustion.

>

> I just had my first year MRI to see what is going on and how the

> meds are handling this disease. Get my results on Friday. Have a

> great doctor who is very patient in answering all my questions and

> returning calls very promptly. I also have been very lucky in that

> this has never yet affected my vision. I did have to do 5 days of

> intense IV therapy last year to break the numbness cycle. My

> biggest problem is exhaustion and pain in my hands and feet. The

> vibrations in my legs have become pretty rare, but when I am tired

> and stressed my right foot and hand tingle and go numb.

>

> As I said above, I am married, we have two grown married daughters.

> I have my first grandchild born in June....he is a real ray of

> sunshine. My other daughter and her husband are in the process of

> adopting from China--after 9 years of trying they have given up on

> the fertility treatments. Can't say I blame them. Sooooo..this

> time next year, I should have a granddaughter also. That will

> great.

>

> Look forward to getting to know all of you

>

> Dan, hope your foot feels better.

>

> Shari

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  • 5 years later...

I take 4.5 mp low dose naltrexone for my fibromyalgia and the effects have been

amazing! No side effects and inexpensive, so it doesn't hurt to try it, unlike

other big pharma meds. A google search will turn up lots of info. Good luck!

> >

> > My name is Margie, I thought I posted this morning about a drug call

naproxen, I wanted to know if anyone has been on this and if they have any

information about it. Thank you

> >

>

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