ldn feeding tube

[Guest guest]

thanks for all those great replys about cancerand ldn for my friend, now i need

to as is anyone here on feeding tube and taking ldn thru the tube?

i am ready now to restart brother with his ldn but will start at half of the 4.0

dose

nowthat his body is off and clear of antibiotics we are going to start fresh

with his ldn and vitamins and supplements.

now his only actual drug hes taking is keppra 1 tsp 2x daily and as needed

adavan everything else is over the counter.

so could some of you MSers please tell me what you are taking and how much as to

your vitamins and minerals?

everything we give brother is thru his tube so we are also planning on making a

drastic change to food blended as i think his can nutrition is causing most of

his sticky mucus.mark has had ms for 16 yrs now but been under my care for past

7 yrs

hate it when we need to start over but sometimes it can be a blessing because i

get to reevaluate all thats going into him and why

so jump on board please tell me what your thoughts are for restarting mark

back on his supplements.LOL well i know he will get started just not sure on

what yet thats what i guess i mean thanks group you have been lifesaver to

many and for mark many times:)

nancy sister and caregiver to brother with ms

[Guest guest]

Art

My MS/LDN story/1988 - 2010

http://ldn.proboards.com/index.cgi?board=personal & action=display & thread=867

>

> thanks for all those great replys about cancerand ldn for my friend, now i

need to as is anyone here on feeding tube and taking ldn thru the tube?

> i am ready now to restart brother with his ldn but will start at half of the

4.0 dose

> nowthat his body is off and clear of antibiotics we are going to start fresh

with his ldn and vitamins and supplements.

> now his only actual drug hes taking is keppra 1 tsp 2x daily and as needed

adavan everything else is over the counter.

> so could some of you MSers please tell me what you are taking and how much as

to your vitamins and minerals?

> everything we give brother is thru his tube so we are also planning on making

a drastic change to food blended as i think his can nutrition is causing most of

his sticky mucus.mark has had ms for 16 yrs now but been under my care for past

7 yrs

> hate it when we need to start over but sometimes it can be a blessing because

i get to reevaluate all thats going into him and why

> so jump on board please tell me what your thoughts are for restarting mark

back on his supplements.LOL well i know he will get started just not sure on

what yet thats what i guess i mean thanks group you have been lifesaver to

many and for mark many times:)

> nancy sister and caregiver to brother with ms

>

[Guest guest]

I would consider using theLDN transdermal cream as it is important that LDN be released fast and it would be easier to use, too. Any pharmacist can contact Dr. McCandless' pharmacist who created the transdermal cream for her to prescribed to her patients.

mjh

[Guest guest]

Hi ,

I run a group for people with ALS, many of whom have problems with

sticky mucus. Most find eliminating dairy can help significantly plus

quite a few have found NAC (n-acetyl-cysteine) helps minimise and/or

eliminate it together with LDN.

Cheers,

PS You are obviously a very caring sister!!

nancy m wrote:

thanks for all those great replys about cancerand ldn for my friend, now i need to as is anyone here on feeding tube and taking ldn thru the tube?

i am ready now to restart brother with his ldn but will start at half of the 4.0 dose

nowthat his body is off and clear of antibiotics we are going to start fresh with his ldn and vitamins and supplements.

now his only actual drug hes taking is keppra 1 tsp 2x daily and as needed adavan everything else is over the counter.

so could some of you MSers please tell me what you are taking and how much as to your vitamins and minerals?

everything we give brother is thru his tube so we are also planning on making a drastic change to food blended as i think his can nutrition is causing most of his sticky mucus.mark has had ms for 16 yrs now but been under my care for past 7 yrs hate it when we need to start over but sometimes it can be a blessing because i get to reevaluate all thats going into him and why

so jump on board please tell me what your thoughts are for restarting mark back on his supplements.LOL well i know he will get started just not sure on what yet thats what i guess i mean thanks group you have been lifesaver to many and for mark many times:)

nancy sister and caregiver to brother with ms