Re: Transfer Factor Formula 560

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<<< Does anyone have a sample of the Formula 560 I could buy from you

before I order an entire bottle? >>>

hi phil - i would, but i'm sorry, it doesn't work that way. you need to

take 3 a day for at least 2-3 mos. before you give it up. (and i can

tell you, after that, you won't want to give it up).

my oldest " charge " , " s " , had been a little haphazard about taking it -

she'd miss a day here and there. now, she NEVER forgets it, she says

she knows for sure she's getting better now - sometime after she passed

the 3mo. mark, which would have been about may 9th.

i know of 3 people having a hard time with the TF, and i haven't asked

for permission to use their names, so i'm not :

one who started the study last august, and was on this list at one time

- don't know if she still is. she believes it made her worse and put

her in the hospital (pain). she went off it and hasn't gone back on,

since (i dunno if she's talked to dr since then - i need to talk to her

& find out.)

another - on it also since it first went on sale beginning of february -

she also had FM to start with, and it got worse. she stuck it out (her

daughter, ill for 2 yrs, went skiing after 2-3 wks on it). found out

from HEMEX testing she had one of the genetic factors for hypercoag (her

daughter doesn't). she tried a month on heparin and got sick from it.

is waiting to try something else, but is still on/never went off the TF.

she is having some increased energy, can drive some now, and shop in the

front of the store - can't make it to the back isles yet :-). but is

still in a lot of pain. anyway, the point i'm being so long winded in

making (sorry) is the dr said the TF will still work, but it will take

longer when the " pipes are clogged " . she's supposed to be trying

something else, after it's tried first on a local patient.

the third person is a friend of the last one - i've heard she's having a

similarly hard time with it.

my story so far (i'm on day 74 of 3 capsules a day), as briefly as

possible, the first 4 weeks were so-so, including periods where i just

wanted to sleep 24/7 (2-3 days at a time), feeling of feverishness,

minor aches and pains (i've had cfs/me since 1980 - have never had much

in the way of FM type pain), lots of stiffness/minor pain in feet and

fingers. (i did though, feel a little more energy by the 2nd or 3rd

week.)

then there was 3wks kinda' yuchy, that were kicked off by taking 6

bromelains on the first day LOL (i haven't taken it since, would work up

slowly on it, if i thought i would remember to take it regularly :-/ -

lymph glands so swollen & tender - i could hardly turn my head) .....

have had increased perspiration & odor (all 3 of us!)

after that three weeks - i woke up one morning, and just suddenly felt a

little better - like the " clouds were lifting " . still had the minor

ache, pain, & stiffness - but i felt very " different " - dunno how to

describe it . . .

i've been playing " taxi service " , and doing quite a bit of errand

running, etc., stuff that should have put me horizontal for 2 or 3

days...... after 1/2 day of it - let alone 2-3 days in a row of it. i

get very tired - but am not so bad that i can't get up the next day.

yesterday, i probably spent a total of 4hrs on my feet - shopping,

cooking, and cleaning up. i was extremely tired last night, more so

than i've been in quite a while (cause i know better) - but i was able

to get up today - i still felt tired from yesterday, but i wasn't

immobile, and i shoulda' been . . .

a couple nights ago i had the sensation, for a brief period, of feeling

" normal " , very strange, brain & sinuses clear - or at least as normal as

i've felt since before my daughter was born in '86. geez, i was

thinking about my resume.....

i've noticed the last few days that the pain/stiffness in fingers is

letting up. also, when i was cooking/cleaning yesterday, i was doing it

with the radio on, and it didn't drive me to distraction....

@}{~{<<~~~~~~~~~~~~~~~~~~~~

debbie s. - dlsherman@...