Jump to content
RemedySpot.com

Peanut Butter Question

Rate this topic


Guest guest

Recommended Posts

Guest guest

For those of you who make your own peanut butter from

scratch, how do you make it?

I tried making it for the 1st time and it did not

meet my expectations – it never got to the paste stage in my mini

processor. I roasted about a pound of unshelled, raw peanuts at 350 degrees for

30 min. I let them cool, then hand shucked them. Today one of my hands hurt so

is it ok to start out with shelled raw nuts?

Even though I roasted them (in the shell) the peanuts were

still very pale in color – not the darker brown of commercial brands. Should

they be roasted longer to attain a darker color? Is that even desirable?

I whizzed up 1 1/2 cups peanuts in my mini processor with 2 ½

tablespoons of safflower oil. This apparently was not enough oil. What

proportions do you use? I am planning on buying peanut oil to add to my next

batch.

I added a few pinches of salt also. It’s very good,

just grainy and not holding together, especially after refrigeration. This is

the first time in 5 years that I wanted to try peanut butter again. Thankfully

I am tolerating it just fine! Now I just need to learn how to make it. Thanks

in advance for any culinary help!

Carol

CD 22 yrs  SCD 5 yrs

Link to comment
Share on other sites

Guest guest

Hey Carol,

I would shell them first, THEN roast them. The whole point is to brown the

peanut and impart that flavor on it, then grind it.

Secondly, the grainding process should be done in a high powered blender of some

sort. I have a Vita-mix and that works just fine, but of course, those things

have lawn mower type motors in them. Try adding an additional extra oily nut

like roasted pine nuts. THat'll add some great flavor.

good luck, hope that helps!

jonathan

Link to comment
Share on other sites

Guest guest

Hey Carol,

I would shell them first, THEN roast them. The whole point is to brown the

peanut and impart that flavor on it, then grind it.

Secondly, the grainding process should be done in a high powered blender of some

sort. I have a Vita-mix and that works just fine, but of course, those things

have lawn mower type motors in them. Try adding an additional extra oily nut

like roasted pine nuts. THat'll add some great flavor.

good luck, hope that helps!

jonathan

Link to comment
Share on other sites

Guest guest

Thanks ! The pine nuts sound like the perfect addition!

Maybe I need to hook up a 2 stroke engine to my mini processor…

Carol

CD 22 yrs SCD 5 yrs

From:

BTVC-SCD [mailto:BTVC-SCD ] On Behalf Of

I would shell them first, THEN roast them. The

whole point is to brown the peanut and impart that flavor on it, then grind it.

Secondly, the grainding process should be done in a high powered blender of

some sort. I have a Vita-mix and that works just fine, but of course, those

things have lawn mower type motors in them. Try adding an additional extra oily

nut like roasted pine nuts. THat'll add some great flavor.

Link to comment
Share on other sites

Guest guest

Carol

I

have been making my own peanut butter since my early days on SCD. I

usually purchase peanuts that are roasted in the shell, shell them, throw them

in my food processor with a bit of salt, and start processing. I rarely

need to add any oil. But it can take 10 to 15 minutes of processing in my

food processor (Cuisinart) before the nuts turn into butter. I run the

processor for about 5 minutes, then let it rest for 5 minutes or so to let the

motor cool down, then repeat as needed until the butter is the right

consistency. I do keep the peanut butter in the fridge, so the oils

usually don’t separate out, although it isn’t a problem to stir

again.

I’ve

also purchased raw, shelled peanuts and then roasted them in my oven, added a

bit of salt, then dumped them into my food processor. I always feel a bit

suspicious of the processor, however, so I tend to pick up the

roasted-in-the-shell, unsalted peanuts if I have a choice. I have just

tried a batch of roasted, unsalted, shelled peanuts from the same company where

I get my pecan meal, and so far haven’t felt any reaction, so I might use

this source more often. Saves a lot of time shelling peanuts

[grin].

I

would guess that a mini-processor doesn’t have the power to turn the

peanuts into butter. You might need to invest in a food processor; this and

my juicer are the only “gadgets” I use regularly in preparing SCD

meals. I make nut flour in the food processor, as well as peanut butter,

and it certainly chops up some ingredients quickly. Lots of people also mix up

their nut flour muffins and breads in a food processor, although I prefer

mixing that type of batter by hand.

And

you do need to let the peanuts process for a while, longer than you expect to at

first.

Kim M.

SCD 6 years

Sphincter of Oddi dysfunction 6+ years

neurological & spinal deterioration 3+ years

>>>>>>>>>>>>>>>>>>>>>>

For

those of you who make your own peanut butter from scratch, how do you

make it?

Link to comment
Share on other sites

Guest guest

i'm shocked! you tolerate peanut butter Kim??? with the yeast and it being so

hard to digest i am just so surprised - and pyched for my own future!! LOL

eileen

2 years 5 months scd

-- In BTVC-SCD , " Kim Mumbower " wrote:

>

> Carol

>

>

>

> I have been making my own peanut butter since my early days on SCD. I

> usually purchase peanuts that are roasted in the shell, shell them, throw

> them in my food processor with a bit of salt, and start processing. I

> rarely need to add any oil. But it can take 10 to 15 minutes of processing

> in my food processor (Cuisinart) before the nuts turn into butter. I run the

> processor for about 5 minutes, then let it rest for 5 minutes or so to let

> the motor cool down, then repeat as needed until the butter is the right

> consistency. I do keep the peanut butter in the fridge, so the oils usually

> don't separate out, although it isn't a problem to stir again.

>

>

>

> I've also purchased raw, shelled peanuts and then roasted them in my oven,

> added a bit of salt, then dumped them into my food processor. I always feel

> a bit suspicious of the processor, however, so I tend to pick up the

> roasted-in-the-shell, unsalted peanuts if I have a choice. I have just

> tried a batch of roasted, unsalted, shelled peanuts from the same company

> where I get my pecan meal, and so far haven't felt any reaction, so I might

> use this source more often. Saves a lot of time shelling peanuts [grin].

>

>

>

> I would guess that a mini-processor doesn't have the power to turn the

> peanuts into butter. You might need to invest in a food processor; this and

> my juicer are the only " gadgets " I use regularly in preparing SCD meals. I

> make nut flour in the food processor, as well as peanut butter, and it

> certainly chops up some ingredients quickly. Lots of people also mix up

> their nut flour muffins and breads in a food processor, although I prefer

> mixing that type of batter by hand.

>

>

>

> And you do need to let the peanuts process for a while, longer than you

> expect to at first.

>

>

>

> Kim M.

>

> SCD 6 years

>

> Sphincter of Oddi dysfunction 6+ years

>

> neurological & spinal deterioration 3+ years

>

>

>

> >>>>>>>>>>>>>>>>>>>>>>

>

> For those of you who make your own peanut butter from scratch, how do you

> make it?

>

Link to comment
Share on other sites

Guest guest

I'm with you Eileen. Peanut butter does baaaadddd things to me!

> >

> > Carol

> >

> >

> >

> > I have been making my own peanut butter since my early days on SCD. I

> > usually purchase peanuts that are roasted in the shell, shell them, throw

> > them in my food processor with a bit of salt, and start processing. I

> > rarely need to add any oil. But it can take 10 to 15 minutes of processing

> > in my food processor (Cuisinart) before the nuts turn into butter. I run the

> > processor for about 5 minutes, then let it rest for 5 minutes or so to let

> > the motor cool down, then repeat as needed until the butter is the right

> > consistency. I do keep the peanut butter in the fridge, so the oils usually

> > don't separate out, although it isn't a problem to stir again.

> >

> >

> >

> > I've also purchased raw, shelled peanuts and then roasted them in my oven,

> > added a bit of salt, then dumped them into my food processor. I always feel

> > a bit suspicious of the processor, however, so I tend to pick up the

> > roasted-in-the-shell, unsalted peanuts if I have a choice. I have just

> > tried a batch of roasted, unsalted, shelled peanuts from the same company

> > where I get my pecan meal, and so far haven't felt any reaction, so I might

> > use this source more often. Saves a lot of time shelling peanuts [grin].

> >

> >

> >

> > I would guess that a mini-processor doesn't have the power to turn the

> > peanuts into butter. You might need to invest in a food processor; this and

> > my juicer are the only " gadgets " I use regularly in preparing SCD meals. I

> > make nut flour in the food processor, as well as peanut butter, and it

> > certainly chops up some ingredients quickly. Lots of people also mix up

> > their nut flour muffins and breads in a food processor, although I prefer

> > mixing that type of batter by hand.

> >

> >

> >

> > And you do need to let the peanuts process for a while, longer than you

> > expect to at first.

> >

> >

> >

> > Kim M.

> >

> > SCD 6 years

> >

> > Sphincter of Oddi dysfunction 6+ years

> >

> > neurological & spinal deterioration 3+ years

> >

> >

> >

> > >>>>>>>>>>>>>>>>>>>>>>

> >

> > For those of you who make your own peanut butter from scratch, how do you

> > make it?

> >

>

Link to comment
Share on other sites

Guest guest

I got a little crazy a couple months ago and ate about 1/2 cup of peanut butter

twice in one week. I went into a flare that I'm still coming out of (eating

beans this week didn't help UGH). Peanut butter is the devil. I'm sure of it!!!

:P

Misty Kimble

CD - no meds

SCD - 2 + years

> >

> > i'm shocked! you tolerate peanut butter Kim??? with the yeast and it being

so hard to digest i am just so surprised - and pyched for my own future!! LOL

Link to comment
Share on other sites

Guest guest

and i was such an addict for years!!!!!!!!!!!! it's so hard to digest :(

eileen

> > >

> > > i'm shocked! you tolerate peanut butter Kim??? with the yeast and it being

so hard to digest i am just so surprised - and pyched for my own future!! LOL

>

Link to comment
Share on other sites

Guest guest

Eileen

You

know my body does the opposite of what is expected [grin]. I can’t touch

a nut butter but do fine with a small amount of peanut butter. I could

tolerate peanut butter from the 2nd week on SCD, but severely

limited how often I had it and kept the amount tiny during my first 2 years on

SCD because of my candida overgrowth. I don’t get many cravings, but

peanut butter is one of the few (walnuts and hard-boiled eggs are the other two),

so I figured out the bare minimum I could eat and not experience a yeast

surge.

I

still don’t eat much peanut butter or have it often (triggers nausea) but

my body seems to require it. I found my body reacted to all commercial peanut

butters, even when the only ingredients listed were peanuts and salt, so I

learned to make my own.

Kim M.

SCD 6 years

Sphincter of Oddi dysfunction 6+ years

neurological & spinal deterioration 3+ years

>>>>>>>>>>>>>>>>>>>>>

i'm

shocked! you tolerate peanut butter Kim??? with the yeast and it being so hard

to digest i am just so surprised - and pyched for my own future!! LOL

eileen

2 years 5 months scd

Link to comment
Share on other sites

Guest guest

i am usually the odd man out -lol - i wonder if i can tolerate it and i'm just

too scared?? though 1 of my kids throat will close, so maybe not something i

should attempt ever again anyway :-)

thanks

eileen

>

> Eileen

>

>

>

> You know my body does the opposite of what is expected [grin]. I can't

> touch a nut butter but do fine with a small amount of peanut butter. I

> could tolerate peanut butter from the 2nd week on SCD, but severely limited

> how often I had it and kept the amount tiny during my first 2 years on SCD

> because of my candida overgrowth. I don't get many cravings, but peanut

> butter is one of the few (walnuts and hard-boiled eggs are the other two),

> so I figured out the bare minimum I could eat and not experience a yeast

> surge.

>

>

>

> I still don't eat much peanut butter or have it often (triggers nausea) but

> my body seems to require it. I found my body reacted to all commercial

> peanut butters, even when the only ingredients listed were peanuts and salt,

> so I learned to make my own.

>

>

>

> Kim M.

>

> SCD 6 years

>

> Sphincter of Oddi dysfunction 6+ years

>

> neurological & spinal deterioration 3+ years

>

>

>

> >>>>>>>>>>>>>>>>>>>>>

>

> i'm shocked! you tolerate peanut butter Kim??? with the yeast and it being

> so hard to digest i am just so surprised - and pyched for my own future!!

> LOL

> eileen

> 2 years 5 months scd

>

Link to comment
Share on other sites

Guest guest

I

don’t think it is such a good idea to have peanut butter around your

house if one of your children reacts severely to it. Sometimes just the

presence of a food in the vicinity can trigger a severe allergic response for

those individuals particularly sensitive to it. Risky even though you are

the only one eating the peanut butter.

This

might be something you can try, one day, if you feel adventurous, when you are

out somewhere [grin]. Or not! There are plenty of people who

eat well on SCD without peanuts or peanut butter [grin].

Kim M.

SCD 6 years

>>>>>>>>>>>>>>>>>>>>>>>.

i

am usually the odd man out -lol - i wonder if i can tolerate it and i'm just

too scared?? though 1 of my kids throat will close, so maybe not something i

should attempt ever again anyway :-)

thanks

eileen

Link to comment
Share on other sites

Guest guest

i agree!!

eileen

>

> I don't think it is such a good idea to have peanut butter around your house

> if one of your children reacts severely to it. Sometimes just the presence

> of a food in the vicinity can trigger a severe allergic response for those

> individuals particularly sensitive to it. Risky even though you are the

> only one eating the peanut butter.

>

>

>

> This might be something you can try, one day, if you feel adventurous, when

> you are out somewhere [grin]. Or not! There are plenty of people who eat

> well on SCD without peanuts or peanut butter [grin].

>

>

>

> Kim M.

>

> SCD 6 years

>

>

>

> >>>>>>>>>>>>>>>>>>>>>>>.

>

> i am usually the odd man out -lol - i wonder if i can tolerate it and i'm

> just too scared?? though 1 of my kids throat will close, so maybe not

> something i should attempt ever again anyway :-)

> thanks

> eileen

>

Link to comment
Share on other sites

Guest guest

I doubt you would tolerate it Eileen! I once read a good test to see it you

have yeast is to eat a little PB and wait for some discomfort. I tried it,

twice(had to confirm it, LOL)- both times lots of discomfort that lasted 24 hrs.

> >

> > Eileen

> >

> >

> >

> > You know my body does the opposite of what is expected [grin]. I can't

> > touch a nut butter but do fine with a small amount of peanut butter. I

> > could tolerate peanut butter from the 2nd week on SCD, but severely limited

> > how often I had it and kept the amount tiny during my first 2 years on SCD

> > because of my candida overgrowth. I don't get many cravings, but peanut

> > butter is one of the few (walnuts and hard-boiled eggs are the other two),

> > so I figured out the bare minimum I could eat and not experience a yeast

> > surge.

> >

> >

> >

> > I still don't eat much peanut butter or have it often (triggers nausea) but

> > my body seems to require it. I found my body reacted to all commercial

> > peanut butters, even when the only ingredients listed were peanuts and salt,

> > so I learned to make my own.

> >

> >

> >

> > Kim M.

> >

> > SCD 6 years

> >

> > Sphincter of Oddi dysfunction 6+ years

> >

> > neurological & spinal deterioration 3+ years

> >

> >

> >

> > >>>>>>>>>>>>>>>>>>>>>

> >

> > i'm shocked! you tolerate peanut butter Kim??? with the yeast and it being

> > so hard to digest i am just so surprised - and pyched for my own future!!

> > LOL

> > eileen

> > 2 years 5 months scd

> >

>

Link to comment
Share on other sites

Guest guest

The TJ's raw almond butter (skins on) I *was* eating made me nauseous, too! If I

ate more than a few tsps at a time, that is. Is that a common reaction among

SCDers with nut butters? Interesting!

Thanks,

W.

Lymphocytic (not Ulcerative) colitis 2.5 years

Gluten and cow's milk intolerance (Enterolab)

SCD 1 month

Entocort 6mg/day

1/2 Imodium/day

>

>

>

> I still don't eat much peanut butter or have it often (triggers nausea) but

> my body seems to require it. I found my body reacted to all commercial

> peanut butters, even when the only ingredients listed were peanuts and salt,

> so I learned to make my own.

> Kim M.

>

> SCD 6 years

>

> Sphincter of Oddi dysfunction 6+ years

>

> neurological & spinal deterioration 3+ years

Link to comment
Share on other sites

Guest guest

I don't think it is such a good idea to have peanut butter around your house

if one of your children reacts severely to it. Sometimes just the presence

of a food in the vicinity can trigger a severe allergic response for those

individuals particularly sensitive to it. Risky even though you are the

only one eating the peanut butter.

I would agree with this. My sister has, and always has had, a

terrible reaction to crab. She gets monster hives. Once as an adult

she was visiting Mama and got the crab hives only Mama certainly

wasn't serving crab. But she finally remembered she had fixed

herself some 2-3 days before and the only place it could have

possibly bin was in the air or a bit on the dish rag. My sister was

just as sick as if she'd eaten some. And of course the peanut butter

can be a really bad reaction, too.

Link to comment
Share on other sites

Guest guest

You're pretty new at SCD, so that's most likely the reason. Also, the raw almond

butter is not smooth like the roasted, so I wouldn't be surprised if it was more

difficult to digest. Personally, I don't like the texture of the raw and stick

to roasted for that very reason.

Holly

Crohn's

SCD 12/01/08

> >

>

> >

> >

> > I still don't eat much peanut butter or have it often (triggers nausea) but

> > my body seems to require it. I found my body reacted to all commercial

> > peanut butters, even when the only ingredients listed were peanuts and salt,

> > so I learned to make my own.

> > Kim M.

> >

> > SCD 6 years

> >

> > Sphincter of Oddi dysfunction 6+ years

> >

> > neurological & spinal deterioration 3+ years

>

Link to comment
Share on other sites

Guest guest

I got nauseous the first few times I ate almond butter with the skins one. If I

go a long time without eating it, it will still happen sometimes. I still eat it

though. It only lasts a few seconds then I can finish it. When I break down and

eat some, it's because I'm craving it so bad that I can't think of anything

else. So, for me, it's worth it though it might not be the best thing for me.

<grin>

One day I'll break down and buy Almondie but my problem is I have no self

control and will end up eating the whole jar in a few days.

Misty Kimble

CD - no meds

SCD - 2 + years

>

> The TJ's raw almond butter (skins on) I *was* eating made me nauseous, too! If

I ate more than a few tsps at a time, that is. Is that a common reaction among

SCDers with nut butters? Interesting!

>

> Thanks,

> W.

> Lymphocytic (not Ulcerative) colitis 2.5 years

> Gluten and cow's milk intolerance (Enterolab)

> SCD 1 month

> Entocort 6mg/day

> 1/2 Imodium/day> >

> > SCD 6 years

Link to comment
Share on other sites

Guest guest

There's nothing like Almondie.  It's so sweet and smooth.  Very small container thank goodness.  I won't order it again for awhile.  I received one jar with some jam as a gift from DW (my mom ordered it for me and she got dried fruit mix when we ordered something else there).  It is awesome.  I don't think you can duplicate it at home.  It said something about cold pressed, skinless almonds.  I haven't even thought about buying Marantha or one of those since I've had the almondie.  I do like to toast pecans sometimes and make butter but I don't tolerate very much so rarely make it.

 

Debbie 41 cd

 

I got nauseous the first few times I ate almond butter with the skins one. If I go a long time without eating it, it will still happen sometimes. I still eat it though. It only lasts a few seconds then I can finish it. When I break down and eat some, it's because I'm craving it so bad that I can't think of anything else. So, for me, it's worth it though it might not be the best thing for me. <grin>

One day I'll break down and buy Almondie but my problem is I have no self control and will end up eating the whole jar in a few days. Misty KimbleCD - no medsSCD - 2 + years

>> The TJ's raw almond butter (skins on) I *was* eating made me nauseous, too! If I ate more than a few tsps at a time, that is. Is that a common reaction among SCDers with nut butters? Interesting!

> > Thanks,> W.> Lymphocytic (not Ulcerative) colitis 2.5 years> Gluten and cow's milk intolerance (Enterolab)> SCD 1 month> Entocort 6mg/day> 1/2 Imodium/day> >

> > SCD 6 years

Link to comment
Share on other sites

Guest guest

it's pecan for me then - maybe i'll do almond soon??

thanks

eileen

> > >

> > > Eileen

> > >

> > >

> > >

> > > You know my body does the opposite of what is expected [grin]. I can't

> > > touch a nut butter but do fine with a small amount of peanut butter. I

> > > could tolerate peanut butter from the 2nd week on SCD, but severely

limited

> > > how often I had it and kept the amount tiny during my first 2 years on SCD

> > > because of my candida overgrowth. I don't get many cravings, but peanut

> > > butter is one of the few (walnuts and hard-boiled eggs are the other two),

> > > so I figured out the bare minimum I could eat and not experience a yeast

> > > surge.

> > >

> > >

> > >

> > > I still don't eat much peanut butter or have it often (triggers nausea)

but

> > > my body seems to require it. I found my body reacted to all commercial

> > > peanut butters, even when the only ingredients listed were peanuts and

salt,

> > > so I learned to make my own.

> > >

> > >

> > >

> > > Kim M.

> > >

> > > SCD 6 years

> > >

> > > Sphincter of Oddi dysfunction 6+ years

> > >

> > > neurological & spinal deterioration 3+ years

> > >

> > >

> > >

> > > >>>>>>>>>>>>>>>>>>>>>

> > >

> > > i'm shocked! you tolerate peanut butter Kim??? with the yeast and it being

> > > so hard to digest i am just so surprised - and pyched for my own future!!

> > > LOL

> > > eileen

> > > 2 years 5 months scd

> > >

> >

>

Link to comment
Share on other sites

Guest guest

I loved the Almondie when I ordered a jar some months ago. But it IS

expensive! I have wondered if I could make my own at least somewhat

cheaper from my blanched sliced almonds. I need to try, and see if I

can approximate the cost.

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...