Monday, March 30, 2015

[Healthy_Recipes_For_Diabetic_Friends] Hummus - 11g Carbs, 3g Fiber From: DrWeil.com

 

Hummus - 11g Carbs, 3g Fiber

From: DrWeil.com
This wonderful bean spread has gained in popularity over the past few years. Our version has all the benefits of a more traditional recipe, but with less olive oil. The combination of garbanzo beans (also called chickpeas), tahini, lemon juice, cumin and garlic is a show-stopper. This is wonderful as a sandwich spread or as a dip with raw vegetables or pita triangles. Keep a batch in your refrigerator all the time and you'll never be without a nutritious snack or lunch.
Servings: 10

1 3/4 cups dried chickpeas (garbanzos)
1 tsp baking soda
1/2 cup sesame tahini
1/4 cup cold water
1/4 cup fresh lemon juice
1/2 tsp ground cumin
3 - 4 cloves garlic, mashed
1 Tbsp quality extra-virgin olive oil

1. Soak the chickpeas for 8 hours with the baking soda in cold water to cover.

2. Bring the chickpeas to a boil over high heat, reduce heat, cover, and cook until soft, about 45 minutes. Drain, reserving a bit of the liquid.

3. Make the tahini sauce: Blend in a food processor or blender the tahini, cold water, lemon juice, cumin, and garlic. Measure out 1/2 cup of this sauce for the hummus, saving the rest.

4. Put the drained chickpeas in a food processor and process to a rough puree, adding a little of the cooking liquid if necessary. The mixture should not be totally smooth. Add the tahini sauce and process until just mixed.

5. Scrape the mixture into a bowl. Stir in the olive oil.

6. Serve with pita bread, whole-grain crackers, or carrot sticks.

Servings: 10
Nutrition per Serving: 102 Calories, 5g Total Fat, 1g Sat,0mg Cholesterol, 4g Protein, 150mg Sodium, 11g Carbs, 3g Fiber


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Posted by: chefgloria1030@yahoo.com
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[Healthy_Recipes_For_Diabetic_Friends] Angel Almond Cookies

 

Angel Almond Cookies

(Each cookie has 4 Net Carbs when using Whey Low)

2 egg whites
2/3 cup sugar (I use Whey Low)
1 1/2 cups ground almond meal
1/4 tsp almond extract
1/4 tsp vanilla extract
1/8 tsp salt
20 whole almonds

Preheat oven to 375 degrees F. Line 2 baking sheets with parchment paper or foil and lightly coat with cooking spray.

In a large bowl, beat egg whites until doubled. Add sugar and whisk just until combined. Fold in almond meal, almond extract, vanilla extract, and salt until thoroughly combined. Place a spoonful of dough on parchment paper and place an almond in the center of dough; press down lightly. Repeat until all dough is used. Bake 10 to 12 minutes, or until golden brown.

Let cool on a wire rack before serving. Makes: 20 Notes: If you love almond flavor as much as we do, you'll just love our Almond Crusted Brie!

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Posted by: Darlene BC <dsharple@shaw.ca>
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Sunday, March 29, 2015

Re: [epilepsy] hi erin back here

 

Erin,

Hang in there. I can understand what you're going through.  I started having gran mal seizures at the age of 34 for no apparent reason. It took four years to find a doctor who didn't go by how typical patients responded because I didn't. If you and your doctor don't know why you're having seizures, find another doctor.
Your body is your responsibility; your doctor recommends.

Paul


On Thu, Mar 26, 2015 at 4:06 PM, Erin nichole p misty58001@hotmail.com [epilepsy] <epilepsy@yahoogroups.com> wrote:
 

Well i am feeling very depressed my dr is upping my lamictal from 200 to 400.I am very anxious about it.frustrated my dr has down the eeg,ekg and mri and of course nothing is wrongEmoji


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Posted by: <pmwpaul@gmail.com>
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Re: [epilepsy] MMJ discussion

 

Christopher,

PLANET EARTH CALLING!!!
NOT ALL ANTI-SEIZURE MEDICATIONS WORK FOR EVERYBODY!!!

What works for some people, works.  What doesn't work for some people, doesn't.

If something might help me with my epilepsy, I'm willing to talk and research it. If it doesn't work for you that doesn't give you the right to dictate what I can talk about and research.

Paul

On Fri, Mar 13, 2015 at 5:49 PM, Christopher Range lcms0516@comcast.net [epilepsy] <epilepsy@yahoogroups.com> wrote:
 

I am sick of how this discussion has verged on suggesting others' take
it for their epilepsy!!!!!!!! It doesn't work for everyone!!!! So stop
promoting it!!!!!

I don't care if I get kicked out of the group, or not!!! The mere fact
that this discussion is continuing, says to me that the moderator(s)
don't care about the promotion of a drug that doesn't work for everyone!!!!!

Christopher


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Posted by: <pmwpaul@gmail.com>
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RE: [epilepsy] Filming The Walk

 

Thank you Pat.

I have applied to and received an acceptance from Kickstarter already. It unfortunately can take up to a week before being actually placed on the site. We will see if it gets opened in time. I do have some people waiting so there will be some action right away which they say makes a big difference in people even recognizing it is there.


My other concern is if the foundation will allow me to set up a 6-8 foot table somewhere for equipment and promotion and to set up the camera on a tripod to film some of the interviews. I also hope to walk with everyone and interview with the camera handheld. My goal is at least 150 stories to edit down to a 58 minute film which is the time required by public television. If the stories are incredible enough along with the B-Roll I hope to film the day before and after. And I can possibly obtain Overhead footage from the newsteams' helicopter shots I may have something intriguing enough to build to a 68-90 minute for festivals around the world.


I will also send out a request for peoples personal poetry and music for Voice Over and back-up from around the country and possibly the world.



Sam.

(847)361-4786

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Posted by: ambimind65@yahoo.com
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Saturday, March 28, 2015

RE: [epilepsy] hi erin back here

 

Erin

 

My son was at college in Tyler, Texas.  The neurologist (just moved to the area from out of state) took him off of Lamictal and put him on Depakote.  Advised me it would make him hyper (when in fact it does not – it is the opposite)  The nurses played games with me on the phone by putting all my calls on hold for hours.  They thought it was funny

 

Another doctor (very fine doctor) – his main admin thought she was god and made decisions without his input.

 

I will not get into the details other than to say; Know your doctor, the nurses and admin; know yourself; stay abreast and know what is going on – you have to know your body best

 

H

 

 

 

 

 

From: epilepsy@yahoogroups.com [mailto:epilepsy@yahoogroups.com]
Sent: Thursday, March 26, 2015 4:52 PM
To: epilepsy@yahoogroups.com
Subject: Re: [epilepsy] hi erin back here

 

 

I've been there where a couple of years ago my old neurologist had me so overdosed on medication I was seeing double, and he would not listen where finally I had to go to an ophthalmologist where he found issues where he sent me to a neuropsychologist where he wrote a letter to my neurologist these issues of being overdosed although the next appointment I went to him he totally denied he did any such things.  Immediately after that I was out of his office to a new neurologist where he's more helped me in two years than the whole time I was a at my old neurologist.  Pretty much depending on your doctor can you trust him or her their decisions of increasing your medication.

Sent from my iPhone


On Mar 26, 2015, at 5:06 PM, Erin nichole p misty58001@hotmail.com [epilepsy] <epilepsy@yahoogroups.com> wrote:

 

Well i am feeling very depressed my dr is upping my lamictal from 200 to 400.I am very anxious about it.frustrated my dr has down the eeg,ekg and mri and of course nothing is wrong

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Posted by: HPCJr21 <hpcjr21@gmail.com>
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RE: [epilepsy] my medication

 

Hi Robert

Sorry you had so many issues with tegretol, I had to go the other way as I got older and slightly heavier, 1100 is the maximum I can take1200 makes me feel ill, very drowsy. I am on 500 mg of ceppra too, I take 600 mg tegretol morning and 500 at night and the ceppra is split evenly. Yes I don't know the french braille system but I am sure the braille on the boxes does not include the doses, I will double check though, the french and uk braille is totally different so have to learn the french system but won't bother now. I will be returning to live in the uk this year so once I have used my stock of square boxes I will be put on to the other boxes I assume. I don't like to run out of my medication. I have to have a blood test for the tegretol once a year, it is about due. But will leave it this year until just before I return so I have up to date papers.

Regards

Adrien

-----Original Message-----
From: epilepsy@yahoogroups.com [mailto:epilepsy@yahoogroups.com]
Sent: Saturday, March 28, 2015 1:06 AM
To: epilepsy@yahoogroups.com
Subject: RE: [epilepsy] my medication

I take 900mg/day. I used to take much more but had side effect problems, especially double vision at 1400mg. I was OK at 1200mg. Then it needed to be lowered as my blood counts were still not recovering. I went to 1100mg then 1000mg and I stuck there for some years. I had started to take the meds three times a day in an effort to reduce the double vision, which worked a bit to reduce the worst of it. So at 1000mg I was supplied with 400mg tabs to take morning and night and 200mg to take midday. I then asked if I could reduce to 900mg to try to reduce some of the early morning sedation (part of which was due to Mysoline it has to be said) so to start off with I simply snapped a 200mg tablet for midday. Later I was issued with 100mg Tegretol (ordinary Tegretol) and I just take that at midday with the 400mg Tegretol Prolonged Release morning and night.

I have noticed there is Braille on boxes but didn't know this fails to include dose.

In recent times, maybe for a year now, I have been issued with the proper UK issue packs of 56 Tegretol Prolonged Release. I think this must be something to do with the pound to euro exchange rate. Maybe it was cheaper to buy in parallel imports back along and relabel and now it isn't!

Rob

From: epilepsy@yahoogroups.com [mailto:epilepsy@yahoogroups.com]
Sent: 26 March 2015 15:51
To: epilepsy@yahoogroups.com
Subject: RE: [epilepsy] my medication

Hi Robert

This is interesting as I have to break my tegretol especially the 200 mg tablets as I only need to take 1100 mg a day, the doctor gave me 1200 but I find that too much, it makes me feel ill. The 1100 is sufficient along with my ceppra. You evidently get the same boxes as I get here in France, I just wish they would put in braille the dosage on the box along with the name, they are pretty good here though as most drugs do have braille on them.

Regards

Adrien

.

<http://geo.yahoo.com/serv?s=97359714/grpId=8819/grpspId=1705061677/msgId=65835/stime=1427474990>
<http://y.analytics.yahoo.com/fpc.pl?ywarid=515FB27823A7407E&a=10001310322279&js=no&resp=img>

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Posted by: <salamander22160@gmail.com>
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RE: [epilepsy] Filming The Walk

 

Consider a website at www.kickstarter.com or another crowd funding site. This one is geared more toward your goals. “Kickstarter is the world's largest funding platform for creative projects. A home for film, music, art, theater, games, comics, design, photography, and more.”

 

Pat D


From: epilepsy@yahoogroups.com [mailto:epilepsy@yahoogroups.com]
Sent: Friday, March 27, 2015 9:03 AM
To: epilepsy@yahoogroups.com
Subject: [epilepsy] Filming The Walk

 

 

Hello. I am a Documentary Filmmaker with uncontrolled seizures for 18ys. I have been searching for 2 years for funds to produce a documentary where I will interview people re-calling their most memorable attack in public. The type of attack and the awareness, knowledge, reactions etc. of the public around them. I can obtain all the interviews and B-Roll necessary at the Walk on April 11. Where can I go for donations to cover the costs of flying myself, my interviewee (who has had seizures her whole life, uncontrolled) and my cinematographer along with 3 nights in a hotel. Sam.    Ambitious Minds Productions

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Posted by: "Aina & Pat DeLorenzo" <Aina-Pat@cox.net>
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Re: [epilepsy] How-many members from this: list, are from?

Hello Canada,

smiles: what time is it their-now?

-----

)-----Original Message-----
From: Mirek Kotis kotismjr@hotmail.com [epilepsy] - Email Address: epilepsy@yahoogroups.com
Sent On: 3/28/2015 10:06
Sent To: epilepsy@yahoogroups.com - Email Address: epilepsy@yahoogroups.com
subject: Re: [epilepsy] How-many members from this: list, are from?

Not me…. Beautiful British Colombia Canada here
Mirek Kotis


Sent from Windows Mail

From: epilepsy@yahoogroups.com
Sent: ?Friday?, ?March? ?27?, ?2015 ?2?:?09? ?PM
To: epilepsy@yahoogroups.com




I'm from Lansing Michigan USA

Joseph
--------------------------------------------
On Tue, 3/24/15, Tammy Mccoy Uniquepnk@tds.net [epilepsy] <epilepsy@yahoogroups.com> wrote:

Subject: Re: [epilepsy] How-many members from this: list, are from?
To: epilepsy@yahoogroups.com
Date: Tuesday, March 24, 2015, 8:56 PM

I am from USA.

Tammy

----- Original Message -----
From: "'Nelson F. Vega' carebear40@bellsouth.net
[epilepsy]" <epilepsy@yahoogroups.com>
To: Epilepsy@yahoogroups.com
Sent: Tuesday, March 24, 2015 7:46:42 PM
Subject: [epilepsy] How-many members from this: list, are
from?

Are you listers-from the USA?
I am...

Nelson F. Vega


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Re: [epilepsy] How-many members from this: list, are from?

 

Not me…. Beautiful British Colombia Canada here

Mirek Kotis

Sent from Windows Mail

From: epilepsy@yahoogroups.com
Sent: ‎Friday‎, ‎March‎ ‎27‎, ‎2015 ‎2‎:‎09‎ ‎PM
To: epilepsy@yahoogroups.com

 

I'm from Lansing Michigan USA

Joseph
--------------------------------------------
On Tue, 3/24/15, Tammy Mccoy Uniquepnk@tds.net [epilepsy] <epilepsy@yahoogroups.com> wrote:

Subject: Re: [epilepsy] How-many members from this: list, are from?
To: epilepsy@yahoogroups.com
Date: Tuesday, March 24, 2015, 8:56 PM

I am from USA.

Tammy

----- Original Message -----
From: "'Nelson F. Vega' carebear40@bellsouth.net
[epilepsy]" <epilepsy@yahoogroups.com>
To: Epilepsy@yahoogroups.com
Sent: Tuesday, March 24, 2015 7:46:42 PM
Subject: [epilepsy] How-many members from this: list, are
from?

Are you listers-from the USA?
I am...

Nelson F. Vega






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Posted by: Tammy Mccoy <uniquepnk@tds.net>
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    epilepsy-fullfeatured@yahoogroups.com



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Posted by: Mirek Kotis <kotismjr@hotmail.com>
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Friday, March 27, 2015

Re: [epilepsy] Seizure Types

 


I am not sure the name but think there is one called Epilepsy.com.

 

I have no warning. I'm not sure the name of what I have, some doctors think it is non-epileptic seizures (psuedoseizures as some call them).  But I disagree.  I think that even if stress increases them, they would show up on EEGs and are epileptic.  And since I don't fall, I see that as something to be grateful for.  Fibromyalgia is harder to live with.

 

Oh well, life goes on and as I said I don't know what type they are. I don't fall and they are mostly controlled.

 

There are a lot of seizure types.  I hope you find the answer to your questions.

 

 

 

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Posted by: sacornelius@msn.com
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Re: [epilepsy] Seizure Types

 

I don't know many websites, but I have complex partials. I usually can tell a few minutes before I get ready to have a seizure. I just have enough time to sit down. I grit my teeth, and try to get up and move, but afterward I go right back to what I was doing. Usually very tired afterward. TC.

Tammy


From: "'Aina & Pat DeLorenzo' aina-pat@cox.net [epilepsy]" <epilepsy@yahoogroups.com>
To: epilepsy@yahoogroups.com
Sent: Friday, March 27, 2015 4:37:34 PM
Subject: RE: [epilepsy] Seizure Types

 

Hi Erin and all, you may find this most helpful. 

 

http://www.epilepsy.com/learn/types-seizures

 

Pat D


From: epilepsy@yahoogroups.com [mailto:epilepsy@yahoogroups.com]
Sent: Friday, March 27, 2015 1:17 PM
To: epilepsy@yahoogroups.com
Subject: [epilepsy] hi erin again

 

 

sorry to write so much.wanted to ask all i know is gran mal seizures.i know there are a bunch of different kind of seizures.Could someone recommend a website or advice what to look out for.


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RE: [epilepsy] my medication

 

I take 900mg/day. I used to take much more but had side effect problems, especially double vision at 1400mg. I was OK at 1200mg. Then it needed to be lowered as my blood counts were still not recovering. I went to 1100mg then 1000mg and I stuck there for some years. I had started to take the meds three times a day in an effort to reduce the double vision, which worked a bit to reduce the worst of it. So at 1000mg I was supplied with 400mg tabs to take morning and night and 200mg to take midday. I then asked if I could reduce to 900mg to try to reduce some of the early morning sedation (part of which was due to Mysoline it has to be said) so to start off with I simply snapped a 200mg tablet for midday. Later I was issued with 100mg Tegretol (ordinary Tegretol) and I just take that at midday with the 400mg Tegretol Prolonged Release morning and night.

 

I have noticed there is Braille on boxes but didn't know this fails to include dose.

 

In recent times, maybe for a year now, I have been issued with the proper UK issue packs of 56 Tegretol Prolonged Release. I think this must be something to do with the pound to euro exchange rate. Maybe it was cheaper to buy in parallel imports back along and relabel and now it isn't!

 

Rob

 

From: epilepsy@yahoogroups.com [mailto:epilepsy@yahoogroups.com]
Sent: 26 March 2015 15:51
To: epilepsy@yahoogroups.com
Subject: RE: [epilepsy] my medication

 

 

Hi Robert

This is interesting as I have to break my tegretol especially the 200 mg tablets as I only need to take 1100 mg a day, the doctor gave me 1200 but I find that too much, it makes me feel ill. The 1100 is sufficient along with my ceppra. You evidently get the same boxes as I get here in France, I just wish they would put in braille the dosage on the box along with the name, they are pretty good here though as most drugs do have braille on them.

Regards

Adrien



.


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Posted by: "Robert" <group@late-effects-radiotherapy.co.uk>
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