The acupuncture or acupoint links on the right side of the page will help you locate points for placing your CieAura Chips. The Chips work more effectively when placed on the correct acupoint on the body!
CieAura Transparent Holographic Chips™ are effectively computer programmed holograms which when applied to a person or animal, reacts with the person or animals’ natural bio-magnetic field surrounding the body, causing minute positive disruptions of the bio-field and causing the body to balance its own energies.
When the CieAura Transparent Holographic Chips™ are applied to specific acupuncture areas, specific results such as the increase in energy, increase in stamina, deeper, more restful sleep, and other assorted reactions occur, depending on the program formula of the Holographic Chip and the related placement.
CieAura Transparent Holographic Chips™ are designed to interact with the bio-magnetic sheath around the physical body in a combination of ways that have been demonstrated for thousands of years to work effectively to heal and improve life. CieAura Holographic Chips have the look of simple decals on the body or clothing and are totally non-invasive and without any chemical component.
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PureRelief Pain Chip is a safe and effective alternative or supplement to current paintreatments. Pain Relief Chips can be used to relieve back pain, pains from sprains, muscle strains, bursitis, tendonitis, arthritis, headaches, migraines & athletic soreness. A months' supply (18 chips) cost approximately $54.95
The PureRelief Pain Chip interacts with the body's energy and draw the pain out by redirecting the energy. This reduces inflammation. The PureRelief Pain Chip can be used for 1-3 days. Replace if pain returns. Some reports say the best result has been when the PureRelief Pin Chip was placed "between the pain and the brain."
For additional information about Pure Relief Pain Chips Click Here
CieAura PureEnergy Chips provide a holistic, healthy alternative to the current energy products by providing instant energy without the added calories. By utilizing acupuncture points, the Transparent Holographic Chips focus the body and increase energy and stamina. A months' supply (18 chips) cost approximately $54.95 PureEnergy Chips are 100% natural and do not flood the body with fatty sugars. Can be used for approximately 3 days, some report up to 5 days use.
For more in depth information on Pure Energy Click Here
CieAura RestQuiet Chips provide a safe, new approach to getting a peaceful night's sleep. For people who do not want to risk the side effects of sleeping pills, but realize they need more sleep as part of a balanced wellness program. Can be used or 2-3 nights. A months' supply (18 chips) cost approximately $54.95For additional information on Rest Quiet Chips Click Here
Introducing 2 new CieAura Chips
Enhances Athletic Performance
Counteracts your cell phone's emissions and fortifies your body's natural resistance to EMF's
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AUTISM / ASPERGER'S
THIS TESTIMONIAL IS LENGTHY, BUT VERY INTERESTING!!!
My son has recently been diagnosed with Asperger's Syndrome. I am wondering if anyone has any ideas for using the chips for this condition.
Currently I attempt to get him to use the rest chips at night and the energy chip during the day. When I can get him to use the energy chip I usually place it at the same location suggested for ADHD, however, this only last for one day in that place as it starts to bother him, on other days I place it bellow the collar bone.
I do notice a difference in him, that is if I can get it on him. Timing seems to be very important, if I don't get the chips on him early enough, he refuses to use them. Sometimes when he has an outburst he will remove the chip, I believe it is out of frustration.
There are times when he will come to me asking for the chips to be placed on him. I always give him a choice as to where he wears it for the day. I find that the stick issue is also a source of frustration for him which makes the day that much harder with him when they fall off.
My mom has Parkinson's disease, she also removes the chips frequently. I have found that if I place the rest chip on the pillow then put the pillow case on it works well for her. So now she rest a lot better than before. I am planning on doing the same for my son.
Thanks for the suggestions. I have been in contact with Dr. Longmire. He suggested that we use 3 energy chips. One on the sternum the other two to be placed on either side of the collar bone. I had been having mild success with using one chip on the sternum.
Although we have only been doing this since Friday. I have to report my findings to all.
Here in Florida it was a gloomy day, threats of T-storms, even a Tornado warning. Days like that are roller coaster rides in our home. Results: we had completely peaceful, calm day. He even got everything done that he needed to for the day. No fighting with siblings. Did not argue with coming in from playing with his friend. He also mentioned that he didn't have his usual headache that he gets during this kind of weather. Slept very well using rest chip. Saturday was an amazing day. He had a mild outburst that lasted under 5 minutes (Usually 45 minutes to hours). Another peaceful day. Today so far he has done very well. He is waking up in a good mood. Has played very quietly until the rest of us got up. The greatest thing is that he is having so much more patience with my mom (I am a caregiver, 24/7, also using chips on her). His frustration level has decreased. (I do remove the energy chips at night, so that I know he will get a good night sleep.)
Now we are nearing the end of day 3. I have to say I am truly amazed. Andrew has had a great day, there have been several things that have occurred during the day today that would have started and outburst or meltdown. (Meltdowns seems to be the term that I am finding with all my research. It is so amazing not to be walking on eggs shells the last few days. If you have a child with Aspergers you know exactly what it is that I mean.
Now I am waiting to see how long a set of 3 chips will last for him.
I will be adding more to this post over the next several day, even weeks. I am hoping that this will be helpful to others that are in our situation.
Day 4 I am amazed with the results I am getting. The day went well. Babysitter had no complaints about behavior when I arrived home from doctors office. Just normal sibling issues. No outbursts, no major frustration. Overall good mood. I can hardly believe that this is the same child. Still an issue getting to bed on time, but more cooperative with that too. My only concern is that he is now showing some signs of redness even with moving them around. I guess I will have to play with that one. As long as he is not bothered by it then we are doing great.
More about day 4
Andrew has now gone 4 full days without any meltdowns. I have to say that I can't believe what is happening for my wonderful son. Yesterday was a very hard day with taking my mom to the doctor and information I got about her condition. Usually Andrew reacts very strongly with my mood. It was so amazing that my mood didn't seem to bother him at all. Several more things occurred yesterday that should have set him off - we were all waiting for it - NOTHING. I like the fact that this is all natural - the only side effect seems to be peace for him and our family. We still have to work on his going to bed on time and to staying in his room. He is sleeping straight through the night without any issues. He has become a happier little boy. Thank God I have found something that helps him. I can now pay more attention to educating him and caring for mom during the day. What a blessing this is for us all.
Andrew has now gone 4 full days without any meltdowns. I have to say that I can't believe what is happening for my wonderful son. Yesterday was a very hard day with taking my mom to the doctor and information I got about her condition. Usually Andrew reacts very strongly with my mood. It was so amazing that my mood didn't seem to bother him at all. Several more things occurred yesterday that should have set him off - we were all waiting for it - NOTHING. I like the fact that this is all natural - the only side effect seems to be peace for him and our family. We still have to work on his going to bed on time and to staying in his room. He is sleeping straight through the night without any issues. He has become a happier little boy. Thank God I have found something that helps him. I can now pay more attention to educating him and caring for mom during the day. What a blessing this is for us all.
Day 5 Today was another gray day, threats of rain. He has been getting up at 6 a.m. to watch a TV show that he likes. I usually get mom up at 7:30. When I looked over at him he had fallen asleep on the couch with all 3 chips on him, 2 at the collar bone and 1 between the shoulder blades (he won't allow tape on his chest). He woke up from this 45 minute nap in a good mood. When I needed help with mom today he came running faster than usual and didn't complain about moving the wheel chair for me.
The lady that watched the kids yesterday stopped by for a short time. She wanted to tell me how amazing it was watching him. She has seen Andrew in action when he is set off. She told me he is like a completely different person. There were a couple times that she thought he was going to go off and he didn't.
This afternoon after his sister got home from school he did pretty well. He got over the fact that he missed his time to play outside with his friend. Andrew and Heidi (sister) where playing for awhile, I have no idea what happened but they starting fighting. He was able to let it go rather quickly. He did not go to his room slamming the door and didn't pull his bed apart. He just took time away from being near his sister. I guess this is a more normal interaction between siblings. (I am an only child - I am lacking in this department.)
When Robert (brother) came home from school with a friend he did very well. The 3 of my kids had a pillow fight. I was on edge waiting for the normal explosion to occur, it didn't.
Bedtime could be going better, but when he finally decides to get into bed under the covers he is falling asleep better. We are slowly trying to change the bedtime routine, all in small steps. It seems that with using the 3 energy chips during the day, taking them off and using the sleep chip has been helping out a lot. It was suggested by a friend to attempt to add a 2nd sleep chip at night. I plan on attempting this tomorrow night. He seems so much more balanced and so much more happier. The rest of the family is slightly on edge because we are all waiting for the next explosion because this is what life has been for several years. I hope and pray that this good behavior change continues for him.
A note to Carl Smith. I will look to get the aloe tomorrow if I can get to the store. I have heard this mentioned before, I guess I didn't remember. Thank you.
The lady that watched the kids yesterday stopped by for a short time. She wanted to tell me how amazing it was watching him. She has seen Andrew in action when he is set off. She told me he is like a completely different person. There were a couple times that she thought he was going to go off and he didn't.
This afternoon after his sister got home from school he did pretty well. He got over the fact that he missed his time to play outside with his friend. Andrew and Heidi (sister) where playing for awhile, I have no idea what happened but they starting fighting. He was able to let it go rather quickly. He did not go to his room slamming the door and didn't pull his bed apart. He just took time away from being near his sister. I guess this is a more normal interaction between siblings. (I am an only child - I am lacking in this department.)
When Robert (brother) came home from school with a friend he did very well. The 3 of my kids had a pillow fight. I was on edge waiting for the normal explosion to occur, it didn't.
Bedtime could be going better, but when he finally decides to get into bed under the covers he is falling asleep better. We are slowly trying to change the bedtime routine, all in small steps. It seems that with using the 3 energy chips during the day, taking them off and using the sleep chip has been helping out a lot. It was suggested by a friend to attempt to add a 2nd sleep chip at night. I plan on attempting this tomorrow night. He seems so much more balanced and so much more happier. The rest of the family is slightly on edge because we are all waiting for the next explosion because this is what life has been for several years. I hope and pray that this good behavior change continues for him.
A note to Carl Smith. I will look to get the aloe tomorrow if I can get to the store. I have heard this mentioned before, I guess I didn't remember. Thank you.
Day 6 Our day started out pretty well. My husband took Andrew out for shoes and it went very well. Andrew hates to shop. He was able to pick out 2 pairs of sneakers and the time was short at the store, which is not normal for him.
I did notice during the day that he wasn't drinking enough Gatorade (will not drink water). I started to notice that the benefits were lessening as the hours went by. Last night we had a major outburst/meltdown. The only difference I noticed at that point was the duration. For a change I was able to redirect him, it did take about 40 minutes to accomplish this.
Overall I am still very impressed with the reactions he is having since he has been using the chips. He has been much happier. Life has been a lot easier.
I'd also like you all to remember we do have the complication of caring for my mom which is stressful on all of us. Especially since things are getting harder with her. She is requiring more care and more time, so I am not sure if more of my focus going to mom has to do with it - I am sure to some point it does, I see it in my other 2 children.
I hope that this journal I have kept this week will help others. I plan on adding more tomorrow. After that I will more than likely be updating this about once a week.
If there are any additional questions, suggestions please send me a PM (Private message) or email. I will do my best to get back to you as quickly as possible.
I did notice during the day that he wasn't drinking enough Gatorade (will not drink water). I started to notice that the benefits were lessening as the hours went by. Last night we had a major outburst/meltdown. The only difference I noticed at that point was the duration. For a change I was able to redirect him, it did take about 40 minutes to accomplish this.
Overall I am still very impressed with the reactions he is having since he has been using the chips. He has been much happier. Life has been a lot easier.
I'd also like you all to remember we do have the complication of caring for my mom which is stressful on all of us. Especially since things are getting harder with her. She is requiring more care and more time, so I am not sure if more of my focus going to mom has to do with it - I am sure to some point it does, I see it in my other 2 children.
I hope that this journal I have kept this week will help others. I plan on adding more tomorrow. After that I will more than likely be updating this about once a week.
If there are any additional questions, suggestions please send me a PM (Private message) or email. I will do my best to get back to you as quickly as possible.
Day 7 Today I wasn't early enough with getting the chips on Andrew. When I finally had the time to get to applying them to him he totally refused them. So of course our day was very difficult to say the least. We had lots of frustration, a couple of meltdowns. He wasn't happy like has been for the last several days. He was only content when he was doing exactly what he wanted to do. He spent a lot of time playing outside with his dad yesterday. He had a friend come over to play and I took notice to the fact that he was getting frustrated with him too.
What I have learned over the last 7 days. Life can be easier for a child that is living with Aspergers. They can be much happier and more willing to cooperate. I have learned that with using the energy chips on a daily basis it helps the rest chip to work even better for him. I have also learned how important it is to really watch his fluid intake and that I must get the chips on him first thing in the morning. I have learned that my life can be easier and that with using the chips I will be able to guide/teach him strategies that he will be able to use for the rest of his life. It has given us hope for a more calm life of not living on eggs shells. I have also learned that people on the outside do notice a difference when he is using the chips and when he is not using the chips.
The 3 energy chips used on a daily basis along with the rest chip at night have made a significant difference in my wonderful 9 year old son. (Well he will be 9 on Feb 24.)
Thanks to everyone who has given my family and I the support we need. Have a blessed day to one and all.
What I have learned over the last 7 days. Life can be easier for a child that is living with Aspergers. They can be much happier and more willing to cooperate. I have learned that with using the energy chips on a daily basis it helps the rest chip to work even better for him. I have also learned how important it is to really watch his fluid intake and that I must get the chips on him first thing in the morning. I have learned that my life can be easier and that with using the chips I will be able to guide/teach him strategies that he will be able to use for the rest of his life. It has given us hope for a more calm life of not living on eggs shells. I have also learned that people on the outside do notice a difference when he is using the chips and when he is not using the chips.
The 3 energy chips used on a daily basis along with the rest chip at night have made a significant difference in my wonderful 9 year old son. (Well he will be 9 on Feb 24.)
Thanks to everyone who has given my family and I the support we need. Have a blessed day to one and all.
WEEK 2: Needless to say it has been a rather interesting experience with Andrew. He had another good week. We did miss using the chips 2 days in a row. The amazing thing was the first day, there were things that should have set him off into one of his meltdowns and nothing happened at all, purely amazing to me. The second day - well he had a major meltdown that lasted 2 hours, I had to sit on the floor with him - with my arms and legs wrapped around him so that he wouldn't go after his sister or brother. We haven't experienced one of these physically intense meltdowns in a couple of years now. (I sure haven't missed them at all.)
My husband has now been using the chips in the same manner as Andrew. He comes home happier and demonstrates less frustration when the kids are around. However, my husband doesn't seem to realize he would get better results if he would use the chips when he is at home too. I guess this is something that I will have to prove to him with the journal that I am keeping.
If you are sharing my story with others. PLEASE make sure that who ever is using the chips understands that they have to be well hydrated, I have been having some trouble with Andrew on this note. My husband has told me that he notices he will get itchy at the location of the chips, finally he figured out that when he feels like this all he needs to do is get a drink of water and the issue is resolved.
Overall, I can't believe how much easier that last two weeks have been on our family. It is so incredible not having to wait on when the next explosion is going to occur. It is not only an adjustment that Andrew is going through, the rest of us have been on edge because we really are not sure what to expect. We are all praying that this continues to work so well.
I'D LIKE TO ASK A FAVOR PLEASE: If you have anyone that starts using the energy chips with individuals that have Aspergers/Autism. Would you have them keep a journal for me and/or contact me via email. I would like to get further documentation on how this is working for people (positive and negative results). I'd like to be able to send all of our results to Dr. Longmire, for his evaluation. Coming from one source would be easier for him to handle. As most of us know he has been published numerous time during his career. This not only would assist with making CieAuara into a household name; just think of the countless individuals who are suffering in a way that we can't even imagine.
My husband has now been using the chips in the same manner as Andrew. He comes home happier and demonstrates less frustration when the kids are around. However, my husband doesn't seem to realize he would get better results if he would use the chips when he is at home too. I guess this is something that I will have to prove to him with the journal that I am keeping.
If you are sharing my story with others. PLEASE make sure that who ever is using the chips understands that they have to be well hydrated, I have been having some trouble with Andrew on this note. My husband has told me that he notices he will get itchy at the location of the chips, finally he figured out that when he feels like this all he needs to do is get a drink of water and the issue is resolved.
Overall, I can't believe how much easier that last two weeks have been on our family. It is so incredible not having to wait on when the next explosion is going to occur. It is not only an adjustment that Andrew is going through, the rest of us have been on edge because we really are not sure what to expect. We are all praying that this continues to work so well.
I'D LIKE TO ASK A FAVOR PLEASE: If you have anyone that starts using the energy chips with individuals that have Aspergers/Autism. Would you have them keep a journal for me and/or contact me via email. I would like to get further documentation on how this is working for people (positive and negative results). I'd like to be able to send all of our results to Dr. Longmire, for his evaluation. Coming from one source would be easier for him to handle. As most of us know he has been published numerous time during his career. This not only would assist with making CieAuara into a household name; just think of the countless individuals who are suffering in a way that we can't even imagine.
Week 3: Andrew's Birthday was on Wednesday. He had such a wonderful day, happy all day long, even with having to wait for his gifts. This week has gone very well for him.
We still need to get a lot of the routines going better in our home.
His meltdowns, attitudes, hurtful words, slamming of doors, horrible reactions when he doesn't get what he wants, no rages when he finds out he finished one of his favorite snacks or meals. He is also demonstrating a lot more patience with having to wait his turn. Less interrupting when others are talking. He is even handling the fact that his daddy is working mostly nights this week (he really hates that.)
His dad on the other hand has not continued with using the chips. He only used them for a week. He did have a positive response when using them. When a person has Aspergers (not sure about HF autism) there can also be additional diagnosis that goes along with this. Such as depression, OCD, etc. I guess that being a diabetic also contributes to the possibility of depression. Last week he was in a better mood, seemed more at peace, better cooperation, something very different on the positive side. This week without chips he is back to a poor mood, no sign of peace, less cooperation, back to being on the negative side.
If there are any questions I am not answering with my log please don't hesitate to contact me or post them here. I will attempt to answer questions if we have had any experience with it.
We still need to get a lot of the routines going better in our home.
His meltdowns, attitudes, hurtful words, slamming of doors, horrible reactions when he doesn't get what he wants, no rages when he finds out he finished one of his favorite snacks or meals. He is also demonstrating a lot more patience with having to wait his turn. Less interrupting when others are talking. He is even handling the fact that his daddy is working mostly nights this week (he really hates that.)
His dad on the other hand has not continued with using the chips. He only used them for a week. He did have a positive response when using them. When a person has Aspergers (not sure about HF autism) there can also be additional diagnosis that goes along with this. Such as depression, OCD, etc. I guess that being a diabetic also contributes to the possibility of depression. Last week he was in a better mood, seemed more at peace, better cooperation, something very different on the positive side. This week without chips he is back to a poor mood, no sign of peace, less cooperation, back to being on the negative side.
If there are any questions I am not answering with my log please don't hesitate to contact me or post them here. I will attempt to answer questions if we have had any experience with it.
SCIATICA
I’m sorry I haven’t been quicker to respond, work this week has been a crazy one. Yes, I have used the chips. I placed one of the chips on the Bladder 54, in the center of the back of the knee crease, and that worked great. I placed the other on my butt where I thought was the source of pain, no relief so I moved it and it helped a lot, especially when I got into my friends car and made it flair up again. By morning I was much better. What I notice most about the chips is when I first put them on I felt like I was buzzing, a lot like a trembling, but in a good way.
Jacque,
Oregon
12/ 19/ 09
There are so many testimonials about people with migraines, and this week my husband Tim proved the pain chips are an incredible help with the migraines he's had all his life. As a Homeopath, Reiki Master, Master Rapid Eye Therapist, Hypnotist, and certified in Emotional Freedom Techniques, I have tried everything to help relieve his migraines, to no avail. UNTIL NOW!!!! Tim woke up with the worst migraine he can ever remember, and after I placed a Pure Relief Pain chip near the painful spot on the back of his neck, the pain reduced within minutes, and he fell fast asleep. He also had good energy in the morning, when he normally is wasted after a headache of that severity!!! Amazing!
12/17/09
Charlotte Garland
Winnsboro, Tx
My husband Tim, is a moaner. He moans most every night during sleep, and has as far as I can remember. I first night I put the Pure Energy and Pure Relief chips on him, his moaning stopped and his snoring has improved a great deal. We had not even used the Rest Quiet Chips yet! This is a welcomed improvement in our 35 years marriage. I am so grateful to have found CieAura!!! His sleep remains improved even after 3 months.
Charlotte Garland
Winnsboro, Texas
November 24, 2009
I have been using three pain chips on my back for the fractured disc and can hardly believe that they actually work just fine. Before using them I was taking a lot of the Dilaudid and sometimes it still didn't help with the numbing sensation on my right knee. The chips help it and I can't believe it. I've also been using the Rest/Quiet chips and have been sleeping better than ever. In fact, if I don't remember to take it off early in the morning, I tend to oversleep past 7 am!
So, thank you for telling me about these chips, they have been a God send.
Best,
John xxxxx
August 05, 2009, 11:05:13 PM
I started using the Pure Energy chips 4 weeks ago. I feel great everyday! I have a B12 deficiency and have to take B12 shots anywhere from every 2-4 weeks just to be able to get out of the bed everyday and have never been able to go longer than 4 weeks between shots. After weeks of feeling great, the other day I started realizing how tired I was feeling. My family and I had just made 2 8-9 hour trips (one way) in 3 weeks, so I chalked it up to that. Well, the next morning I woke up...same thing...dog tired, and that is how it usually hits me when it is time for a shot. I got to thinking about it and couldn't remember when I had gotten my last shot. I looked through my calendar, and was SHOCKED!! It had been 7 WHOLE WEEKS since my last B12 injection! I have NEVER made it that long and felt so great! I also have been using the Rest Quiet chips and love them. I have never been a good sleeper, but my daughter was born 16 months ago and she still gets up every 3-4 hours at night for a bottle (she's tiny and can't hold very much). She has a rare bone disease as well and doesn't sleep soundly. I have only gotten 3-4 hours of sleep a night since she has been born. Since beginning to use the Rest Quiet chips, I am sleeping no more than usual, but wake up feeling rested...after 3-4 hours of non-consecutive sleep!! People have even started telling me how rested I look and immediately assume my daughter is sleeping better!! Needless to say, I think these products are awesome!!
Pure Relief Testimonial
June 21, 2009, 07:58:44 AM
After a rather active life (3 knee surgeries, 2 shoulder surgeries, reconstructed left wrist, a 3-inch long plate in my neck, 3 bulging disks in my lower back, and numerous broken bones) my doctors placed me in long term pain management for chronic pain. This consisted of a combination of 120 mg of Oxycontin, 1050 mg of Soma, 10 mg of Valium, and 2400 mg of Ibuprofen per day. In January of 2009, a friend gave me samples of the Pure Relief pain chips. I looked at what appeared to be pieces of scotch tape with something printed on it and thought how can this possibly do anything, but decided to give them a try. Much to my surprise, the chips worked. Most days I have little or no pain and have not taken any pain medications (other than an occasional ibuprofen) in over four months.
Now is an Independent Sales Rep not only am I making a nice additional income but can buy my pain chips for less than the co-pay was for my medications. I'm just happy I have chips! I rally love them. I haven't taken an Excedrin since I go the chips and there hasn't been a week go by in 5 years that I didn't take them. They worked great on a friend who just had surgery and I put them around his incisions and in 5 minutes he was painless!
Yesterday was my sister Lynn's chemo day. She has Pancreatic Cancer. On the way she got a screaming headache that was turning to a migraine. I happen to have some rest chips with me and placed one just below her temple. The side where the pain was. In a few minutes the headache moved to the otherside of her head and then vanished. She did her treatment and when we got back to the house she commented that she has never felt so relaxed. She had been reluctant to try the chips because of the chemo. I reassured her there would be no chemical exchange and should not interfere. I was so thankful to have the chips available to her because the chemo gives her the shakes inside and the chips calmed it away. What a blessing these chips are.
Mary C.
One of our clients has severe TMJ. The pain is so bad it wakes her up at night and can't go back to sleep. She put one pain chip on her jaw. She slept all night pain free! AND she slept even better cause she had her husband use the sleep chip and his snoring was WAY better... :-) Ruby
I had a serious auto accident 4 years ago. My seat back broke down, I slid out from under my seat belt and the air bag didn't deploy -- AS I WENT OVER AND OVER down a mountainside. The muscles in my upper arms and my thighs had been injured from the seat belt as I slid out from under it. Recently, those muscles have been hurting again. (I think like a Fibromyalgia pain) . . . I put a chip on each arm and each thigh. I found the spots by pressing until I found sore spots. PAIN GONE! Not instantaneous with this, but maybe after several hours. THEN, I had a tooth extracted by an oral surgeon. It had to be cut out in pieces. I tried a pain pill on the way home, but it did little to no good. Before I went to bed, I thought to put a pain chip on my jaw. NO PAIN, NO SWELLING and it healed super fast! I did put another chip on it two days later -- but do not think I will need another one.
I wish I had these years ago!!!!!!!!!!
Georgiana Duncan
New River, AZ
I am so excited! Last week end we worked in Lufkin. Saw many clients. I saw a man by the name of R.J. His wife had recently had a stroke and was in the hospital. She had just that day been put in ICU with pneumonia, kidney infection and blood clots in both legs. He was distraught. His major issue concerning her was that she had given up. She would not work with the therapists. Would not eat. Would not cooperate at all. It was like she had no desire to get well. I texted Blake to ask if he knew of any testimonials with people that were just past having a stroke. He said he did not ... but that it wouldn't hurt to chip em up.
I asked R.J. if he would be willing to put some little stickers on Evelyn. I told him that just possibly it would get her motivated to do something.... and then again it might not make any difference at all. I suggested he start by putting one Energy on the upper chest -- the lung point. I asked him to watch her for any changes. He called the next day and said he couldn't see any difference at all. I suggested he continue putting the Energy chip on but to move it to the solar plexus area.... and to continue to watch for any changes.... and to change it every three days. Well! He just called. He is very excited. She is better in all ways. Kidneys are better, pneumonia is better, blood clots are better ..... now I am certain that is all due to what the doctors are doing ------ although the chips do help the frequency and vibration of the body .... might be a combination of the two. But .... to why I am excited (!!!!!). She is acting differently....... she is eating and cooperating! He is excited! She is getting back to her old feisty self! That had to be the Chips!
Ruby
Tyler Texas
