Update from NC - Feeling Hopeful

Hello from beautiful North Carolina!

This has been a week of hope. My husband officially started treatments this week. I looked at a pic of him from the week before we got down here & looked at him today. The difference is between night & day. He is looking better already. My husband & I were just shocked at how he looked. His PCP & our local hospital said he had long haul Covid & to just rest & he would get over it. I'm so thankful that we went to another hospital & got the answer to what was REALLY wrong.

A typical day at the clinic starts like this - he weighs in to see where his weight is at. Currently he is about 20 lbs underweight, at one point he was 25 lbs under weight. He doesn't have 25 lbs to spare. He then goes around the corner to see in a chair. He had a PICC line put in on Wednesday. This allows medical personnel to access a vein anytime. Every Monday they draw labs to see where he is on his numbers. Three days a week they draw blood & treat with ozone. This puts oxygen into the blood. It will pass thru the rest of his blood & make it more healthy than what it is now. I'm already seeing a color improvement from what it was when they started last week. They then start one of many daily IV's that he will receive that particular day. He might get minerals, an immune booster, Vit C, glutathione or other blood boosters. They are unable to chelate him at this time because his iron count is not high enough. Chelation really takes a toll on the body & he just isn't ready for that.

From there, he heads to the hyperbaric oxygen chamber room. He removes his shoes & his belt. They then put a special hood on him to concentrate the oxygen flow. It looks something like the hood you see here. He needs to wear ear plugs as well to protect his ear drums.

This is his least favorite therapy. He is under pressure for 45 minutes & then it takes 15 to depressurize the chamber so they can open the door & he can come out. They tried to take him to a deeper depth & but he had a hard time breathing. So, they are keeping him at a moderate depth for now. With the cancer in the lungs & his lungs filling with fluid constantly, he has a hard time breathing sometimes.

Cancer can't survive in an oxygen rich environment. The hyperbaric chamber is very effective at getting oxygen into areas where it previously wasn't oxygen rich. A great way to give cancer its walking papers.

From there he goes to the lymphstar room. This therapy involves putting probes on various parts of his body to activate & drain the lymphatic system. They start with putting the probes on the center of this chest for 6 minutes, then to the back of his neck. Then on either side of the chest under the arms, then sometimes behind the small of his back, pelvic area & behind the knees. Each area is for 6 minutes. Once he is done with probes, he stands on a table that vibrates back & forth. The speed goes from slow to quickly. There are three different levels with level 3 being the most intense. His first day he sat for the first four minutes as he didn't feel he wasn't ready to stand so he sat down for the first 4 minutes. He then stood up & stood on the machine for the last six minutes. This drains the lymphatic system even more. There is more evidence of this later on.

From there he goes to the Rasha room. In this room, he puts headphones on & listens to sounds & music thru a crystal. The headphones need to put on a certain way. I don't know why this needs to be except for maybe certain sounds need to reach certain sides of the brain. This room last about 2 hours. He usually snoozes during this time but I'm sure the healing affects of the sounds are still healing. You can read about the Rasha machine at this link.

At this point, he either goes to the IV suite to finish up for the day or he might head to another room to do a aqua detox foot bath. He did one on Monday & we were totally surprised by what we saw. The water turned black & foamy. The foam indicates toxins draining from the lymphatic system thru his feet. The feet have the biggest pores so this makes total sense.

On Tuesdays & Thursdays he meets with Dr. Sara. At these sessions, she works on the psychological aspects of the healing. He was asked to talk about certain blood members of his family for 10-15 seconds each. His parents, his grandparents on both sides & his spouse or anyone else who had a significant impact on his life. A machine measures the intonation of a persons voice & any emotional response. It then develops a song to help you move thru any emotional issues you have with a certain person. He was able to move thru 2 people this week. When the machine says you are clear of a person, it plays a certain kind of song for you. This kind of therapy is called Evox. You can read about Evox at this link. Psychological healing can hold a person back from the physical healing that needs to take place.

One day a week he meets with Dr. Jane Garcia. She is in her mid 70s but is smart as a whip. She has also had lung cancer that was cured by the methods used in this clinic. We are very grateful to have her & it gives us hope that we are going to beat this. She asked him many questions about his health prior to the diagnosis, how we found out & she was very surprised that he had no symptoms prior to this indicating he had cancer in a very advanced stage. She adjusted the supplements he is supposed to take daily, added a couple of new ones & continued to work on the game plan on getting him on the road to recovery.

One day a week he gets an Aarsota injection. This is developed from his urine that he collected over a period of a few days to equal about 3 liters. It was sent overnight by Federal Express to a company in southern California to develop a injection. The urine has the specific cancer markers for his type of cancer. When this is injected into his body, it goes after the cancer. The stronger the reaction to the injection the better it is. This first go round he had chills, a fever that vascillated between 100.1 & 100.9, really sleepy & of course a sore butt where they shot it into him. As each week goes on, the shot will get stronger. Week 4 will be the strongest & the reaction may be bad. They require that someone go home with the patient & stay the night with them. This way reactions can be monitored & recorded. You can read about the Aarsota injection at this link. Another cancer patient talks about getting Aarsota injections to kick the cancer out of his body.

A few times a week, he gets Ondamed therapy. This therapy involves putting a collar around his neck that is attached to the machine & then a band around his midsection. It uses sound waves to heal the body. The first few days, they used the machine to find out what was wrong with his body exactly, wrote down the numbers & then use those numbers to tune the machine to work on that part of the body. The first thing that came up was that his lymphatic system is out of wack, followed by his lungs, digestive issues & an issue he never told anyone about....not even me. It showed he had a partially detached retina. This healed itself years ago. You can read about Ondamed therapy here.

After the first day of treatments, we came back to the room & he slept for almost 3 hours. The second day, he came back & laid in bed for a couple of hours & we just talked while he recuped. The third day is when he get the Aarsota injection. We came back to our hotel & he got in the tub for awhile. He was chilled & achy. He also slept sitting up in the tub. I gave him a bath while he sat in the tub & then he went & lied down for awhile. Thursday & Friday he actually felt pretty good when we got back. He was smiling & starting to act like him oldself. (More hope!)

He got a couple of pieces of equipment this week to help him. He got a rollator, which is a walker with wheels & a seat. He isn't having difficult walking but since the cancer is in his pelvis, it takes some of the strain off his hips joints. He also got a pillow to get his feet up when he is sleeping. When he is getting a lot of liquids during the day, his feet swell up. I got him some compression stockings as well.

I told him when we came down here that this was all about him. To get him well & to kick cancer out of our lives. Well, life had a different path for us. Many of you know I've had vertigo for almost 12 years. I had been symptom free for about a year. Last week, the vertigo returned with a vengeance. I can't lie down or get up without the world spinning. My two triggers are lack of sleep & stress. Guess what I have an overbundance of right now? (you guessed it) I've had tinnitus for the same length of time I've had vertigo. Back in December, it disappeared for a week. To hear nothing was a huge blessing but it returned later with a vengeance. I'd like you to turn on your TV, go ahead, I'll wait. Now turn the volume level up to 40, that is how loud a TV needs to be in order to cover up my tinnitus. So, my husband talked me into becoming a patient & getting some chelation therapy to maybe rid my body of heavy metals that may be causing the tinnitus. I have titanium pins in my right foot from a surgery that was supposed to make it easier for me to be on my feet longer.....it didn't. I also played in lead gas when I was a kid, helping my grandfather wash lawn mower parts with it & cooling my arms & feet off with it on a hot summers day. I know, so dumb by todays standards, but we didn't know back then. The paperwork is filled out & now I'm just waiting to talk to one of the Dr's to get started.

A few of the staff members said it's common that once you start treating one family member in their clinic, that the accompanying family member also gets some sort of treatment. That wasn't my plan but he insisted & told several staff members to get me the paperwork. I could get Vit. C, nutritional & some other simple stuff without becoming a patient "patient" but to get chelation, they need to check my blood to make sure I'm strong enough to do it. One nurse thought I was afraid of getting poked by the needle for an IV, I said no. I used to donate blood & I've been thru labor & delivery twice, fear of needles & IV's is not an option.

That will close this out for this week. I'll be posting an update next week on how things went. We want to show people that there are options. That chemo & radiation are not always the answer for cancer.

Until next time,

Lori

Update from North Carolina

Greetings from beautiful North Carolina,

It's been an emotional & stressful couple of weeks. Tom had to have drains put in both of his lungs so that we could drain the fluid from his lungs when they needed to be drained instead of going to the hospital & dealing with ER doctors who didn't believe us when we said what needed to be done. It was always the same story, blood work, chest xray to see if that "really" needed to be done. He's had 2 over night stays & many hours waiting in the ER & in the imaging waiting room. You know you've spent to many hours in the waiting room when the staff knows who you are with even tho you didn't come into the room with them.

To see the drain system we are working with here at the hotel. Here is a link to a video showing how it works. Its very emotional on me to see those plastic tubes coming out of his chest on either side. The first time I saw them the saying......We are the borg, you will be assimilated came to mind. (You know I'm a trekkie) But in all seriousness, it's good that we can do this. Bandaging him back up afterwords is a bit of a trick with the special tape but I'm slowly getting the hang of it. We bought some surgical dressing bandages from Walgreens just in case we need them. We are hoping by the end of next month the drains won't be needed.

The first time he had his left lung drained was the day after he was diagnosed with Stage 4 metastatic cancer. They took 2 liters off this lung. Next time you go to a grocery store, take a look at a 2 liter bottle of soda. Imagine that much fluid sitting on one side of your chest area. There isn't that much room! We are averaging 1.1 liters drained off the left lung every 3-4 days & 1.2 liters off the right lung every 2-3 days.

His red blood count & his iron levels are low. We've already told the clinic that if he needs blood, we aren't taking it from the general population. Too many people have donated that are vaccinated & we don't want spike proteins floating around in his body & replicating. We both have the same blood type, so he will take mine. Funny thing about him & I, we both have the same blood type, we both have the same back deformity & we both have an allergy to Cephalexin, although the reaction is different. We need to get his iron count up higher so that they can chelate out any heavy metals that have contributed to this. Currently, they are saying he isn't strong enough to chelate.

He officially starts treatment on Monday. He'll be getting hyperbaric oxygen chamber treatment, food grade peroxide, ozone treatment to his blood, Vit. C & glutathione IV's. Also a Palt treatment which is supposed to prevent uncontrolled cellular proliferation. Basically, reverse the spread of metastatic cancer. Cancer can't survive in an oxygen rich environment. We are making the cancer very unhappy right now. It's probably wondering what happened to its happy home of 20 plus years. We have given it it's walking papers.

We'll be out in the Huntersville/Mooresville, NC area at least thru the end of March. Then we get to go home for 4 weeks. Then we come back out for another 4 weeks of treatments. We were given new hope yesterday. One of the doctors who works at the clinic had lung cancer. She went thru 3 rounds of treatments at Dr. Buttar's clinic. She was cured of the cancer. We'll be spending our wedding anniversary out here. Hopefully, he'll up to a few hours out in public then. Right now, all he has the strength for is to leave our hotel room, go to the clinic & back to the hotel room again.

We did have a pleasant surprise during his second stay. One of his nurses (who shall remain nameless to protect her) is completely anti-vax. She had no clue about Dr. Buttar. We spent a lot of time talking & comparing notes. I gave her Dr. Buttar's website info & his phone number. I also gave her the link for this blog. I hope you are reading this blog entry, a big shout out to you. Thank you for the great nursing care that you did for my husband. I hope we can touch base again in about 6 months when we have this thing beat. My husbands story of how we just round out less than a month ago about this has made the rounds at the hospital. People who I don't know who they are come up & ask how he is doing.

We established a primary physician out here for him. She was more than willing to take him on, willing to make procedure appointments if needed & prescribe pain meds as needed. The ones that Tom's oncologist prescribed back in Ames wasn't strong enough in her eyes. So she prescribed him something a bit stronger. It takes awhile to kick in but does work. We go back to her the last Friday of March for a follow up. Dr. Buttar's office doesn't prescribe pain meds, they prefer that they use alternative forms of pain meds like CBD oil or Arnica. Those work to a point but sometimes something a bit stronger is needed.

This is by far the hardest thing that I've ever had to go thru. All the B.S. I went thru as a kid & the stress of 3 year ago is nothing in comparison to this. Watching a loved one fight cancer that has spread from his prostate to his liver, both lungs, spine & pelvis is heart breaking. He has dropped 25 lbs. He looks like a holocaust survivor. He doesn't have 25 lbs. to lose. We've both have shed many tears together. I shed tears in the shower nightly. Please keep our family in your prayers, this battle is only in the beginning stages & we are determined to win with God's help. All healing comes from him, Dr Buttar & his team are only the tools to make it happen.

Until next time,

Lori

Hello from North Carolina!

Greetings from beautiful North Carolina,

We have temporarily moved from Central Iowa to Charlotte, NC. We left home early on the morning of Feb. 5th & after 2 days of travel, we arrived in the Charlotte area.

My husband had a phone consultation with Dr. Sara on the 7th. She basically explained the program, how things will work. We went in the next day, they drew lots of blood for their lab work & then did an EKG. We went back to the office 2 days later. My husband had his physical exam & they gave him an IV of blood support to try to get his iron level up. The iron level needs to be higher than 10 so they can chelate him to get the heavy metals out. They also gave us this huge box of supplements. (more about this further down)

This program is very vigorous. Once treatment starts, we'll be at the clinic 36 hours a week for 4 weeks. They'll be doing IV therapy, hyperbaric oxygen therapy (cancer can't survive in an oxygen rich environment), hyrdrogen peroxide therapy & specialized shots he'll be getting in his back side every Wednesday.

Right now, he has 31 different types of supplements he has to take at specific times of the day & X amount of each one. The whole daily regimen fits on a 11x17 piece of paper. I mark down what time he took what so we keep track of everything. This is a full time job in & of itself.

He has a lifestyle he has to follow the rest of his life. No sugar (honey, stevia & agave nectar are ok), no alcohol, no pork (he hasn't eaten pork in over 40 years) & no grudges. He also needs to eat Non-gmo foods. This is harder than you think when you go to buy groceries. Dr. Buttar said you'll always have cancer. You need to live your life like you always have cancer otherwise if you fall back to your old lifestyle, it will come back. We all have cancer cells in our body. It's just a matter of them activating & they become hidden from our immune system so they grow. Just like a baby in it's mothers womb. It's hidden from the immune system so that the mom's immune system doesn't reject it & miscarry. (Yes, I know it happens.)

We are in the Charlotte area until the end of March. Then we go home for a month & then come back to Charlotte for another month. Since he is Stage 4, he'll need at least 2 rounds to knock out the cancer.

Until next time,

Lori

New Email address for this blog

Hey Everyone,

First off, let me thank you for your prayers. We hope to be heading to NC soon. He was in the ER & oncology ward again this past weekend with a lot of fluid on the left lung. They drained off 1.5 liters. They left a bit hoping it won't fill up so quickly this time.

Here is the new email for this blog. For some reason, I forgot to log in for over 30 days on the last one & lost use of the email address.

vaccinefreehealth@gmail.com

Until next time,

Lori

Devastating News

Hello to all of my readers,

Last week I wrote about how Covid & the Covid vaccine has affected my family.

I took my husband into the ER in Ames on Sunday. He was very pale, breathing rapidly & was very weak. Within about 15-20 minutes of him being in the isolation/exam room the ER physician ordered a CT scan from head to pelvis. We were not prepared for the news we were about to hear.

The ER physician said there is no easy way to tell you this. You have metastatic cancer of the prostate, liver, lungs, spine & maybe the hip area. His oncologist is pushing for chemotherapy. This might buy us a few years at best.

But what about quality? The quality of life just won't be there. He saw his sister go thru chemo & radiation when she had brain cancer when she was 19 & again when she was 55. We just aren't going to go that route.

We've decided we are going to tackle this naturally. We've ordered the NAD protocol to start with. We are then going to travel to NC to Dr. Rashid Buttar for further natural treatment.

We are determined to beat this. Please keep our family in your prayers. I know I have a few prayer warriors out there. I will update as they become available. We should have the biopsy results tomorrow.

Until next time,

Lori

How has Covid affected you?

Greetings from Iowa,

As Covid & the various varients circle the globe, the news headlines say fear, fear, fear. I've NEVER feared this virus this entire time, not even when I got sick with it 15 months ago. YHVH tells us 365 times in the bible to Fear not. I think that is pretty strong message to not fear.

I had Covid 15 months ago. It was a bad respiratory illness. (I've had worse) When I had a fever, my joints felt like they were in a vice & someone was trying to tighten the vice down continually. That first night I was screaming because the pain was so bad. I finally gave in about 3 am the next morning to ease the pain & so I could get some sleep.

I ordered some D3 & mega dosed for 2 weeks, I had it beat in 5 days. 150,000 IU daily for 2 weeks. I have a lingering cough that has been slowly going away since then.

My husband always said he was bullet proof & that this virus wasn't going to take him down. Well, he should have been move careful about what he said. Towards the end of April of 2021, he started to come down sick. He continued to work. At our wedding in May, he was really sick but was bound determined that we were not going to change our wedding date. We got married on May 16, 2021. Three days later he went to our local clinic to get checked out. He tested positive for Covid & he also had double pneumonia. Nine plus months later he is still fighting the pneumonia. He has lost 15 lbs. (he didn't have 15 to lose) He is very anemic. We tried the allopathic method & it wasn't getting us anywhere. He is neubulizing Collodial Silver now & we have Copper hydrosol coming so he can neubulize that as well.

How many of you have been affected by the vaccine? Whether personally or thru a family memmber? I'm sad to say that 7 family members have been negatively affected by the vaccine. We tried to educate them about the dangers but ultimately they decided the benefit outweighed the risk.

Three family memebers have been injured by the vaccine. One injury was a blood clot that developed in his leg & the doctors thought they were going to have to amputate his leg. Fortunately it didn't happen......but he still promotes others to get it. I don't get it. The other 2 members haven't put the pieces together.

I have four family members that have been adversely affected by the vaccine. One got sick from all 3 shots, the 3rd one really got them & now they have tested positive for Covid. One family member got sick after the 2nd & 3rd one. Two got sick after the 3rd one.

Our church has written about 560 religious exemption letters & only one has been rejected so far. They have gone all over the US, Canada & six went down to Australia. (It took 4 weeks to get there)

If your employer is saying employees have to get the shot or lose their job. Get a group of you together & stand together. More than likely the employer will stand down. This has been happening with many companies around the US.

Stand strong. Fauci's narrative is slowly falling apart. I highly recommend you ready Robert Kenney Jr's book - The Real Anthony Fauci. Fauci is drunk on power. It's time to give him a major reality check & tell him no more. This pandemic is over when people say no to more testing. Say no to vaccines & no to mask mandates. It's time to say enough is enough.

Until next time,

Lori

A Miracle happened tonight

Greetings from a wild & crazy Iowa,

Many of you know about the tornadoes that hit Kentucky & other states. Iowa, Minnesota, Missouri & Illinois are getting hit tonight.

Among the chaos of these storms, a miracle occurred. And I'm so glad it did.

I've been hobbling around our house with a surgical boot the last couple of days. I have a dancers break of my right pinkie toe. Technically, I should be having surgery to put pins in to stabilize it. We don't have insurance, so we are going the boot route for the next 8 weeks hoping the bone will mend without help. p I can walk 5 mph, having to walk at a pace of less than 1 mph is beyond frustrating.

Anyway, the miracle that occurred tonight happened out of the blue. I was upstairs in our bedroom folding clothes. All of the sudden I hear nothing. Now I know what you are thinking, why would this be a surprise? I've had tinnitus in both ears......very loud tinnutis. If the TV volume was on level 30, I could hear the tinnutis above that. It followed me into my sleep even with the fan blowing for white noise.

It's pure heaven to hear silence. To hear......nothing.......is beautiful. 11 years.......8 months.......16 days of constant ringing is gone.

My tinnitus was the last one. Imagine hearing every 24/7/365.

Now I don't hear anything.

I am working on an article about Covid. The genocide is growing daily & the media & the public is ignoring it daily.

Until next time,

Lori