📄 23 mins.
Story #1

I’ve debated sharing yet, bc I’d hate for our success to be minimized and poo-poo’d. We’ve come through SO much and I know for sure that Joe’s protocol along with Jane’s protocol have been key. Well here it is:
My husband collapsed October 1,2018 and was diagnosed with a large, rare brain tumour . Gross total resection within a few hours because it was fully blocking the flow of cerebral spinal fluid in his brain and he was at risk of sudden death. At 6’ tall, and after 40 days in hospital, he was down to 124 lbs. lost ability to swallow and talk and walk for the first couple weeks. Swallow only returned by about day 30 or so. Guys, it was so awful. But we believed God had good plans for my husband and stood determined to get better.
They said no chemo could help, and radiation was a 50/50 chance of being helpful. There’s no major research to go on bc this tumour was so rare. We opted not to do radiation. My husband was back talking, walking, driving, and working in February. And by March a routine mri found that stupid tumour had fully returned and was about to kill him. The hospital experience had been so full of mistakes and pain for him, he refused surgery and we learned about and started both Joe and Jane’s protocols. Unfortunately the tumour was too big and fully blocked the brain again. Ambulance trip followed by him coding was so scary, and I was told I could let him pass peacefully. I refused. I asked my husband to do it all again for me, for our kids, and for our new baby I was carrying. He did it. Another gross total resection and the mri the day after showed they got 95% of it. Lost swallow etc but regained it and went home to recover after only 20 days.
Here’s where the protocol comes in:
He had no treatment and no mri for two months after surgery because they wanted him to gain weight & strength to prepare for radiation. At the 2 month mark, a pre-radiation mri showed zero growth. No change. Guys, based on the aggressive nature of that tumour the first time, we’d have expected to see at least some growth. But we had hit it HARD with daily fenbendazole and the full Joe protocol, and I’d made a metro map for him and it was clearly working.
During radiation he had no nausea or headaches/brain swelling that they expected, and I’m sure it’s again bc of the meds & supplements from joe and Jane’s protocols.
My husband is home and walking, talking, driving, starting to volunteer at his old job, and able to be part of our family. We get to keep him rather than “letting him pass peacefully” and he’s never stopping the fenbendazole. Thank you JESUS and thank you ****** and ******.
So much heartache the last few years and especially the last one. Shortly after my husband came home the second time, I lost the baby he fought to live for. But today we listened to the heartbeat of a beautiful rainbow baby I’m carrying now. There is hope. So much hope. ♥️

Story #2

……………………

Story #1

I’ve debated sharing yet, bc I’d hate for our success to be minimized and poo-poo’d. We’ve come through SO much and I know for sure that Joe’s protocol along with Jane’s protocol have been key. Well here it is:

My husband collapsed October 1,2018 and was diagnosed with a large, rare brain tumour . Gross total resection within a few hours because it was fully blocking the flow of cerebral spinal fluid in his brain and he was at risk of sudden death. At 6’ tall, and after 40 days in hospital, he was down to 124 lbs. lost ability to swallow and talk and walk for the first couple weeks. Swallow only returned by about day 30 or so. Guys, it was so awful. But we believed God had good plans for my husband and stood determined to get better.

They said no chemo could help, and radiation was a 50/50 chance of being helpful. There’s no major research to go on bc this tumour was so rare. We opted not to do radiation. My husband was back talking, walking, driving, and working in February. And by March a routine mri found that stupid tumour had fully returned and was about to kill him. The hospital experience had been so full of mistakes and pain for him, he refused surgery and we learned about and started both Joe and Jane’s protocols. Unfortunately the tumour was too big and fully blocked the brain again. Ambulance trip followed by him coding was so scary, and I was told I could let him pass peacefully. I refused. I asked my husband to do it all again for me, for our kids, and for our new baby I was carrying. He did it. Another gross total resection and the mri the day after showed they got 95% of it. Lost swallow etc but regained it and went home to recover after only 20 days.
Here’s where the protocol comes in:

He had no treatment and no mri for two months after surgery because they wanted him to gain weight & strength to prepare for radiation. At the 2 month mark, a pre-radiation mri showed zero growth. No change. Guys, based on the aggressive nature of that tumour the first time, we’d have expected to see at least some growth. But we had hit it HARD with daily fenbendazole and the full Joe protocol, and I’d made a metro map for him and it was clearly working.

During radiation he had no nausea or headaches/brain swelling that they expected, and I’m sure it’s again bc of the meds & supplements from joe and Jane’s protocols.

My husband is home and walking, talking, driving, starting to volunteer at his old job, and able to be part of our family. We get to keep him rather than “letting him pass peacefully” and he’s never stopping the fenbendazole. Thank you JESUS and thank you ****** and ******.

So much heartache the last few years and especially the last one. Shortly after my husband came home the second time, I lost the baby he fought to live for. But today we listened to the heartbeat of a beautiful rainbow baby I’m carrying now. There is hope. So much hope. ♥️

Story #2

12/26/19- my husband woke from a nap and was unable to answer questions appropriately….. off to the ER we go. They found a mass in his left upper lobe (lung), a large mass in left side of his brain and several other lesions.

12/28/19 – we were transferred to St Joseph Hospital (Barrow Neurological Center) in Phoenix Az.

12/29/19 – 1/2/2020 – met a multitude of physicians that are all very knowledgeable, caring and skilled at their area of profession.

1/3/2020 – All consents signed, preop complete. He goes in for removal of the brain mass in 2 hours and 9 minutes…. please PRAY!!! 🙏🙏🙏🙏

We started Joe’s protocol Saturday 12/28/2019….
I honestly believe that between GOD, JESUS CHRIST, Joe’s protocol and the amazing team of doctors and healthcare workers….. we will be free if cancer!

Update: 1/3/2020 – I just spoke with the Neuro surgeon….. they removed all of the tumor! No surprises…… GOD IS GOOD!!! Thank you for all of your prayers!! God hears them! 🙏🙏🙏🙏

God bless you all! Prayers to everyone here…. to the ones that are fighting the cancer and the loved ones that are by their sides…..

Story #1

I’ve debated sharing yet, bc I’d hate for our success to be minimized and poo-poo’d. We’ve come through SO much and I know for sure that Joe’s protocol along with Jane’s protocol have been key. Well here it is:
My husband collapsed October 1,2018 and was diagnosed with a large, rare brain tumour . Gross total resection within a few hours because it was fully blocking the flow of cerebral spinal fluid in his brain and he was at risk of sudden death. At 6’ tall, and after 40 days in hospital, he was down to 124 lbs. lost ability to swallow and talk and walk for the first couple weeks. Swallow only returned by about day 30 or so. Guys, it was so awful. But we believed God had good plans for my husband and stood determined to get better.
They said no chemo could help, and radiation was a 50/50 chance of being helpful. There’s no major research to go on bc this tumour was so rare. We opted not to do radiation. My husband was back talking, walking, driving, and working in February. And by March a routine mri found that stupid tumour had fully returned and was about to kill him. The hospital experience had been so full of mistakes and pain for him, he refused surgery and we learned about and started both Joe and Jane’s protocols. Unfortunately the tumour was too big and fully blocked the brain again. Ambulance trip followed by him coding was so scary, and I was told I could let him pass peacefully. I refused. I asked my husband to do it all again for me, for our kids, and for our new baby I was carrying. He did it. Another gross total resection and the mri the day after showed they got 95% of it. Lost swallow etc but regained it and went home to recover after only 20 days.
Here’s where the protocol comes in:
He had no treatment and no mri for two months after surgery because they wanted him to gain weight & strength to prepare for radiation. At the 2 month mark, a pre-radiation mri showed zero growth. No change. Guys, based on the aggressive nature of that tumour the first time, we’d have expected to see at least some growth. But we had hit it HARD with daily fenbendazole and the full Joe protocol, and I’d made a metro map for him and it was clearly working.
During radiation he had no nausea or headaches/brain swelling that they expected, and I’m sure it’s again bc of the meds & supplements from joe and Jane’s protocols.
My husband is home and walking, talking, driving, starting to volunteer at his old job, and able to be part of our family. We get to keep him rather than “letting him pass peacefully” and he’s never stopping the fenbendazole. Thank you JESUS and thank you ****** and ******.
So much heartache the last few years and especially the last one. Shortly after my husband came home the second time, I lost the baby he fought to live for. But today we listened to the heartbeat of a beautiful rainbow baby I’m carrying now. There is hope. So much hope. ♥️

Story #2

……………………

Story #1

I’ve debated sharing yet, bc I’d hate for our success to be minimized and poo-poo’d. We’ve come through SO much and I know for sure that Joe’s protocol along with Jane’s protocol have been key. Well here it is:

My husband collapsed October 1,2018 and was diagnosed with a large, rare brain tumour . Gross total resection within a few hours because it was fully blocking the flow of cerebral spinal fluid in his brain and he was at risk of sudden death. At 6’ tall, and after 40 days in hospital, he was down to 124 lbs. lost ability to swallow and talk and walk for the first couple weeks. Swallow only returned by about day 30 or so. Guys, it was so awful. But we believed God had good plans for my husband and stood determined to get better.

They said no chemo could help, and radiation was a 50/50 chance of being helpful. There’s no major research to go on bc this tumour was so rare. We opted not to do radiation. My husband was back talking, walking, driving, and working in February. And by March a routine mri found that stupid tumour had fully returned and was about to kill him. The hospital experience had been so full of mistakes and pain for him, he refused surgery and we learned about and started both Joe and Jane’s protocols. Unfortunately the tumour was too big and fully blocked the brain again. Ambulance trip followed by him coding was so scary, and I was told I could let him pass peacefully. I refused. I asked my husband to do it all again for me, for our kids, and for our new baby I was carrying. He did it. Another gross total resection and the mri the day after showed they got 95% of it. Lost swallow etc but regained it and went home to recover after only 20 days.
Here’s where the protocol comes in:

He had no treatment and no mri for two months after surgery because they wanted him to gain weight & strength to prepare for radiation. At the 2 month mark, a pre-radiation mri showed zero growth. No change. Guys, based on the aggressive nature of that tumour the first time, we’d have expected to see at least some growth. But we had hit it HARD with daily fenbendazole and the full Joe protocol, and I’d made a metro map for him and it was clearly working.

During radiation he had no nausea or headaches/brain swelling that they expected, and I’m sure it’s again bc of the meds & supplements from joe and Jane’s protocols.

My husband is home and walking, talking, driving, starting to volunteer at his old job, and able to be part of our family. We get to keep him rather than “letting him pass peacefully” and he’s never stopping the fenbendazole. Thank you JESUS and thank you ****** and ******.

So much heartache the last few years and especially the last one. Shortly after my husband came home the second time, I lost the baby he fought to live for. But today we listened to the heartbeat of a beautiful rainbow baby I’m carrying now. There is hope. So much hope. ♥️

Story #2

12/26/19- my husband woke from a nap and was unable to answer questions appropriately….. off to the ER we go. They found a mass in his left upper lobe (lung), a large mass in left side of his brain and several other lesions.

12/28/19 – we were transferred to St Joseph Hospital (Barrow Neurological Center) in Phoenix Az.

12/29/19 – 1/2/2020 – met a multitude of physicians that are all very knowledgeable, caring and skilled at their area of profession.

1/3/2020 – All consents signed, preop complete. He goes in for removal of the brain mass in 2 hours and 9 minutes…. please PRAY!!! 🙏🙏🙏🙏

We started Joe’s protocol Saturday 12/28/2019….
I honestly believe that between GOD, JESUS CHRIST, Joe’s protocol and the amazing team of doctors and healthcare workers….. we will be free if cancer!

Update: 1/3/2020 – I just spoke with the Neuro surgeon….. they removed all of the tumor! No surprises…… GOD IS GOOD!!! Thank you for all of your prayers!! God hears them! 🙏🙏🙏🙏

God bless you all! Prayers to everyone here…. to the ones that are fighting the cancer and the loved ones that are by their sides…..

Story #1

I’ve debated sharing yet, bc I’d hate for our success to be minimized and poo-poo’d. We’ve come through SO much and I know for sure that Joe’s protocol along with Jane’s protocol have been key. Well here it is:
My husband collapsed October 1,2018 and was diagnosed with a large, rare brain tumour . Gross total resection within a few hours because it was fully blocking the flow of cerebral spinal fluid in his brain and he was at risk of sudden death. At 6’ tall, and after 40 days in hospital, he was down to 124 lbs. lost ability to swallow and talk and walk for the first couple weeks. Swallow only returned by about day 30 or so. Guys, it was so awful. But we believed God had good plans for my husband and stood determined to get better.
They said no chemo could help, and radiation was a 50/50 chance of being helpful. There’s no major research to go on bc this tumour was so rare. We opted not to do radiation. My husband was back talking, walking, driving, and working in February. And by March a routine mri found that stupid tumour had fully returned and was about to kill him. The hospital experience had been so full of mistakes and pain for him, he refused surgery and we learned about and started both Joe and Jane’s protocols. Unfortunately the tumour was too big and fully blocked the brain again. Ambulance trip followed by him coding was so scary, and I was told I could let him pass peacefully. I refused. I asked my husband to do it all again for me, for our kids, and for our new baby I was carrying. He did it. Another gross total resection and the mri the day after showed they got 95% of it. Lost swallow etc but regained it and went home to recover after only 20 days.
Here’s where the protocol comes in:
He had no treatment and no mri for two months after surgery because they wanted him to gain weight & strength to prepare for radiation. At the 2 month mark, a pre-radiation mri showed zero growth. No change. Guys, based on the aggressive nature of that tumour the first time, we’d have expected to see at least some growth. But we had hit it HARD with daily fenbendazole and the full Joe protocol, and I’d made a metro map for him and it was clearly working.
During radiation he had no nausea or headaches/brain swelling that they expected, and I’m sure it’s again bc of the meds & supplements from joe and Jane’s protocols.
My husband is home and walking, talking, driving, starting to volunteer at his old job, and able to be part of our family. We get to keep him rather than “letting him pass peacefully” and he’s never stopping the fenbendazole. Thank you JESUS and thank you ****** and ******.
So much heartache the last few years and especially the last one. Shortly after my husband came home the second time, I lost the baby he fought to live for. But today we listened to the heartbeat of a beautiful rainbow baby I’m carrying now. There is hope. So much hope. ♥️

Story #2

……………………

Story #1

I’ve debated sharing yet, bc I’d hate for our success to be minimized and poo-poo’d. We’ve come through SO much and I know for sure that Joe’s protocol along with Jane’s protocol have been key. Well here it is:

My husband collapsed October 1,2018 and was diagnosed with a large, rare brain tumour . Gross total resection within a few hours because it was fully blocking the flow of cerebral spinal fluid in his brain and he was at risk of sudden death. At 6’ tall, and after 40 days in hospital, he was down to 124 lbs. lost ability to swallow and talk and walk for the first couple weeks. Swallow only returned by about day 30 or so. Guys, it was so awful. But we believed God had good plans for my husband and stood determined to get better.

They said no chemo could help, and radiation was a 50/50 chance of being helpful. There’s no major research to go on bc this tumour was so rare. We opted not to do radiation. My husband was back talking, walking, driving, and working in February. And by March a routine mri found that stupid tumour had fully returned and was about to kill him. The hospital experience had been so full of mistakes and pain for him, he refused surgery and we learned about and started both Joe and Jane’s protocols. Unfortunately the tumour was too big and fully blocked the brain again. Ambulance trip followed by him coding was so scary, and I was told I could let him pass peacefully. I refused. I asked my husband to do it all again for me, for our kids, and for our new baby I was carrying. He did it. Another gross total resection and the mri the day after showed they got 95% of it. Lost swallow etc but regained it and went home to recover after only 20 days.
Here’s where the protocol comes in:

He had no treatment and no mri for two months after surgery because they wanted him to gain weight & strength to prepare for radiation. At the 2 month mark, a pre-radiation mri showed zero growth. No change. Guys, based on the aggressive nature of that tumour the first time, we’d have expected to see at least some growth. But we had hit it HARD with daily fenbendazole and the full Joe protocol, and I’d made a metro map for him and it was clearly working.

During radiation he had no nausea or headaches/brain swelling that they expected, and I’m sure it’s again bc of the meds & supplements from joe and Jane’s protocols.

My husband is home and walking, talking, driving, starting to volunteer at his old job, and able to be part of our family. We get to keep him rather than “letting him pass peacefully” and he’s never stopping the fenbendazole. Thank you JESUS and thank you ****** and ******.

So much heartache the last few years and especially the last one. Shortly after my husband came home the second time, I lost the baby he fought to live for. But today we listened to the heartbeat of a beautiful rainbow baby I’m carrying now. There is hope. So much hope. ♥️

Story #2

12/26/19- my husband woke from a nap and was unable to answer questions appropriately….. off to the ER we go. They found a mass in his left upper lobe (lung), a large mass in left side of his brain and several other lesions.

12/28/19 – we were transferred to St Joseph Hospital (Barrow Neurological Center) in Phoenix Az.

12/29/19 – 1/2/2020 – met a multitude of physicians that are all very knowledgeable, caring and skilled at their area of profession.

1/3/2020 – All consents signed, preop complete. He goes in for removal of the brain mass in 2 hours and 9 minutes…. please PRAY!!! 🙏🙏🙏🙏

We started Joe’s protocol Saturday 12/28/2019….
I honestly believe that between GOD, JESUS CHRIST, Joe’s protocol and the amazing team of doctors and healthcare workers….. we will be free if cancer!

Update: 1/3/2020 – I just spoke with the Neuro surgeon….. they removed all of the tumor! No surprises…… GOD IS GOOD!!! Thank you for all of your prayers!! God hears them! 🙏🙏🙏🙏

God bless you all! Prayers to everyone here…. to the ones that are fighting the cancer and the loved ones that are by their sides…..

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