Friday, March 20, 2020
Quarantine 🤦🏼♀️
It has been almost three weeks since I have had my exosome stem cell infusion. It has been a tough three weeks. I have been tired and emotional which is something to be expected. I can't say that I am walking amazing or there has been some life-altering change, but I can say that I feel more "alert." I am very happy that I got two immune-boosting treatments before the virus scare (exosomes and IVIG). This week I am going to be able to start doing more of my regular strenuous exercises. I am very thankful that I do not go to a gym and I see my trainer because I can keep working out for as long as my dad still is letting me go out with the coronavirus. I had to stop my hyperbaric treatments because of the circumstances, but they will start again as soon as the world goes back to normal. I don't want to say that this treatment didn't work because I definitely feel better than I did before I started, but I can't say that I am walking how I want to. This doesn't mean that I will stop trying treatments or doing what doctors say but I'd be lying if I said that I'm not disappointed. This has been a good time for me to slow down and let my body rest, to use exercise equipment at home and appreciate the little things. I have learned a lot from this experience and am going to try to fasting for a week at least once a month, it is a really good way to reset your body and mind. Hopefully, I keep seeing small improvements even if they are as simple as mental clarity.
Saturday, February 29, 2020
Infusion Day 💉😆
Today I got exosomes (stem cells). It didn't take very long and afterward, I got to go on the beemer three times so that the stem cells would move throughout my body. Before and during the treatment I had my feet on a device called a Sima. I also had infrared lights on my head, down my spine, and back of my neck. I looked crazy but we did everything to wake my body up and have the stem cells go to the places that need healing. The red lights are supposed to stimulate and strengthen the mitochondria of the cells and the sima does something with frequencies in your body. When the infusion was done they put me on the Bemer for three rounds because it increases the blood flow of the body. I will continue my fast for the next couple of days and hopefully will see a change. Out of all the videos we have watched and testimonies we have heard, it can take anywhere from immediately, to 3-6 weeks and months for even more differences. At this point, any slight difference would make this all worth it. I am going to take it easy after infusion day and then start moving a lot and get the stem cells flowing so that they can do their job. I hope that you enjoy these crazy pictures of me at 7 am this morning (Not posting the hideous pictures of me with red lights wrapped around my head)
(This is the Sima)
Friday, February 28, 2020
The Day Before! 🥳
Tomorrow is the day! I get my stem cells! I’m going to the doctor early in the morning to get the infusion, and will have to continue the fasting diet for at least two days after (probably will do more). I can slowly resume my regular diet with juices, soups, and soft foods and am aloud to do activity that isn’t to strenuous. The stem cell IV is supposed go pretty quick, maybe 25 min. I’m believing there will be promising results, and am excited to see what happens. After the infusion I get put on something called a bemer, which increases circulation and more. I am so grateful for this opportunity and everyone who has been praying for me, routing for me, and following my story. I’m praying for some change and believe that it has already started.
I will continue to update how I am doing and feeling after the infusion. And how the process goes tomorrow! The following week I will continue to do the hyperbaric oxygen therapy to help my body, and take it easy.
Tuesday, February 25, 2020
Fasting 🚫🍷🍩☕️🚫
As I continue the protocol for my treatment the next step over the next five days is fasting. The program includes a five day fast mimicking package of five days called ProLon. Each box for the day includes packages of "meals" that you eat throughout the day. It is mostly soups and a couple of nut-based bars, teas, and crackers to go with the soup. Each day you follow the instructions and it slowly cuts things out of the diet from the first day or adds in a supplement. You are not allowed to drink caffeine on the diet so I started to ween myself off of coffee a week before I started this, so I wouldn't have the caffeine withdrawal headache that we all love so much. While I am fasting I am doing a hyperbaric dive every day. It is also said that after five days of fasting your body is at the highest of making its own stem cells to heal. On the fifth day is when I will get the stem cell infusion! Disclaimer because this is fast mimicking I am not starving myself and I am not doing it do weightloss, only doing it because it is proven to help the healing process. Because when your body is not focused on constantly digestive food it has energy to heal on the cellular level. The man who has created this ProLon fast mimicking diet is Valter Longo ( if you are interested).
My mom and I have done a lot of research on fasting and there are so many benefits to it! There are also many different types of fasting and is something that everyone should try for health reasons or to just be a healthier more focused person. There is a documentary on Netflix or maybe it is amazon prime, called Fasting and it goes over the different types of fasts and follows real people on how they have changed their lives doing a fast. The video includes seven types of fasts: Time-Restricted Feeding, Intermittent and Prolonged Fasting, Long Term Water Fasting, Juice Fasting, Religious Fasting, and what I am doing Fasting Mimicking Diet. It also goes over some of the unsafety, but I am only doing this for seven days and it transitions you back into a normal diet. I am excited about this because there have been may good results from people just even for improved energy levels and brain function.
I am also excited because my very loving family has said that they would try to follow some of the protocol with me (mainly dinner and they would at least cut back on caffeine) to support me throughout the journey. Fingers crossed and prayers that my stem cells start working for healing on my brain, and if not that at least increased energy and mental clarity. PS. four hyperbaric treatments down, and about six more to go before the infusion.
My mom and I have done a lot of research on fasting and there are so many benefits to it! There are also many different types of fasting and is something that everyone should try for health reasons or to just be a healthier more focused person. There is a documentary on Netflix or maybe it is amazon prime, called Fasting and it goes over the different types of fasts and follows real people on how they have changed their lives doing a fast. The video includes seven types of fasts: Time-Restricted Feeding, Intermittent and Prolonged Fasting, Long Term Water Fasting, Juice Fasting, Religious Fasting, and what I am doing Fasting Mimicking Diet. It also goes over some of the unsafety, but I am only doing this for seven days and it transitions you back into a normal diet. I am excited about this because there have been may good results from people just even for improved energy levels and brain function.
I am also excited because my very loving family has said that they would try to follow some of the protocol with me (mainly dinner and they would at least cut back on caffeine) to support me throughout the journey. Fingers crossed and prayers that my stem cells start working for healing on my brain, and if not that at least increased energy and mental clarity. PS. four hyperbaric treatments down, and about six more to go before the infusion.
Tuesday, February 18, 2020
Hyperbaric Education 👩🏼🏫👍🏻
I almost feel like I could be a part of the
hyperbaric oxygen therapy (HBOT) team at my doctor's office because I have done so many HBOT treatments (50+ I even have an honorary dive team shirt). When I was doing these regularly I felt very
good after the treatments and know that they are worth the time and expense. Today was my first Hyperbaric treatment in a really
long time. Hyperbaric is what helped my arm to heal faster when I broke it in
2016 and is what has helped me be able to move to stay as active in school and
training as I have been. Hyperbaric treatments consist of getting zipped up in
what looks like an oversized sleeping bag. It looks intimidating at first when
you hear that you are going to be laying in a giant bag for an hour, but they
give you a walkie-talkie if you need to get out, but more importantly, this
treatment gives your body a chance to relax and heal due to the oxygen being
forced into your body. I fall asleep or do homework because it is pretty roomy.
1 down 9 more to go
I have had
these before, but this is to help get my body to get back to the level it was
at before, now in preparation for the placental cells. The pressure and the
extra oxygen speed up the healing process and reduce inflammation (which in my
case benefits my brain). The process consists of getting into the chamber, they
have an oxygen mask that you can put on for extra O2, and they pressurize the
"cabin" that fills with more air to give your body the feeling of being
taken down to sea level so you are breathing medical grade oxygen at higher
than normal pressures. You basically are breathing oxygen you'd get from a
doctor's office, two to three atmospheres "underwater" for about an
hour (PSA your ears pop a lot until you are used to it). I was doing very well physically and mentally when I was doing this
almost daily, and I know that it will help me feel good again and prepare me
for the stem cells. Once you are in the chamber it’s an hour to unwind and
sleep (I did that in the past even to the point of snoring) or listen to music
and read.
1 down 9 more to go
Me getting in 🥳
My mom not knowing how to take a picture ❤️
Studying and sleeping begins 🥱
HBOT is the use of pressure and oxygen to help heal, repair damaged tissue, and optimize health. HBOT allows us to deliver much more oxygen to the body's cells than normal. This extra O2 infusion supercharges the healing process, boosts recovery, and reduces inflammation. It provides oxygen to areas in the body where there may be limited supply due to poor circulation or injury. Hyperbarics have been found to increase vascular health, improve energy levels, enhance immune function, and regenerate tissue by releasing stem cells. Whether it's a specific health condition or general wellness and prevention, Hyperbaric Oxygen Therapy can help you.
HBOT is the use of pressure and oxygen to help heal, repair damaged tissue, and optimize health. HBOT allows us to deliver much more oxygen to the body's cells than normal. This extra O2 infusion supercharges the healing process, boosts recovery, and reduces inflammation. It provides oxygen to areas in the body where there may be limited supply due to poor circulation or injury. Hyperbarics have been found to increase vascular health, improve energy levels, enhance immune function, and regenerate tissue by releasing stem cells. Whether it's a specific health condition or general wellness and prevention, Hyperbaric Oxygen Therapy can help you.
HBOT is the use of pressure and oxygen to help heal, repair damaged tissue, and optimize health. HBOT allows us to deliver much more oxygen to the body's cells than normal. This extra O2 infusion supercharges the healing process, boosts recovery, and reduces inflammation. It provides oxygen to areas in the body where there may be limited supply due to poor circulation or injury. Hyperbarics have been found to increase vascular health, improve energy levels, enhance immune function, and regenerate tissue by releasing stem cells. Whether it's a specific health condition or general wellness and prevention, Hyperbaric Oxygen Therapy can help you.
Monday, February 17, 2020
Starting AGAIN 🧠
The following is a post from my mom's Facebook page. The response from people has been really overwhelming and humbling. Today it is with gratitude that I am beginning a treatment program, and I will be starting to post updates on how I am doing on my blog. I have a positive outlook on this treatment and am ready to take back my life so that I can feel good again. This treatment offers something very new and promising for individuals with chronic pain.
January 17, 2020
Dear friends and family,
So many people have asked us for updates on Malia and for a long time we haven’t had much to say. In all honestly, November and December were rough months for her. I did not get too many Christmas cards out, and I was going to try to do that today, but this feels easier. Thank you for your cards and well wishes and know that they are returned in our hearts. I will try to make this long, complicated story short. We moved Malia’s treatment to Cedars Sinai in December. We've seen the head of neurology twice. She thinks that she is going to diagnose Malia.
So many people have asked us for updates on Malia and for a long time we haven’t had much to say. In all honestly, November and December were rough months for her. I did not get too many Christmas cards out, and I was going to try to do that today, but this feels easier. Thank you for your cards and well wishes and know that they are returned in our hearts. I will try to make this long, complicated story short. We moved Malia’s treatment to Cedars Sinai in December. We've seen the head of neurology twice. She thinks that she is going to diagnose Malia.
It isn't great news and it's not with something we've never heard of. The diagnosis is more of a determination of what she does not have, but it still opens treatment options and with an actual diagnosis she may be eligible for clinical trials. I'm sure you are asking what is it that she has? Well, it's called MOG which stands for Myelin-oligodendrocyte glycoprotein. It means that she has an antibody to myelin. There is a lot of money going into research and hopefully new drugs will be coming. In the meantime, our doctor in Thousand Oaks who has treated Malia for Lyme, did a test last month (when she was so bad) to see if there was some DNA of anything in the blood (such as viruses, fungi, bacteria, etc.) and that test came back clean. When I talked to him about this new diagnosis, he agreed it could be that, and had some new treatment options for her to explore. All of which are expensive and are not covered by insurance. Malia has asked us to stop throwing our money away on her, but she’s our sweet girl and we can’t until we find something that will help her feel better, function better or cure her.
Please know that we have done everything that we can. We have seen every type of doctor and alternative doctor, tried every crazy and not so crazy treatment. (God bless her- she’s willing to try them.) Malia cannot be tested for almost anything because she takes prednisone and she does not make her own Ig (which is what doctors test for). In fact, she did not test positive for MOG – but it is the only plausible diagnosis that the doctors can find. She gets an IV treatment once a month called IVIg which is 1,000 people’s immunity. (Thank you to people who donate blood.)
The money that our friends and family gave five years ago went towards us taking Malia to the Mayo Clinic. Although we did not get “answers” while we were there, that is where this diagnosis originated. Her doctor at Cedars has asked us to join the Guthrie Jackson Foundation, which is for a different but similar condition. We hope to make connections and that Malia will benefit from the research they are funding.
I feel we are in a good place. We are not moving forward by leaps and bounds, but it feels like progress. She is hoping to try some new prescription medication to help her feel better in the short term as well. Doctors move slow. The daily struggle is a lot sometimes and it's getting harder for her to put on a brave face. God bless her she does. No one could be stronger and withstand what she has been through with less complaint. This has gone on since December of 2013, with Malia spending every holiday of 2014 (except Christmas) in the hospital. Thank God that’s been the last hospitalization, not that there have not been close calls.
I know that we could not keep putting one foot in front of another each day without your constant prayers for her. When I get down and wonder where God is in all of this, I imagine what if He wasn’t here in all of this. Thank you – we couldn’t do it without your faith, love and support.
Finally, Tom’s friend is a member of Kiwanians – a service organization with a mind for children – they have started a GoFundMe campaign for her. The money will go towards her treatment. We did not ask for their help, but we cannot afford to turn it down. We are grateful that there are individuals with the heart and means to help children like Malia. We have already asked our friends and family and have been so blessed by you that we would not ask you again. However, if you are interested here is the link www.gofundme.com/f/support-malia-hassenbein-in-her-fight-fo…
I appreciate your interest and support. God bless you.
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