Wednesday, 27 February 2013

Harvest Belongings


 

Lateral venting harvest Belongings: Lymphoma Cancer
Let me first say that this is in no way intended, apply to the products that we use to buy our little Emma. I write this to you. An idea of ​​what we have done and what all side effects that have told us that a part of their treatment would work Ca
this are our history. On 2 July 2010, my wife Emma (four and a half years was at the time). To a doctor's appointment because h Harvest Belongings Cancere looked a little pale, and made some points in the neck, which is not normal Lymphoma doctor called a pediatrician and we recommend blood tests done as soon as we could. What happened to the local hospital for 4 hours and 6 hours we were back at the hospital, where they said they had a high risk of B-lymphocytes (white blood cells high). Our lives changed in an instant, as you all know. By 21:00, my wife and daughter on the way to BC Children's Hospital had to start treatment immediately.
For work, my wife and I are working a home business that life independent distributors herbs (an international company in the fields of health and wellbeing). I say this to show certain things. This disease has no prejudice, because everyone, young, old, healthy or ill haunt. Emma has never had a serious illness and very few simple cold since birth. We started on natural supplements for children, and they have started to voluntarily morning shake every day. This proved to be a good thing, because while she was in hospital, she did not want to eat "real", but we were able to maintain their strength with good nutrition shakes. Sure, we make sure that the doctors gave, not what. Conflict with the medication he received
second, we use as our business is working online, by telephone and other simple methods, which means that it can rely on for our "work" or leave them completely with Emma had to be during this period. We have. Of many others who had heard financial problems and employment problems for this reason After talking with other parents of children in the hospital and clinic, as well as others in our community who have had children with the same disease, we decided that treatment done everything Emma undergo where care is better at Children's Hospital in British Columbia. This meant that we had to move out of the island, it was a gesture difficult, but necessary. Again, we have bothered with very little to our business (which also means that our income) performed while for Emma.
So here's what we did for Emma in the last 9 months - I cannot believe it was so long - and what happened. Every morning, she has a life meal replacement shakes grass ½ cup water and 1 cup milk. As appetite is a side effect, it is necessary to ensure that there was adequate food for the day, as it were, we would still be happy there. Another good thing is that if it. On steroids, the weight does not win because of two wishes caused by them this movement also has a large amount of energy, the doctors are very impressed. Another side effect is nausea and constipation. But she is with Herbal Aloe Concentrate - which comes in regular or mango flavor is enough for you to change when chemotherapy. It is a drinkable liquid heals and protects home and avoid other internal problems. On a visit to the clinic, they received high-dose methotrexate and decided to give a plasticizer and against our wishes, we took it. She developed blisters and burns on your ass so bad for me that was prescribed morphine pain. We increased the dose of Vaseline Aloe applied and kept clean, and in three days, delete all. The doctors and nurses are always surprised by the lack of Emma side effects and how it manages its processes. She is active and usually has a smile on her face, but she has the odd day where you get tired and bad mood because of the medicine.

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