Yesterday Mihaela went to the clinic at 8am and did not leave until 6pm. Long day!! First they got blood drawn to test the white blood cell count level which was at almost normal range, at about 3.8, normal is 3.9-4.00. They found that Calcium is a little low so she needs to work on that, more coconut milk (dairy has lower calcium by volume when processed in our body) and leafy greens, kale, spinach, broccoli, etc but the naturopath dr recommended some Calcium supplements also. The nutritionist was happy to learn that she gained a couple of pounds. The oncologist was pleased to see that the lymphnodes on the neck decreased significantly, where they are barely palpable (feel them) It is somewhat expected after the first treatment, but doctor seemed excited about it. Afterwards she went upstairs to infusion to get the chemo, she settled in a comfy reclining chair with a pretty good view of the dessert. First they gave the pre meds for nausea and ‘antistress’ stuff that makes you loopy and sleepy; when that is over they start with each of the 4 individual ABVD drugs at the time. It takes a total of 5-6 hours for the entire process. On the bright side they bring you food and fluids/smoothies as one pleases as Mihaela tries to eat and hydrate plenty for the body to sustain the ‘poison’! :)
Got more natural supplements to add to the ‘after treatment’ regiment to take along with the anti-nausea medications. The naturopath prescribed Co-enzyme Q10 and glutamine to help protect the body from the chemo drugs.
The doctor decided to go ahead this time with Neulasta, the shot that improves the white blood count. This should be done 24 hrs after treatment, so on Thursday at 6pm she’ll be there ready and square. It’s a shot they usually do in the belly apparently it gets absorbed in the system faster in the adipose (fatty tissue). Not looking forward to the potential side effects of bone and marrow pain/discomfort. I think they prescribed her something for that too. :)
There might be a problem with the chemo meds in the long run, it seems the clinic is keeping things low profile and do not specifically admit to that but they admit there is a national shortage of various drugs, even simpler ones. Considering the needs, as it seems now, at least 8 treatments/doses, potentially 12, we want to make sure they preorder or ensure the meds will be available. They cannot guarantee it but did say they will do all possible, of course. I guess time will tell. Here's a link from the FDA with national drug shortages
Day 1 after chemo seems OK so far. There is some residue from the loopy drugs from yesterday as she told me earlier today and she is somewhat dragging around the house. Hair started to fall but still not significant, no chunks yet. First sign of that, it will be buzzed and Mihaela will try to compete with Cipi on their best looks:)
We all hope she will feel the same, as in well and good, after this treatment as she did after the first one. From what we understood yesterday, she will feel the same throughout the treatment, as sh did after the first one, which is a good sign, because she only had a few days of feeling 'flu-like' symptoms, but nothing major or needing to stay in bed for days.
Thank you once again to your continuous support. Please feel free to share the link to this blog to anyone that might be interested.
Got more natural supplements to add to the ‘after treatment’ regiment to take along with the anti-nausea medications. The naturopath prescribed Co-enzyme Q10 and glutamine to help protect the body from the chemo drugs.
The doctor decided to go ahead this time with Neulasta, the shot that improves the white blood count. This should be done 24 hrs after treatment, so on Thursday at 6pm she’ll be there ready and square. It’s a shot they usually do in the belly apparently it gets absorbed in the system faster in the adipose (fatty tissue). Not looking forward to the potential side effects of bone and marrow pain/discomfort. I think they prescribed her something for that too. :)
There might be a problem with the chemo meds in the long run, it seems the clinic is keeping things low profile and do not specifically admit to that but they admit there is a national shortage of various drugs, even simpler ones. Considering the needs, as it seems now, at least 8 treatments/doses, potentially 12, we want to make sure they preorder or ensure the meds will be available. They cannot guarantee it but did say they will do all possible, of course. I guess time will tell. Here's a link from the FDA with national drug shortages
Day 1 after chemo seems OK so far. There is some residue from the loopy drugs from yesterday as she told me earlier today and she is somewhat dragging around the house. Hair started to fall but still not significant, no chunks yet. First sign of that, it will be buzzed and Mihaela will try to compete with Cipi on their best looks:)
We all hope she will feel the same, as in well and good, after this treatment as she did after the first one. From what we understood yesterday, she will feel the same throughout the treatment, as sh did after the first one, which is a good sign, because she only had a few days of feeling 'flu-like' symptoms, but nothing major or needing to stay in bed for days.
Thank you once again to your continuous support. Please feel free to share the link to this blog to anyone that might be interested.
