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MandaMoo's avatar
MandaMoo
Member
15 years ago

Treatment Plan

I'm now 9 days post my mastectomy and feeling better every day.  I have been very tired and lethargic but today was the first time I didn't feel the need to take anything for the pain during the day.  I even went with my Dad to go and pick two of the kids up from school.  I also visited Medicare!  I have a box full of invoices and receipts already - why does everyone do it differently?

I saw my surgeon on Tuesday and had my drain removed - boy that was ouchie - seems it was next to my nerve so irritated it when removed.  I am still getting very weird sensations in my arm, shoulder blade, armpit area - a sort of hypersensitivity - I jump 10 feet high if lightly touched on my arm or back.  My surgeon spent more than an hour going through the pathology report and our next steps - looking at my prognosis based on treatment options etc...  So we came out with a plan and a referral to see the Oncologist.

(My pathology results were 2/14 positive nodes, 3 tumors within breast - largest 2.2cm. her2+ve, Hormone receptor -ve, grade3.  I also had a 9cm wide area of DCIS. All of the tissue has been removed clearly. So we did the right thing upfront with the mastectomy)

We met my oncologist on Thursday - she was lovely, informative and I felt comfortable with her.  I am going to commence chemotherapy on the 29th of March so long as my wounds are fully healed. (I see my surgeon again in a fortnight and also have some fluid injected into my expander at the same time). I am having three rounds of FEC 100, then move onto Taxotere with herceptin (we didn't receive much info about this yet as she didn't want to overload us) and then will continue the herceptin every three weeks for a 12month period.  

I will be an inpatient overnight with the first three chemo at least - my oncologist likes to give IV fluids to ensure that the drugs are well flushed.  I am happy with this and think it may be easier on the family.  We went through the possible side effects but won't know until I experience it what it is like for me.  I have friends who have continued to work through chemo so we'll just wait and see what happens.

On the home front things are OK - there is some sort of normality in the abnormality of the moment.  My 6yo is struggling the most.  She is usually my one that nothing bothers but she is teary and scared.  She apparently had a very fragile day at school and is just finding it all a bit hard.  Tonight the three kids all fought over who would sit next to me at dinner which ended up in dinner on the floor and broken plates and of course tears...  My husband is doing OK - I thought he was fine until we saw the oncologist and he broke down again - he is finding it very hard but being so very supportive and caring.  At least tonight he managed a night out at the football. My folks will head home interstate next week when I am up to driving again and then will come back when I start chemo.  I am OK with it all but starting to resent the lack of control I have over our life at the moment.  I do snap back into form though and say "just focus" on getting this thing beat and it will be better on the other side. 

Bed is calling again - I'm not sure about this lethargy - I'm usually such a nightowl.  I hope everyone has a lovely long weekend. 

 

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