Now I Finally got dx with LE
I have been lurking around the LE section on breastcancer.org. I found that there were no certified LE therapists near me (closest was almost 3 hours away). I have been telling my family dr.,my pain dr and nurses about LE symptoms (my breast surgeon moved away and I don't have an oncologist).
Well, this summer my lower spine was hurting so bad I could hardly move, so I started PT for that. I got curious about the others that worked there and was reading all their info cards. I stumbled upon a woman who is part of the pilot program for cancer rehab for those that had or have cancer and need PT/OT for whatever AND it includes an individual exercise program. I was talking to my back PT about it and low and behold....that lady knows LE and how to treat it.
At my last family dr. appt she wrote me a prescription for the Cancer Stepping Stones and LE. The LE therapist happened to be at the front desk when I was making my first appt (the PT dept I am using is below my family dr). She took one look at me and could see I was swollen in the arm and the side truncal area.
Today was my first appt. and yup, I have LE. She did massaging on my chest and arms. I started using the pump, too for 30 minutes. She doesn't have any sleeves in my size, so she is ordering one for me. I am so relieved to finally have found someone.
So in addition to the severe PMPS, I officially have LE that I have known I have had for a year. I also consider myself very lucky that it stayed a mild case and didn't turn severe.
So I now joined the LE club....
Comments
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I am so glad to hear that
I am so glad to hear that you found someone who HEARD you before your LE had gotten worse! I have some mild LE and I just think of it as another chronic condition. Most of the time I don't even think about it although initially I thought about it quite a bit. Hope your arm and chest area are feeling better and better! BTW, what is PMPS? xoxoxo Lynn0 -
Glad you finely found some
Glad you finely found some one to help you.
Hugs Frankie0 -
good you found out
There are a few of us on this board with Lymhedema. I sometimes think the doctors don't always have the light bulb go on in thier heads when we make certain complaints. Because many on my oncology team knew that I was doing a lot of research on my particular form of breast cancer I think it worked in my favor when I asked for something. I also think being on this board and reading so many stories from those who have gone through difficulties gave me more courage to ask for what I thought I needed. I think a good many of them knew also that I was on the ACS cancer support network. I was either really lucky or really respected when I self advocated for certain things.0 -
I don't have this, but, amlynn1950 said:I am so glad to hear that
I am so glad to hear that you found someone who HEARD you before your LE had gotten worse! I have some mild LE and I just think of it as another chronic condition. Most of the time I don't even think about it although initially I thought about it quite a bit. Hope your arm and chest area are feeling better and better! BTW, what is PMPS? xoxoxo Lynn
I don't have this, but, am happy you found someone to help you. I hope you start feeling better quickly.
Hugs, Jan0
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