I am only one of many pensioners with worsening Lymphodema due to the cost of private Physio.
I can get 5 visits a year on Medicare ( with the lovely Jenny Pope, ex C.C.) on the Enhanced Care Plan, via GP. As I live in the Hills and need a friend to drive me, her Home Clinic 5 minutes away is perfect but not always affordable. Unfortunately a serious blockage has developed and I am not currently eligible for this years Medicare visits. She wants me to come weekly for a while to clear the blockage.
While investigating the situation with Medicare I was put through to a Cancer Nurse at the WA Health Dept. who has got me back into the S.C.G.H. Occupational Therapy Lymphodema lady. This is usually a short time service, but I will find out when I get the letter, hopefully tomorrow. It will be an hour and a half drive, but I am desperate!
Does any one else feel strongly about this HUGE gap in services? I have time to work on some ideas if we could get a few people interested to do some lobbying. This is a serious health issue that will not go away.
In Grace
Phoebe (Diploma Human Services)
This post was edited by Phoebe at March 13, 2016 12:14:59 PM WATime"
Single woman no kids, Breast Ca diagnosed 2003, lumpectomy (problematic not enough clearance around tumour so surgeon went in again after 2 weeks),auxiliary clearance, chemo, radiation, Tamoxifen for 5 yrs. at the time I went on Tamoxifen I came out in psoriasis which remains a problem.
Reconstruction 2006- Lapidimus Dorsi (back muscle used for flesh to rebuild breast) on second recon, the first recon was a big mess !!
Squamous Cell Ca on vocal chord diagnosed 2005,surgery, more surgery, radiation, more surgery, currently have lump on vocal chord being checked 6 weekly (probably damage from radiation) I am refusing further surgery on throat to preserve what is left of my voice! Long journey.
Support Services Coordinator at BCCWA