The information available on the Breast Cancer Network Australia website is not medical advice and is provided for information purposes only. It should not be viewed as a replacement for a consultation with a qualified medical professional. Our website is designed to offer information and support to the general public. Be aware that we do not provide any medical advice, and for medical advice we recommend you speak to a qualified medical professional or doctor. 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and frustrating! ***Rant warning***","id":"message:138289","revisionNum":1,"repliesCount":14,"author":{"__ref":"User:user:757"},"depth":0,"hasGivenKudo":false,"board":{"__ref":"Forum:board:general-lifestyle-and-wellbeing"},"conversation":{"__ref":"Conversation:conversation:138289"},"readOnly":false,"editFrozen":false,"moderationData":{"__ref":"ModerationData:moderation_data:138289"},"body@stripHtml({\"truncateLength\":200})":" I'm ten months post surgery, four months post chemo and finished rads at the end of May. My health has generally improved--I don't feel 'sick' any more, but I'm struggling with lymphedema in one 'foo...","body@stringLength":"2361","rawBody":"
I'm ten months post surgery, four months post chemo and finished rads at the end of May. My health has generally improved--I don't feel 'sick' any more, but I'm struggling with lymphedema in one 'foob', cording and scar tissue in my armpit, tendonitis and myalgia in both legs and feet and now lymphedema is setting up camp in one leg. So I'm not exactly 'well'.
I finally managed to get access to a physio (please don't recommend I see an EP, there isn't one within 150 km) and between her efforts and mine, I'm doing the best I can. Low and behold another physio pops up at the hospital where my oncologist is based (over 100km away) with an appointment time, so I went to see her.
I'm running out of options through our local community care facility which has very limited resources, I explained this to physio 2 and we went through the exercise program I'm doing at home. \"Well' she says \"Since you are trying to self manage, perhaps we can access some short term funding through our Community Interlink program.\" This is a little pot of money which can fund programs for people in my situation. She approached them for funding for a 6 month pool pass for me. I like to swim, it gets the weight off my feet and would help with the lymphedema, the pool is 20km away, but it costs. I'm only working two days a week and haven't got much to spare at the moment.
I thought this was a great idea, then the frustration started. Her hospital won't fund me because--even though I surgery and chemo there--I live here which is outside their catchment area. The funding model here has changed because they are moving to NDIS, so to access the money I have to meet the criteria of the disability act. As some of you know, getting classified as disabled is not that easy. AND I DON'T WANT TO DO IT!
The irony. I can't get the help I need to avoid becoming disabled, because I'm not yet classified as disabled. What hoo-haa.
Now I'm being offered a bit more physio (depending on availability) if I will travel over there to get it. How much do they think that will cost when lined up against a $400 pool pass that could genuinely make a difference? This sort of bullshit costs the health service millions and millions. Yes, I know there are rules, but the rule makers need a kick up the arse.
I'm ten months post surgery, four months post chemo and finished rads at the end of May. My health has generally improved--I don't feel 'sick' any more, but I'm struggling with lymphedema in one 'foob', cording and scar tissue in my armpit, tendonitis and myalgia in both legs and feet and now lymphedema is setting up camp in one leg. So I'm not exactly 'well'.
I finally managed to get access to a physio (please don't recommend I see an EP, there isn't one within 150 km) and between her efforts and mine, I'm doing the best I can. Low and behold another physio pops up at the hospital where my oncologist is based (over 100km away) with an appointment time, so I went to see her.
I'm running out of options through our local community care facility which has very limited resources, I explained this to physio 2 and we went through the exercise program I'm doing at home. \"Well' she says \"Since you are trying to self manage, perhaps we can access some short term funding through our Community Interlink program.\" This is a little pot of money which can fund programs for people in my situation. She approached them for funding for a 6 month pool pass for me. I like to swim, it gets the weight off my feet and would help with the lymphedema, the pool is 20km away, but it costs. I'm only working two days a week and haven't got much to spare at the moment.
I thought this was a great idea, then the frustration started. Her hospital won't fund me because--even though I surgery and chemo there--I live here which is outside their catchment area. The funding model here has changed because they are moving to NDIS, so to access the money I have to meet the criteria of the disability act. As some of you know, getting classified as disabled is not that easy. AND I DON'T WANT TO DO IT!
The irony. I can't get the help I need to avoid becoming disabled, because I'm not yet classified as disabled. What hoo-haa.
Now I'm being offered a bit more physio (depending on availability) if I will travel over there to get it. How much do they think that will cost when lined up against a $400 pool pass that could genuinely make a difference? This sort of bullshit costs the health service millions and millions. Yes, I know there are rules, but the rule makers need a kick up the arse.
"},"Conversation:conversation:138289":{"__typename":"Conversation","id":"conversation:138289","solved":false,"topic":{"__ref":"ForumTopicMessage:message:138289"},"lastPostingActivityTime":"2017-08-06T18:01:54.000-07:00","lastPostTime":"2017-08-06T18:01:54.000-07:00","unreadReplyCount":14,"isSubscribed":false},"ModerationData:moderation_data:138289":{"__typename":"ModerationData","id":"moderation_data:138289","status":"APPROVED","rejectReason":null,"isReportedAbuse":false,"rejectUser":null,"rejectTime":null,"rejectActorType":null},"Revision:revision:138289_1":{"__typename":"Revision","id":"revision:138289_1","lastEditTime":"2017-08-02T21:06:58.000-07:00"},"ForumReplyMessage:message:138292":{"__typename":"ForumReplyMessage","id":"message:138292","conversation":{"__ref":"Conversation:conversation:138289"},"author":{"__ref":"User:user:15050"},"revisionNum":1,"uid":138292,"depth":1,"hasGivenKudo":false,"subscribed":false,"board":{"__ref":"Forum:board:general-lifestyle-and-wellbeing"},"subject":"Re: Riduculous and frustrating! ***Rant warning***","readOnly":false,"editFrozen":false,"moderationData":{"__ref":"ModerationData:moderation_data:138292"},"parent":{"__ref":"ForumTopicMessage:message:138289"},"body":"Hi Zoffiel Do you have a masseur near you ? Hopefully one that has studied some remedial work as well. You need help to get the cording 'cracked' (your physio should do that easily) and then if the masseur can use some silicone Chinese cups (and bio-oil) to get the fluid on the move you will get a lot of relief from the lymphoedema. Hubby did learn to use them and that was great but with his dementia that option is lost for me - I don't know your circumstances but perhaps that is an option ? I can put you in touch with a supplier of the cups - they are in Melbourne but you can order on-line like I did). Good luck Summer :-)","body@stringLength":"683","rawBody":"Hi Zoffiel Do you have a masseur near you ? Hopefully one that has studied some remedial work as well. You need help to get the cording 'cracked' (your physio should do that easily) and then if the masseur can use some silicone Chinese cups (and bio-oil) to get the fluid on the move you will get a lot of relief from the lymphoedema. Hubby did learn to use them and that was great but with his dementia that option is lost for me - I don't know your circumstances but perhaps that is an option ? I can put you in touch with a supplier of the cups - they are in Melbourne but you can order on-line like I did). Good luck Summer :-)","kudosSumWeight":0,"repliesCount":0,"postTime":"2017-08-02T22:23:26.000-07:00","images":{"__typename":"AssociatedImageConnection","edges":[],"totalCount":0,"pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null}},"attachments":{"__typename":"AttachmentConnection","pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null},"edges":[]},"timeToRead":1,"currentRevision":{"__ref":"Revision:revision:138292_1"},"latestVersion":null,"metrics":{"__typename":"MessageMetrics","views":0},"visibilityScope":"PUBLIC","isEscalated":null,"placeholder":false,"originalMessageForPlaceholder":null,"messagePolicies":{"__typename":"MessagePolicies","canModerateSpamMessage":{"__typename":"PolicyResult","failureReason":{"__typename":"FailureReason","message":"error.lithium.policies.feature.moderation_spam.action.moderate_entity.allowed.accessDenied","key":"error.lithium.policies.feature.moderation_spam.action.moderate_entity.allowed.accessDenied","args":[]}}},"customFields":[],"replies":{"__typename":"MessageConnection","edges":[],"pageInfo":{"__typename":"PageInfo","hasNextPage":false,"endCursor":null,"hasPreviousPage":false,"startCursor":null}}},"CachedAsset:theme:customTheme1-1743643614981":{"__typename":"CachedAsset","id":"theme:customTheme1-1743643614981","value":{"id":"customTheme1","animation":{"fast":"150ms","normal":"250ms","slow":"500ms","slowest":"750ms","function":"cubic-bezier(0.07, 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