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![]() | The contents of the Congenital lymphedema page were merged into Lymphedema on 16 August 2016. For the contribution history and old versions of the redirected page, please see its history; for the discussion at that location, see its talk page. |
I would like to also point out that primary lymphedema is lymphedema that patients are born with and can be full body lymphedema as well with swelling in all extremedies, trunk, abdomen, face, neck and other areas of the body. Lymphedema is not always confined to just one area or limb in many people.
I would like to also point out that lymphedema can be and is disabling and progressive no matter how much a patient is compliant. There are many other conditions that go hand in hand with lymphedema as well such as high blood pressure, thyroid issues, ect and these can be found in "Silent Waves" by Dr. Chikly.
The best source for patients is to educate themselves and to challenge any questionable information found on the web about lymphedema. You may use my site, http://www.lymphland.com as a link or resource.
Tinabudde 00:48, 3 September 2007 (UTC)Thanks, Tina Budde
I have added additional information on staging and grades, as well as a couple of sources. The elephantiasis described in Stage 4 may be what the previous poster might have indicated by "full body" Lymphedema. Erzahler 22:35, 21 February 2006 (UTC)
Notice: When making an entry, please indicate what entry or change you are making and the purpose of that change, and document that change in the discussion page. Because this is a medical entry, ANY CHANGE MADE TO THE TEXT THAT CANNOT BE VERIFIED WILL BE REMOVED. Erzahler 18:45, 13 March 2006 (UTC)
Erzahler,You deleted my post on Kinesio Taping, citing it wasn't recognized by NLN. It is now taught by Vodder http://www.vodderschool.com/therapists/training.cfm That is a widely accepted source of expertise also. Do you oppose it being posted as a citation? Azskeptic 01:51, 16 August 2006 (UTC)
No, I am not opposed to the information being posted if it can be verified and if it is recognized as a legitimate form of treatment. If the information is legitimate, then please post it, along with whatever qualifying information you feel is needed. A few people in the past have posted information that could not be verified or checked, which is why I prefer everything to be verifiable. Also, please include a brief statement of the addition in the edit summary. Again, I am not opposed to the posting of verifiable information, as long as it is not dubious in origin. Erzahler 15:41, 16 August 2006 (UTC)
Ace(r) wrap. I know Ace has the most recognized brand name, but that style, Ace(r), is odd. Perhaps it could be substituted with "compression wrap" or something similar. Is there a better term? -- Kevin L'Huillier 02:44, 20 August 2006 (UTC)
The Ace(r) wrap you're referring to is a long-stretch bandage and is not useful for compression wrapping as it can't provide the necessary compression without cutting off blood flow. I believe the term you're looking for is "compression bandage." Many people do use the term "compression wrap" so the two are most likely interchangeable. Erzahler 20:12, 22 August 2006 (UTC)
I've been a lympedema sufferer for the past 3 years, following an infection. I'm questioning the information below: "Stage 2 (spontaneously irreversible): The tissue now has a spongy consistency and is "non pitting" -- when pressed by the fingertips, the tissue bounces back without any indentation. Fibrosis found in Stage 2 Lymphedema marks the beginning of the hardening of the limbs and increasing size." I was in this stage for a long time but I would not now say this is "irreversible". Weekly intensive MLD treatments broke down the fibrosis for me. At first it returned, but after a few weeks of treatment, it no longer returned and has not done so for the past year. I haven't changed anything in the article, I just put this for your consideration. Janeybee 11:32, 1 April 2007 (UTC)
Thank you to the person who posted this article – a great service!
That being said, I would like to make a couple of suggestions that as a technologically-challenged layperson I don’t feel qualified to make myself:
- most of what is currently in the “Symptoms” section refers to symptoms of infection, not of LE as such, and might better be moved to a new “Complications” section, noting at the same time the need to seek medical attention for infections
- specifics could be added to the skin care section (scrupulous cleanliness using soapless cleanser, moisturization etc.).
Hope this helps!
I don't think that this statement - "Some cases of lower-limb Lymphedema have been associated with the use of Tamoxifen, due to the blood clots and deep vein thrombosis (DVT) that can be caused by this medication." - can be correct. DVT will cause venous insufficiency by damaging venous valves, and subsequent oedema, but will not cause *lymph*oedema of itself, as is does not affect the lymphatic system. Iscoed 07:58, 13 September 2006 (UTC)
Erzahler 16:58, 13 September 2006 (UTC)
About halfway down this page there's some excellent images. However in the bottom series, the 2 photos on the right hand side don't show up for me, Image:100_0587.JPG and Image:100_0583.JPG. However if I look for them it looks like they're still there. Any thoughts? The images are pretty big, maybe they need boxing in somehow?-- PaulWicks 18:25, 15 October 2006 (UTC)
The images in question show up just fine in my browser. They are smaller images, so maybe your browser is having trouble resolving them? Erzahler 18:23, 17 October 2006 (UTC)
The images are more characteristic of lipidema than lymphedema since swelling is spared in the feet. In general lymphedema gives swelling in the feet (below the ankles), but in lipidema the feet are roughly normal which is the case in these images. I strongly believe the user who posted those pictures of herself was misdiagnosed. She has lipidema Drselahi ( talk) 05:20, 16 April 2008 (UTC)
Okay, people, we need to have a little discussion here. Unless we can provide an undeniable reason why the certification links are being removed, we need to reinstate them. Regardless of the website's commercial content, these organizations provide legitimate Lymphedema certifications which are recognized by the medical community. Indeed, physical therapists cannot practice Lymphedema therapy without one of these certifications. So let's stop this senseless back-and-forth reverting/re-reverting of these links and come to a concensus on this. Being a Lymphedema patient myself and having researched this topic, I believe I do have some knowledge in this area. Erzahler 02:40, 21 October 2006 (UTC)
Awien 17:42, 21 October 2006 (UTC)
WP:EL is clear on the point that Wikipedia articles shouldn't be a forest of external links - and that furthermore, Wikipedia doesn't exist in order to stimulate trade. Nevertheless, we do happen to have a section in this article entitled "Lymphedema Product Suppliers". WP:EL states further that if there is any doubt as to the usefulness of a set of external links, it should then be put to Wikipedia editors to come to a conclusion as to how useful such a set of links actually is. PaulWicks suggests that someone who is suffering from lymphedema (or someone who is struggling to know what to do when treating someone with lymphedema) would Google the term first, and then probably consult a statutory body. However, treatment of lymphedema (and even bare recognition of the condition) is still at an early stage of development. Google presents a real forest of external links - and members of statutory bodies themselves need, perhaps, as much help as they can get. Lymphedema is complicated! I believe that people with the condition, and healthcare professionals struggling to find out how to treat it, might welcome assistance from all responsible quarters. But what do others think? Is there really a place for the section "Lymphedema Product Suppliers" or not? Should it stay or should it go? Perhaps links to patient support networks, and bodies like the British Lymphology Society are enough? Ottershrew 13:46, 2 April 2007 (UTC)
I'm not sure, maybe I should have added weasel words instead of NPOV, but I suspect my tag will be yanked promptly anyhow. Please, try to keep articles from sounding like they are about the latest new "unrecognized" disease that everyone has, like http://www.cabrillo.edu/~pkaplan/misc/lackofwater.html (yet another "75% are chronically dehydrated" myth page). I don't claim to know anything about this, and it is clear people are already watching to make sure information here is verifiable, so I'm limiting my comments to tone. The entry section in particular reads in a rather alarmist manner, or at least that is how I read it. Perhaps others react differently. Please do not be insulted by this, I'm not saying anyone is wrong in their facts. I simply feel the tone is wrong for wikipedia, that it is presenting only the view of the admittedly small portion of medical community that recognizes this. That does NOT make it fake: look how long it took for AIDS to be generally recognized, or think back to doctors saying smoking is GOOD for you, just consider your tone please. I had also tagged it with lacking references but promptly removed that. I do feel it needs a great deal more support in references to make the case. Thank you. Fitzhugh 02:25, 29 August 2007 (UTC)
External links on Wikipedia are supposed to be "encyclopedic in nature" and useful to a worldwide audience. Please read the external links policy (and perhaps the specific rules for medicine-related articles) before adding more external links.
The following kinds of links are inappropriate:
I realize that some links are "helpful to patients," but they still do not comply with Wikipedia policy, and therefore must not be included in the article. WhatamIdoing ( talk) 05:25, 17 January 2008 (UTC)
Deleted. This is Wiki, not Yahoo Answers.
What medical professional does one consult if suspicious of lymphedema? Endocrinologist? One should consult their primary care provider. The primary care provider may refer to a specialist, such a doctor who specializes in physical medicine and rehabilitation (a physiatrist).
Please say more about treatment of abdominal lymphedema. I had a friend with that. When he got in the hospital, they put him on dialysis and he lost 200 lbs in 3 weeks.
How is lymphedema associated with kidney failure? Or is the abdominal fluid from kidney failure different? —Preceding unsigned comment added by 173.56.108.58 ( talk) 14:45, 27 July 2009 (UTC) I think you may be thinking of ascites, which is a collection of fluid in the peritoneal space within the abdomen. It is commonly caused by liver failure, but can also be caused by some types of kidney disease when there is retention of sodium (which increases the amount of fluid in the body) and loss of albumin (which increases the amount of fluid that is in the extravascular space. There are lots of other causes and this is probably beyond the scope of this article.
For many years, breast cancer surgeons advised patients not to lift more than 15 pounds with the arm affected by lymph node removal due to breast cancer treatment. New studies show that women who exercise and use the affected arm are less likely to suffer lymphedema. Of course, the new information seems to be much more logical than the previous recommendations that advised to limit exercise and activity. The activity would seem to keep the lymph liquids moving and lymph tissue healthier. Massage of the arm also seems to be beneficial. —Preceding unsigned comment added by 173.57.190.183 ( talk) 02:53, 7 September 2009 (UTC)
![]() | This article is rated B-class on Wikipedia's
content assessment scale. It is of interest to the following WikiProjects: | |||||||||||||||||||||||
|
![]() | Ideal sources for Wikipedia's health content are defined in the guideline
Wikipedia:Identifying reliable sources (medicine) and are typically
review articles. Here are links to possibly useful sources of information about Lymphedema.
|
![]() | This article is prone to spam. Please monitor the References and External links sections. |
![]() | The contents of the Congenital lymphedema page were merged into Lymphedema on 16 August 2016. For the contribution history and old versions of the redirected page, please see its history; for the discussion at that location, see its talk page. |
I would like to also point out that primary lymphedema is lymphedema that patients are born with and can be full body lymphedema as well with swelling in all extremedies, trunk, abdomen, face, neck and other areas of the body. Lymphedema is not always confined to just one area or limb in many people.
I would like to also point out that lymphedema can be and is disabling and progressive no matter how much a patient is compliant. There are many other conditions that go hand in hand with lymphedema as well such as high blood pressure, thyroid issues, ect and these can be found in "Silent Waves" by Dr. Chikly.
The best source for patients is to educate themselves and to challenge any questionable information found on the web about lymphedema. You may use my site, http://www.lymphland.com as a link or resource.
Tinabudde 00:48, 3 September 2007 (UTC)Thanks, Tina Budde
I have added additional information on staging and grades, as well as a couple of sources. The elephantiasis described in Stage 4 may be what the previous poster might have indicated by "full body" Lymphedema. Erzahler 22:35, 21 February 2006 (UTC)
Notice: When making an entry, please indicate what entry or change you are making and the purpose of that change, and document that change in the discussion page. Because this is a medical entry, ANY CHANGE MADE TO THE TEXT THAT CANNOT BE VERIFIED WILL BE REMOVED. Erzahler 18:45, 13 March 2006 (UTC)
Erzahler,You deleted my post on Kinesio Taping, citing it wasn't recognized by NLN. It is now taught by Vodder http://www.vodderschool.com/therapists/training.cfm That is a widely accepted source of expertise also. Do you oppose it being posted as a citation? Azskeptic 01:51, 16 August 2006 (UTC)
No, I am not opposed to the information being posted if it can be verified and if it is recognized as a legitimate form of treatment. If the information is legitimate, then please post it, along with whatever qualifying information you feel is needed. A few people in the past have posted information that could not be verified or checked, which is why I prefer everything to be verifiable. Also, please include a brief statement of the addition in the edit summary. Again, I am not opposed to the posting of verifiable information, as long as it is not dubious in origin. Erzahler 15:41, 16 August 2006 (UTC)
Ace(r) wrap. I know Ace has the most recognized brand name, but that style, Ace(r), is odd. Perhaps it could be substituted with "compression wrap" or something similar. Is there a better term? -- Kevin L'Huillier 02:44, 20 August 2006 (UTC)
The Ace(r) wrap you're referring to is a long-stretch bandage and is not useful for compression wrapping as it can't provide the necessary compression without cutting off blood flow. I believe the term you're looking for is "compression bandage." Many people do use the term "compression wrap" so the two are most likely interchangeable. Erzahler 20:12, 22 August 2006 (UTC)
I've been a lympedema sufferer for the past 3 years, following an infection. I'm questioning the information below: "Stage 2 (spontaneously irreversible): The tissue now has a spongy consistency and is "non pitting" -- when pressed by the fingertips, the tissue bounces back without any indentation. Fibrosis found in Stage 2 Lymphedema marks the beginning of the hardening of the limbs and increasing size." I was in this stage for a long time but I would not now say this is "irreversible". Weekly intensive MLD treatments broke down the fibrosis for me. At first it returned, but after a few weeks of treatment, it no longer returned and has not done so for the past year. I haven't changed anything in the article, I just put this for your consideration. Janeybee 11:32, 1 April 2007 (UTC)
Thank you to the person who posted this article – a great service!
That being said, I would like to make a couple of suggestions that as a technologically-challenged layperson I don’t feel qualified to make myself:
- most of what is currently in the “Symptoms” section refers to symptoms of infection, not of LE as such, and might better be moved to a new “Complications” section, noting at the same time the need to seek medical attention for infections
- specifics could be added to the skin care section (scrupulous cleanliness using soapless cleanser, moisturization etc.).
Hope this helps!
I don't think that this statement - "Some cases of lower-limb Lymphedema have been associated with the use of Tamoxifen, due to the blood clots and deep vein thrombosis (DVT) that can be caused by this medication." - can be correct. DVT will cause venous insufficiency by damaging venous valves, and subsequent oedema, but will not cause *lymph*oedema of itself, as is does not affect the lymphatic system. Iscoed 07:58, 13 September 2006 (UTC)
Erzahler 16:58, 13 September 2006 (UTC)
About halfway down this page there's some excellent images. However in the bottom series, the 2 photos on the right hand side don't show up for me, Image:100_0587.JPG and Image:100_0583.JPG. However if I look for them it looks like they're still there. Any thoughts? The images are pretty big, maybe they need boxing in somehow?-- PaulWicks 18:25, 15 October 2006 (UTC)
The images in question show up just fine in my browser. They are smaller images, so maybe your browser is having trouble resolving them? Erzahler 18:23, 17 October 2006 (UTC)
The images are more characteristic of lipidema than lymphedema since swelling is spared in the feet. In general lymphedema gives swelling in the feet (below the ankles), but in lipidema the feet are roughly normal which is the case in these images. I strongly believe the user who posted those pictures of herself was misdiagnosed. She has lipidema Drselahi ( talk) 05:20, 16 April 2008 (UTC)
Okay, people, we need to have a little discussion here. Unless we can provide an undeniable reason why the certification links are being removed, we need to reinstate them. Regardless of the website's commercial content, these organizations provide legitimate Lymphedema certifications which are recognized by the medical community. Indeed, physical therapists cannot practice Lymphedema therapy without one of these certifications. So let's stop this senseless back-and-forth reverting/re-reverting of these links and come to a concensus on this. Being a Lymphedema patient myself and having researched this topic, I believe I do have some knowledge in this area. Erzahler 02:40, 21 October 2006 (UTC)
Awien 17:42, 21 October 2006 (UTC)
WP:EL is clear on the point that Wikipedia articles shouldn't be a forest of external links - and that furthermore, Wikipedia doesn't exist in order to stimulate trade. Nevertheless, we do happen to have a section in this article entitled "Lymphedema Product Suppliers". WP:EL states further that if there is any doubt as to the usefulness of a set of external links, it should then be put to Wikipedia editors to come to a conclusion as to how useful such a set of links actually is. PaulWicks suggests that someone who is suffering from lymphedema (or someone who is struggling to know what to do when treating someone with lymphedema) would Google the term first, and then probably consult a statutory body. However, treatment of lymphedema (and even bare recognition of the condition) is still at an early stage of development. Google presents a real forest of external links - and members of statutory bodies themselves need, perhaps, as much help as they can get. Lymphedema is complicated! I believe that people with the condition, and healthcare professionals struggling to find out how to treat it, might welcome assistance from all responsible quarters. But what do others think? Is there really a place for the section "Lymphedema Product Suppliers" or not? Should it stay or should it go? Perhaps links to patient support networks, and bodies like the British Lymphology Society are enough? Ottershrew 13:46, 2 April 2007 (UTC)
I'm not sure, maybe I should have added weasel words instead of NPOV, but I suspect my tag will be yanked promptly anyhow. Please, try to keep articles from sounding like they are about the latest new "unrecognized" disease that everyone has, like http://www.cabrillo.edu/~pkaplan/misc/lackofwater.html (yet another "75% are chronically dehydrated" myth page). I don't claim to know anything about this, and it is clear people are already watching to make sure information here is verifiable, so I'm limiting my comments to tone. The entry section in particular reads in a rather alarmist manner, or at least that is how I read it. Perhaps others react differently. Please do not be insulted by this, I'm not saying anyone is wrong in their facts. I simply feel the tone is wrong for wikipedia, that it is presenting only the view of the admittedly small portion of medical community that recognizes this. That does NOT make it fake: look how long it took for AIDS to be generally recognized, or think back to doctors saying smoking is GOOD for you, just consider your tone please. I had also tagged it with lacking references but promptly removed that. I do feel it needs a great deal more support in references to make the case. Thank you. Fitzhugh 02:25, 29 August 2007 (UTC)
External links on Wikipedia are supposed to be "encyclopedic in nature" and useful to a worldwide audience. Please read the external links policy (and perhaps the specific rules for medicine-related articles) before adding more external links.
The following kinds of links are inappropriate:
I realize that some links are "helpful to patients," but they still do not comply with Wikipedia policy, and therefore must not be included in the article. WhatamIdoing ( talk) 05:25, 17 January 2008 (UTC)
Deleted. This is Wiki, not Yahoo Answers.
What medical professional does one consult if suspicious of lymphedema? Endocrinologist? One should consult their primary care provider. The primary care provider may refer to a specialist, such a doctor who specializes in physical medicine and rehabilitation (a physiatrist).
Please say more about treatment of abdominal lymphedema. I had a friend with that. When he got in the hospital, they put him on dialysis and he lost 200 lbs in 3 weeks.
How is lymphedema associated with kidney failure? Or is the abdominal fluid from kidney failure different? —Preceding unsigned comment added by 173.56.108.58 ( talk) 14:45, 27 July 2009 (UTC) I think you may be thinking of ascites, which is a collection of fluid in the peritoneal space within the abdomen. It is commonly caused by liver failure, but can also be caused by some types of kidney disease when there is retention of sodium (which increases the amount of fluid in the body) and loss of albumin (which increases the amount of fluid that is in the extravascular space. There are lots of other causes and this is probably beyond the scope of this article.
For many years, breast cancer surgeons advised patients not to lift more than 15 pounds with the arm affected by lymph node removal due to breast cancer treatment. New studies show that women who exercise and use the affected arm are less likely to suffer lymphedema. Of course, the new information seems to be much more logical than the previous recommendations that advised to limit exercise and activity. The activity would seem to keep the lymph liquids moving and lymph tissue healthier. Massage of the arm also seems to be beneficial. —Preceding unsigned comment added by 173.57.190.183 ( talk) 02:53, 7 September 2009 (UTC)