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    <title>Hand &amp; Foot Syndrome</title>
    <description>Latest messages for CancerCompass discussion</description>
    <link>http://www.cancercompass.com/message-board/message/all,30618,0.htm</link>
    <pubDate>Mon, 23 Nov 2009 00:00:00 GMT</pubDate>
    <lastBuildDate>Mon, 23 Nov 2009 00:00:00 GMT</lastBuildDate>
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      <title>RE: Hand &amp; Foot Syndrome</title>
      <description>&amp;nbsp;On 11/24/2008 j11good wrote:HelloFirst I would like to say that our God is Awesome and He gives me strength not just day by day but second by second. &amp;nbsp;I was diagnosed with the Breast &amp;quot;C&amp;quot; word about 4 years ago (actually it was this time of year), I underwent agressive chemo (ACT) and then radiation everyday for what seemed like an eternity. I was down to where I would just have to see my oncologist twice and year and started having some leg pain, well after some scans it was determined that the &amp;quot;C&amp;quot; had metastized to my bones. So I had a few more rounds of radiation on various parts of my body. Through all of this God gave me His continued strength to keep working. However, now I am taking Xeloda and have developed hand &amp;amp; foot syndrome. Has anyone expierenced this and if so do you have any suggestions to help it. It sure is painful................Thank you and God Bless to AllJ&amp;nbsp;I received Adramycin/Cytoxan and Taxol Chemotherapy also for a 6-month duration back in 2001 for early Stage II cancer (after having had a right modified radical mastectomy from a breast cancer specialist).&amp;nbsp; &amp;nbsp;I ended up with peripheral neuropathy in the hands and feet just as you are experiencing.&amp;nbsp; In addition to that, I had severe nerve damage in the chest and pain there from the surgery which has never gone away. I&amp;#39;ve had extreme pain all along in the chest, feet and hands.&amp;nbsp; When the pain peaked so badly after the ending of my chemo, I called the nurse in the oncologists office and was in tears.&amp;nbsp; I&amp;#39;d been boiling hotpacks at home and applying them to my chest and that helped for a short while.&amp;nbsp; &amp;nbsp;What might be of help to you is&amp;nbsp;NEURONTIN (Gabapentin) CAPSULES &amp;nbsp;- 300 mg.&amp;nbsp; I worked slowly and built up to 1,800 mg. per day, taking 2 at breakfast, 2 at lunch, and 2 at supper time.&amp;nbsp; These could be prescribed by your oncology office or your family doctor or internist.&amp;nbsp; &amp;nbsp;Also, my internist doctor prescribed PAMELOR&amp;nbsp;(Nortriptyline) - 25 mg. capsule - 1 at bedtime to help with&amp;nbsp;all the pain and help with sleep.&amp;nbsp; So, I&amp;#39;ve been on this regimen since 2001:&amp;nbsp; 6 Neurontin Caps per day and 1 Pamelor at night.&amp;nbsp; &amp;nbsp;&amp;nbsp;You can ask for the generic forms of these two medications and it is CHEAPER.&amp;nbsp; Generic Pamelor is Nortriptyline, and Generic Neurontin is Gabapentin. Also, I&amp;#39;ve read about something on-line recently that I&amp;#39;m exploring and you might want to read about it too. It&amp;#39;s from ReBuilder Medical, Inc.:http://www.rebuildermedical.com&amp;nbsp;&amp;nbsp;  They will send you information upon request about a device that they claim can help with the neuropathy in the feet.&amp;nbsp; I have received a small disc with information on it that I&amp;#39;ve yet to put in and play.&amp;nbsp; It is called Heartbeat of America Interview - Hosted by William Shatner. You can purchase the device on-line from ReBuilder Medical Technologies, Inc.&amp;nbsp;You can read for yourself and see what you think.&amp;nbsp; &amp;nbsp;For the pain in my chest that peaks throughout the day, I&amp;#39;ve discovered that a heavy-duty moist THERMOPHORE heating pad really helps that. I have it on several times a day when the pain peaks the worst.&amp;nbsp; I think it encourages blood circulation around the damaged nerve tissue.&amp;nbsp; The most up-dated pad has 4 blocks that turn green when you plug in the pad.&amp;nbsp; Each block is for 5 minutes duration.&amp;nbsp; The pad goes off on its own after 20 minutes total.&amp;nbsp; Or, you can turn it off on your own if you do not need all of the 20 minutes.&amp;nbsp; This pad penetrates down deeper than ordinary heating pads.&amp;nbsp; You can purchase the Thermophore on-line also or have your pharmacy order in one for you if you are interested in it.&amp;nbsp; The peripheral neuropathy you are experiencing is a result of taking TAXOL.&amp;nbsp; Have you talked with the nurse in your oncologists office or specifically your oncology doctor as well about it?&amp;nbsp; They are familiar with Neurontin which can help a lot of people like you.&amp;nbsp; There is also a new medication called LYRICA that is for neuropathy.&amp;nbsp; I tried it for three months but it was not effective for me.&amp;nbsp; If you do decide to take the Neurontin, order some Vitamin D-3 capsules from Swanson Vitamins and take one daily.&amp;nbsp; Taken long-term Neurontin can deplete Vitamin D in the body.&amp;nbsp; I&amp;#39;ve read that anticonvulsants can sometimes cause osteoporosis when taken long-term if you do not supplement with Vitamin D-3 (Cholecalciferol).&amp;nbsp; So, for that reason, I buy the High-Potency Vitamin D-3 in the 1,000 International Units size from Swanson Vitamins - Item No. SW1030 - Toll Free Number is:&amp;nbsp; 1-800-437-4148.&amp;nbsp; I&amp;#39;ve also read that Vitamin B 6 is good to take for neuropathy and I &amp;nbsp;take that as well and boost the level to 3 capsules per day.&amp;nbsp; The B-6 Item No. is SW022 at SwansonVitamins.com or at the same toll free phone number I&amp;#39;ve listed above.&amp;nbsp; The B-6 I take is 100 mg. 3 x per day (in capsule form from Swanson Vitamins.&amp;nbsp; I&amp;#39;m not sure of your age, but if you have not had a DEXA Bone Density Test, ask for one to get your baseline.&amp;nbsp; Then follow your doctor&amp;#39;s suggestion as to what intervals to redo the DEXA Bone Density Scan thereafter if you take the Neurontin ongoing.&amp;nbsp; I hope this information will be of help to you.&amp;nbsp; Do let me know how you do on the Neurontin if you take it.&amp;nbsp; Remember, you can start low and build upon it as you need it strength wise.&amp;nbsp; &amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;</description>
      <author>Patti_in_Cincinnati</author>
      <pubDate>Fri, 28 Nov 2008 00:00:00 GMT</pubDate>
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    <item>
      <title>RE: Hand &amp; Foot Syndrome</title>
      <description>&amp;nbsp;On 11/24/2008 j11good wrote:HelloFirst I would like to say that our God is Awesome and He gives me strength not just day by day but second by second. &amp;nbsp;I was diagnosed with the Breast &amp;quot;C&amp;quot; word about 4 years ago (actually it was this time of year), I underwent agressive chemo (ACT) and then radiation everyday for what seemed like an eternity. I was down to where I would just have to see my oncologist twice and year and started having some leg pain, well after some scans it was determined that the &amp;quot;C&amp;quot; had metastized to my bones. So I had a few more rounds of radiation on various parts of my body. Through all of this God gave me His continued strength to keep working. However, now I am taking Xeloda and have developed hand &amp;amp; foot syndrome. Has anyone expierenced this and if so do you have any suggestions to help it. It sure is painful................Thank you and God Bless to AllJ&amp;nbsp;hi&amp;nbsp;J try this site God bless and take care&amp;nbsp;Ray &amp;nbsp;http://pda.asco.org/patient/Diagnosis+and+Treatment/Treating+Cancer/Managing+Side+Effects/Hand-Foot+Syndrome+or+Palmar-Plantar+Erythrodysesthesia</description>
      <author>jcr65566</author>
      <pubDate>Mon, 24 Nov 2008 00:00:00 GMT</pubDate>
    </item>
    <item>
      <title>Hand &amp; Foot Syndrome</title>
      <description>HelloFirst I would like to say that our God is Awesome and He gives me strength not just day by day but second by second. &amp;nbsp;I was diagnosed with the Breast &amp;quot;C&amp;quot; word about 4 years ago (actually it was this time of year), I underwent agressive chemo (ACT) and then radiation everyday for what seemed like an eternity. I was down to where I would just have to see my oncologist twice and year and started having some leg pain, well after some scans it was determined that the &amp;quot;C&amp;quot; had metastized to my bones. So I had a few more rounds of radiation on various parts of my body. Through all of this God gave me His continued strength to keep working. However, now I am taking Xeloda and have developed hand &amp;amp; foot syndrome. Has anyone expierenced this and if so do you have any suggestions to help it. It sure is painful................Thank you and God Bless to AllJ&amp;nbsp;</description>
      <author>j11good</author>
      <pubDate>Mon, 24 Nov 2008 00:00:00 GMT</pubDate>
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