Calling all triple negative breast cancer patients in the UK
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Hello liv and BernieEllen.
I hope all is well with you. We have missed you on the thread this week.
Come back soon!
Love.
Sylvia xxxx
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Hi All,
Well it's over, I have finally finished chemo! I am so tired today as Emma was up during the night aswell. Just having a rest now. Strange feeling being finished, the safety net has been removed and now I am on my own. Going for CT Scan for alignment for rads tomorrow and will probably start rads in the next few wks. Meeting my onc on the 28th so prob after that.
Carolben I am so sorry to hear of your diagnosis - cancer is so sneaky! Trust in the Lord and you will get through this! Weekly taxol is very doable. I felt almost normal on it. Chin up and boxing gloves on...you can fight this beast!!!
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Hello Mumtobe.
Congratulations on finishing chemo. Well done. You do feel strange when you finish one treatment and are waiting for another. Try to rest as much as you can.
Thinking of you and wishing you all the very best.
Sylvia xxxx
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Hello Carolben
So sorry to hear your latest news.I find it very strange that your diagnosis has gone from DCIS to mets,and in such a short time.I must say I have never heard of chemo and rads for DCIS; I wonder whether there is something your medical team did not tell you at the time.
I have heard that weekly chemo is very doable, since the side effects are much reduced that way.As the lung nodules are small, there is a good chance the chemo will be enough to put you back into remission.
The sooner your treatment starts, the more you will feel that you have some control over what is going on.
We are all here to support you.
Hugs,
Sam
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Hello Sylvia
Well done on getting your appointment for a DEXA scan.I have beaten you to it by one day as my appointment is for the 25th February! However....I need to be with my father that day as a health professional is coming to see him, so I have changed the appointment for a couple of weeks later.I will be interested to see what your results show;I really hope we both see an amelioration in our osteoporosis.
I hope you manage to get PTH included in your blood tests; I am not sure when or how I will get the results of my blood tests, since they were ordered by the rheumatologist and I am not due to see him for another 6 months.....
I have Parent Review Meetings tomorrow, starting with one before school starts and then finishing at 7pm.Only one week after this, though, and it is half term.
I really must get started on getting the allotment ready for planting soon; it has been so wet and cold that I haven't been near the place for some time.
With love,
Sam x
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Hi Linali
I was interested to hear about your son's experiences with Aspergers; my son was diagnosed a bit earlier, but still quite late at the age of 14.He also suffered a lot of bullying and changed school a few times, being a school refuser some of the time because of the treatment of both other pupils and some of the staff.There was so much ignorance about Aspergers,that I hope has changed now.
One of the most difficult aspects is that they are intelligent and often of above-average intelligence and yet cannot cope in a 'neuro-typical' world. I can see that Leigh had an awful lot to cope with with gender disphoria as well.It is to his credit that he is able to live independently, albeit with 24hour support at the end of a phone-line.
My son, Tom, has developed epilepsy within the last 4 years, and this is impacting on his life even more than the Aspergers, since it is not being controlled.We are still hoping that he will be able to live independently at some point soon.
As you say, it is good to be in touch with people who understand.
Thank you for your good wishes,
Sam x
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Good morning to you all. I have been quite busy so please forgive me for not catching up with all that has been going on.
So sorry to hear that life is still very difficult for some of you.
I an currently on care support for my neighbour. Sadly, she has a serious flesh eating bacterial infection in her foot caused by an untreated ulcer. She is a bad diabetic and rather a large lady and this has brought on Neuropathy which affects the nerves therefore causing sensation loss.
Hopefully all the treatment will work otherwise the outcome could be rather grim.
I am going to England on Saturdary to spend sometime with my brother.
Thinking of you all.
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Hi Bernie, how lovely to hear from you. Your neighbour appears to be having a very difficult time, I wish her all the best for a speedy recovery.
Wonderful you are going to spend time with your brother, perhaps you will be revitalized when you return and we can have more jokes. Have you ever thought of compiling a book of jokes, am sure it will be a great seller? You could title it "Jokes that got me through the Big C" or something more appropriate, I am telling ya you would hit the best seller list in no time at all.
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Hello sam52.
Thank you for your post. It looks as though we have both been successful in our quest for a DEXA scan. Congratulations on pipping me at the post! I can understand why you postponed your scan in order to help your father.
I also hope there will be some progress with the osteoporosis. I do wonder whether it is true that osteoporosis caused by hyperparathyroidism is reversible, and even if it is, there is the breast cancer treatment that comes into the equation. I am still puzzled by the fact that my consultant said my hyperparathyroidism preceded the breast cancer and that I had had it for some time. If this is true, the hyperparathyroidism had not affected my height due to osteoporosis. I started cancer treatment in 2005 and my height was 5 ft 10 ins. At the end of 2006 it was still the same and I had finished treatment. I did not pay much attention after that and it was not until 2009 that I asked the nurse at my surgery to measure my height just out of interest. She said it was 5 ft 9 ins. It was then that I went back to my consultant and started thinking about surgery for the hyperparathyroidism. She had forgotten all about the hyperparathyroidism. As you know, it was during that time that we discovered each other on bc.org. I suppose both diseases have played a role. The osteoporosis really worries me and I do not think the treatment offered, bisphosphonates helps. In fact, they seem to make the bones more brittle and prevent new bone forming. That is why I shall never take them, not to mention all the other nasty side effects of them.
I am getting most of my calcium from my diet and hope it is being absorbed. The only supplement I take is a Solgar 250 mg tablet (the indication on the bottle is that you should take four). I have a glass of enriched fresh soy milk every morning, either as it is or in oats. During the day I am now taking a bowl plain soy yoghurt enriched with calcium phosphate. These two each have 300 mg of calcium, so that gives me 600 mg. I often have Green and Blacks Organic cocoa mad with the same soy milk. That gives me another 300 mg. Every day I have ten almonds and feel I should have more but think about the calories. I also have other nuts, organic black jumbo raisins, as well as fish (haddock and wild Atlantic salmon), as well as green vegetables, such as broccoli, pak choi and curly kale.
How are you doing with you calcium intake?
I saw my GP yesterday because I have oedema in my left foot. She tested for fluid in the lungs and around the heart and said all is clear. Tomorrow I go for the routine full blood test that I had already set up and she will have a look to see if the kidney function is OK when the results come in. I told her I would like a parathyroid hormone test for peace of mind and she said that was perfectly alright. I shall let you know how I get on. I really think PTH should be part of routine blood tests.
I do not envy you your long school day today. You will probably need some green tea and chocolate!
I have not done much in the grounds here either, as the weather has been too awful. I have not done as much walking as I normally do, and I am trying to get back into a daily routine that gives me more time. Being a director here is like having a full time job!
Thinking of you and hoping you keep well.
Love.
Sylvia xxxx
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Hello BernieEllen.
I am so glad to see you back on the thread, but do understand that you are busy and have other commitments.
I can understand that you have been busy looking after your neighbour. I have a close cousin with diabetes so I know all about the problems with foot ulcers. He has had one for nearly a year now and it will not clear up. At his foot clinic they want him to have some kind of special boot but he does not want it. I feel that he does not look after himself enough and will end up with an amputation. He has started putting honey on the ulcer and that seems to be helping, but I keep telling him that the honey should be high strength Manuka, which apparently works miracles.
It must be awful for her to have that necrotising fasciitis (flesh eating disease). I suppose she must be on very strong antibiotics. My cousin also has the neuropathy in the feet which causes no feeling in the feet. I do hope she will be alright.
Since neuropathy is one of the long term side effects of chemotherapy, do you think this is the same as the diabetic neuropathy? I have this neuropathy and my oncologist told me it would have been caused by Taxotere (docetaxel). It is not painful but just uncomfortable.
I do hope you will have an enjoyable time with your brother in England.
I hope you are well and please keep in touch.
Love.
Sylvia xxxx
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Hello Carolben.
I just wanted to let you know we are all here for you and wishing you well.
Love.
Sylvia xxxx
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Peripheral neuropathy is a common and distressing side effect of many chemotherapy drugs. It is often referred to as chemotherapy-induced peripheral neuropathy and, in addition to being painful, often impairs the ability of the extremities to function correctly. Extremity pain and malfunction can disrupt completion of daily tasks creating emotional and physical distress. Fortunately, there are many treatment options available for chemotherapy-induced peripheral neuropathy.
Extremity Protection
Some chemotherapy drugs can damage the peripheral nervous system, causing peripheral neuropathy. These drugs include paclitaxel, docetaxel, carboplatin, cisplatin, vincristine, etoposide and interferon. According to Chemocare, peripheral neuropathy includes pain, numbness, tingling, decreased sensation, burning, weakness and cramping in the hands and feet. Often these symptoms make it difficult to effectively use the hands. Peripheral neuropathy can also cause constipation. The most common treatment for peripheral neuropathy is to protect the hands and feet from further injury. Because sensation is decreased, the hands and feet may be more susceptible to injury. Socks and shoes should be worn to protect the feet. Hands should be protected with gloves during activities such as sewing or gardening. Hands and feet should be protected from extreme temperatures when washing dishes, cooking or during cold weather. Skin of hands and feet should be examined often for breaks in the skin.
Drug Therapy
OncoLink states that the most effective way to control peripheral neuropathy is with a combination of drug and non-drug therapy. One type of drug therapy available is a calcium and magnesium infusion given by intravenous route in a hospital setting. Often these infusions are given in combination with chemotherapy treatment and may decrease neuropathy pain. Gabapentin is often prescribed to treat pain associated with neuropathy. Pain medications known as opioids may be used in combination with gabapentin. Sometimes the dose of chemotherapy may be reduced or delayed as an additional option to control peripheral neuropathy pain. Providing comfort measures in addition to drug therapy can be valuable. Massaging the hands and feet, and applying lotions and creams to the affected areas may help.
Alternative Therapies
Some alternative therapies, including physical and occupational therapy, may help increase flexibility and range of motion of extremities. Stretching and massage may be incorporated with therapy to improve comfort. Assistive devices are available from therapists to help complete daily tasks. According to Chemocare, additional therapies that may be helpful include acupuncture, relaxation and nerve stimulation.
Constipation Prevention and Treatment
Chemotherapy drugs, pain medications and peripheral neuropathy can all cause constipation. It is important to prevent constipation rather than treat the condition. Eating a diet high in fiber and drinking 2 to 3L of fluids daily can help prevent constipation, according to Chemocare. Regular exercise of 20 to 30 minutes daily will help to prevent constipation. Often chemotherapy patients are prescribed daily medication plans to keep bowel movements regular. Peripheral neuropathy can be a distressing side effect during chemotherapy treatments, so it is important to consult with a doctor to create a successful treatment plan to control symptoms.
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Hello BernieEllen.
Thank you for taking the time to post the information about peripheral neuropathy. I found all the information most interesting. I am sure everyone else will find it useful. I am not sure about possible ways of treating it as when I told my oncologist about it, she said that it was definitely caused by the Taxotere (docetaxel) and that nothing could be done about it. I also asked my GP about it and she said the same, that there was nothing to treat it and no cure. In addition, I went to see a podiatrist for another matter and mentioned the peripheral neuropathy and she tested me for it by having me close my eyes while she prodded all over my feet with some kind of needle, and I felt nothing. She also told me nothing could be done about it.
I do not experience any pain, just a kind of stiffness under the soles of the feet and a feeling of hardness and yet the soles of my feet are very soft, as I take great care of them.
I am going to look into whether chemotherapy induced peripheral neuropathy causes the same problems as diabetic peripheral neuropathy.
We should all know the long term possible side effects of our chemotherapy and radiotherapy treatment, as well as the surgery. All we are really told about our treatment is that we may feel very sick and nauseous, hair loss, possible lymphoedema, and problems with our red and white blood cells, as well as extreme fatigue.
At least, on our thread, we have brought a lot of this out of the dark ages. Thank goodness for that.
I hope you have a good weekend and an enjoyable time with your brother.
Love.
Sylvia xxxx
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Hello everyone.
I do not really know where this week has gone. The days have flown by. Thank you all for your input this past week and I was very glad to hear from all the regular posters.
I am wondering what has happened to our Liv in Australia. She has been very quiet this week. I hope she is just taking a break.
I know we shall all be thinking about Carolben, Jenn-uk, Michael and Mumtobe as they all go through treatment.
I shall be posting some snippets of information later following on from snippets from What Doctors Don't Tell You. You will remember the ones about chemotherapy helping cancers to grow and Grapeseed extract being more effective than chemotherapy for advanced cancer. These were from page one of their website and found by clicking on news.
On page two, of all the information there, two that caught my eye was one about cancer screening doing more harm than good in the over 75s and broccoli and spinach helping prevent fractures and osteoporosis.
Wishing all of you a happy and relaxing weekend.
Best wishes.
Sylvia
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Hello Mumtobe,
I saw that you had started a thread about colouring your hair. It is only my opinion, but I would think that it is far too soon for you to start colouring your hair. If I were you I would wait quite a while, and think carefully about using hair dye. It is full of chemicals and some say might be a risk factor in the development of breast cancer. As always, there will be conflicting views. You might want to read the following links to help you make up your own mind. I would err on the side of caution and I really think it is too early to be dyeing your hair.
http://www.cancer.gov/cancertopics/factsheet/Risk/hair-dyes
http://www.ncbi.nlm.nih.gov/pubmed/3474457
http://www.breastcancercare.org.uk/community/forums/hair-dye-cancer-causing-or-not
http://ww5.komen.org/BreastCancer/Table24Hairdyesandbreastcancerrisk.html
As for taking vitamins, I think, in the end, it is a personal choice. I would think different oncologists would have different views. After cancer treatment the most important thing is good nutrition. Vitamins cannot replace this.
Best wishes,
Sylvia.xxx
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Sylvia and others: my hair is almost "gather-able" between my fingers in the back - - probably about 3/4" to 1" long. In the front it is NOT that long though. It has come in a lovely "slate" color (that's what my hair-stylist called it) - a bit whiter in the front than the back. I truly did NOT know the REAL color of my hair pre-chemotherapy.
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Sylvia: your inquiry about my 92% cured statistic. I "glean/calculate" that as 92% because:
1-I had 1 cm tumor with great margins - totally removed.
2-The test on the sentinel lymph node was NEGATIVE during surgery.
3-The post-surgical pathology showed a "micro-metastatic" bit in the sentinel lymph node.
4-The oncologist and surgeon discussed and affirmed there was no need to go further with other lymph node removal, and no need for radiation.
5-The oncologist reported that TN BC is generally 16-20% likely to recur. With chemotherapy, it is decreased by half . . . so, my likelihood of recurrence is 8-10%.
THUS, I choose to believe I am 92% likely to be killed by something other than BC. I realize that I could dwell on the 8% . . . and the "what-if's" . . . I CHOOSE not to do that.
My belief is that I have done all that I (and the medical profession) can do, and God is in charge of my longevity (which He was in charge of before BC).
Being positive, and living positively is a choice. I CHOOSE IT!
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Thanks Bernie for the information about peripheral neuropathy - especially as I start with Pacitaxel next Friday. A friend who had bc just before me said she kept her finger and toe nails painted black or very dark red, and also iced wet gloves and socks with an ice pad and put her feet and hands in them during the administation of Taxotere that she had. Anyone heard of that? She said she had minimum tingling in hands and feet.
Lovexxx
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Hello everyone.
There seems to be a lot of discussion going on about whether to take vitamins or not during chemotherapy. Like everything else, you will find differing views.
You may like to view the following links and make up your own minds what to do.
http://csn.cancer.org/node/209668
http://www.livestrong.com/article/495388-vitamin-usage-during-chemotherapy/
http://chemocare.com/chemotherapy/health-wellness/vitamins-and-cancer.aspx
Have a good weekend.
Sylvia
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The mechanisms of neuropathy that occurs with uncontrolled diabetes and with chemotherapy are different. If underlying neuropathy is present, there is a possibility of worsening with exposure to these agents.
REFERENCE: Fauci, Anthony S., et al. Harrison's Principles of Internal Medicine. 17th ed. United States: McGraw-Hill Professional, 2008.
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A Massage Protocol for Peripheral Neuropathy
By Rita Woods, LMT
My last article in the October 2011 issue focused on diabetic peripheral neuropathy and I want to stress the importance of reviewing that information before proceeding on to this protocol. This protocol is only successful when you have full client participation and when you understand the clinical significance and importance of this potentially devastating condition.
Under treating or failing to engage the client in their own treatment can render this protocol useless. This is a protocol that requires 100% participation and commitment from the therapist and client.
While my focus has been on diabetic peripheral neuropathy, is important to note that this protocol also works for chemotherapy-induced peripheral neuropathy (CIPN). Some chemotherapy agents cause peripheral neuropathy that is so disturbing and painful to the patient that they consider stopping their chemotherapy treatment. Because that is not a viable option, oncologists will sometimes adapt the chemotherapy treatment in hopes of lessening or preventing the neuropathy.
Let's revisit some pathophysiology of peripheral neuropathy as stated in my first article, "distal circulation is compromised and the blood vessels themselves become occluded beginning with the small capillaries. Unable to supply the surrounding tissue and nerves with nutrients and oxygen the resulting oxidative debt ... causes nerves to malfunction sending signals to the brain of pain, tingling, burning and numbness." And now let's recall one of the chief benefits of massage: increased circulation.
This peripheral neuropathy massage protocol can be painful to the client so care must be taken to work to the client's tolerance in each session. That being said, however, it's important to bear in mind that the ultimate goal is to gradually increase pressure so that eventually you are working tissue "to the bone." Naturally, this is a process. It may be that in the first few sessions all you can do is touch their feet. Remember, you're looking at a long-term relationship with the client so don't rush as the process can take months, depending on the severity of the neuropathy and the cooperation of your client.Protocol
- Begin each session by inspecting the feet. You are looking for discoloration such as bluish purple spots, redness, sores, cracks in the skin, fungus on the toenails (not uncommon in immune compromised cancer patients) dark spots (gas gangrene first appears as a tiny dark spot), cold areas or anything else that stands out as abnormal. (Toenail fungus is very contagious so do not work on that area if a fungus is present.) Be sure to look in between the toes and encourage the client to do the same every day. If they cannot reach their feet, have them place in a mirror on the floor to view their feet carefully. Experiment with light pressure while you are inspecting the feet. Chart your observations and include a 1 to 10 pain scale based on the client responses. This should take about two minutes.
- Next spend about one minute on each foot with light stroking, light pressure using your whole hand and not just the fingertips. Include plantar and dorsal surfaces and all tissue from the toes to the knee.
- Now begin some light compression, again using the whole hand. Spend about one minute on each foot lightly compressing the plantar and dorsal surfaces and all but tissue from the toes to the knee.
- Begin light stretching, to the patient's tolerance, by performing a full range of motion on every toe joint, at the base of the toes, and at the ankles. Spend about one minute on each foot.
- Next you will focus on digital kneading, to the client's tolerance, using light pressure on each toe from the distal tip to the base of the toe. Work on all toe surfaces, front, back and sides. Spend about three minutes on each foot.
- Continue the digital kneading in between the ligaments of the foot working from the toes towards the ankle, knead ball of the foot, the arch and the heel. Spend about three minutes on each foot.
- Now repeat the digital kneading of the toes and feet with the ultimate goal of massaging "to the bone." In the beginning, remember to work to the client's tolerance only. In each session, progress as deeply as you can. This process will take up the bulk of the protocol so spend at least 10 minutes on each foot. The severity of the neuropathy and whether or not the client is performing their homework massage will be directly related to how deep you can go and how quickly.
- Follow this with medium pressure effleurage for about three minutes on each extremity. Massage from the toes to the ankle, around the ankle and up to the knee.
- Next perform a sequence of effleurage, petrissage, effleurage, deep pressure from the ankle to the knee, spending about three minutes on each extremity.
- Moving back to the toes, begin a sequence of effleurage, petrissage, effleurage, digital and knuckle kneading, and deep pressure including all toes, plantar and dorsal surfaces, the ankle and the calf to the knee. Spend about three minutes on each extremity.
- Finish with whole hand stroking from the toes to the knee of all anterior and posterior surfaces. Spend about one minute on each extremity.
Daily, detailed self-care is essential in order to improve or reverse the tissue damaged caused by peripheral neuropathy. The suggested client homework is as follows: Spend 15 minutes each day on each foot. Lightly massage both feet as deeply as you can without causing pain.
Perform full range of motion exercises at your ankles. A fun way to do this is to "write out" the alphabet using your ankle joints and toes. Grasp each toe at the tip in massage and squeeze as deeply as you can without causing pain. Work the entire toe from the tip to the base on both feet.
Deeply stroke the skin of both feet moving in an upward direction toward your knee. Next squeeze and massage all of the tissue of your feet starting between the toes, include the front and back surfaces of your feet. Squeeze, press and massage the entire foot as deeply as you can without causing pain.
Stroke the skin of both feet from your toes to your knees once again moving in the direction towards the knees. Massage the calves then repeat the range of motion exercises at your ankles.
Whenever possible, throughout the day, take off your shoes and rub your feet on the floor, bend and wiggle your toes, roll a tennis ball under the sole of your bare feet, perform your range of motion exercises and massage her feet deeply.
Sixty-minute massage therapy sessions should be performed by a massage therapist once a week for the duration of the symptoms along with the client "homework" outlined above. Remember that infrequent, non-detailed therapy is ineffective and the main goal is consistent, daily, deep work.
For therapists who are also reflexologists, this protocol can be a nice addition to your service. For anyone interested in learning a detailed reflexology protocol that lends itself well to this peripheral neuropathy work, contact me about for more information. You'll find that combining these two therapies is a formula for success.
Editor's Note: For additional information, see Step-By-Step Massage Therapy Protocols for Common Conditions by Charlotte Michael Versagi with contributions by Rita D. Woods. Published by Lippincott Williams & Wilkins, 2011. To find this book and more on medical protocols, visit www.darienlourde.com.
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carol & ben
(((((Hugs))))) hope your are getting your head around this insane journey and finding your own way.
my thoughts are with you all the time and know you will find the strength to fight this and hoping that you are eating whatever you can to get some energy, if you want chocolate, eat it, whatever you want just have.have you been keeping up your yoga?
xx
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mum to be ((hugs))
finished chemo...yeahhhhhhhhhhh
now you can have that drink you have been looking forward to.
one drink is certainly not going to hurt you, it might actually do you some good.
xx
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sylvia ((((hugs))))
hello lovely lady hope you and hubby are well?
havent been posting much lately as just wanted some time out but my thoughts were always with you all.
everything is fine with me, meds are ok, new metformin i have adjusted quite well and taking full strength now. now looking around for some trials to show onc as dont want to keep taking navalbine and xeloda indefinitely. want to have some ammunition ready for when my current meds become resistant so the demon doesnt get the upper hand. hate u cancer!!!
went to beach today, very hot but just beautiful, walked for 2 hours. had heaps of block out, amazingly so many people not covered up. skin cancer in australia is rampart.
hoping and wishing you all a great weekened.
xx
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Thanks for that Sylvia.
I am meeting my onc on the 28th so I will speak to her about hair colouring. I understand that I will need to use an organic dye for now but will not do so until they tell me it's ok.
FernMF - you say TNBC is 16-20% likely to recur - is that in your case specifically or in general? If it's in general I would like to hold onto the hope that it's 80% unlikely to recur!
Liv - thank you, yes I am looking forward to that glass of red wine but am nervous about having it tbh. My best friend who I am bridesmaid for is getting married in July and I think I might wait until closer to wedding to have a drink.
Finishing chemo is a strange place to be. I am quite emotional and find myself worrying about recurrance incessantly!!
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Yes mom to be that is the Stat I was given. I do not know if that is for all tn 's. Yes thinking positive, glass half full.
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Nice to hear you again Liv - no yoga lessons for 2 weeks now, sigh, but have been doing a bit at home. Now that my teacher has gone to have her baby, there are 3 other classes to try out, plan on going to them all and seeing which ones I like.
Sylvia from what they described to me, I think it's a vascular port - the one that goes under your skin (or the skin flaps over it). They just said there will be a needle sticking out of it till the first chemo (which will be bandaged over). Then it's all covered by the skin, and I can swim with it (first question I asked!).
I've been such a wreck these last 2 weeks, and then I went swimming after work yesterday - I just flew through the water, it was so easy and felt so good, and it reminded me that my physical condition has not changed - I'm still feeling physically well - and I so badly needed to remember that!
It's helped me bring my attitude back to the positive side again, and I've been feeling much better today. Haven't even had a cry yet. Gosh it feels good to be out of that funk!
I started a course of Vitamin B complex shots and they have improved my appetite, and possibly my mental state and energy levels too - that stuff is good! Still trying to eat lots of good stuff and juicing and using the Ensure, even had some chocolate last night.
Had the last sushi meal with my sister - they told me not to eat sushi during the last chemo, I guess it applies to this one too?
Hope you all have a good weekend
Lots of love
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Hey ladies!
Do you all know that researchers are looking at Dandelion Tea as a possible step to kill cancer cells? Here is the article, and it references Memorial Sloan Ketering as being interested in it as well:
http://www.cbc.ca/news/health/story/2012/02/16/wdr-dandelion-tea-cancer-killer.html?cmp=rss
Maybe a cup every now and then can't hurt, huh?
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Hello Fern MF,
Thank you for your post. I was glad to know that your hair is growing well. It will soon be back to normal. The secret is to take good care of it and to eat well to encourage it to grow.
Thank you for all the information about percentage cure rate. I found it most interesting.I know you will take good care of yourself and will do all you can to stay healthy. Good nutrition, regular exercise, relaxation, agood night's sleep and avoidance of stress and worry will all help. Keep laughing and keep smiling.
Love,
Sylvia.xxx
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Sylvia,
I can't find your previous post. What was that thing you took for 3 years?
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