See full list of all Hormone Therapies
What Breast Cancer Survivors said about their Hormone Therapies.
Starting Tamoxifen after rads are done
Offered 5 years of Tamoxifen but declined. More interested in quality of life than quantity at my age. I had a long, rotten menopause and am not into that again thanks!
Radiation on ovary to stop ovulation. August 15-20,2012. No special side effects. A bit of hot flash as a menopause symptom.
No hormone therapy as I was triple negative.
Tamoxifen for 5 years and Aromasin for 5 years after that.
I took Tamoxifen in 1991 and am currently getting Faslodex once every six weeks since 2004.
Started tamoxifen 11.30.11. KILLER hot flashes, night sweats and sleeplessness. Started taking it in the AM rather than the PM suggested by my doc and over time flashes decreased in VOLUME and number and sleeplessness got better as well. I can usually sleep 6 hours uninterrupted now, sometimes eight. Yay me!
Tamoxifen for 5 years Lupron shots to shut down my ovaries Ovary removal in near future
Doing hormone therapy with Zometa for the bones
i am taking tamoxifen,started it 3 weeks ago,on it for 5 years,side effects at the mo,terrible hot flushes
No hormone therapy.
This will start after radiation in 2011.
Bone pain! Night sweats.
I started Arimidex in December of 2010. It makes me very tired all the time and I have a hard time focusing. It also makes my joint ache to the point where I have trouble walking. Exercise is very difficult. I'm told I have to be on it for five years. I'm not sure I can take five years of this drug.
Tamoxophin for 3 years, Femara for 6 months--hated it because every muscle or joint in my body ached. Back on Tamoxophin--though my oncologist isn't happy that I wimped out. To bad!
Arimidex-joint pain, hot flashes, mood swings
Tamoxifen started September '10 plan is to continue on it for 5yrs. Side effects are hot flushes, pushed into early menopause also I Need to talk to GP as I am having alot of joint pain mostly in my upper legs and fatigue
hot flashes, memory loss, lack of energy, depersion
What Prostate Cancer Survivors said about their Hormone Therapies.
casadex, lupron, back pain, 6 months in the beginning
The hormone ablation takes away all the wonderful things that testosterone gives you: strength, vitality, potency, hair on your body, and worst of all desire.
zoladex and casodex, little hot flashes
Leuprolide, Flutamide 2009 thru June 2010, At present taking some time off until PSA starts to increase. Last tested .05 on 02/12/2011.
Nine Lupron injections -- one every three months, ending Oct 2009. Genital shrinkage, loss of sex drive, emotional lability (mood swings), reduced mental acuity (a/k/a chemo-brain), no erections, and high-temperature hot flashes. And my constant companion: fatigue. Second round of Lupron to accompany radiation; two, three-month shots with the same wonderful side effects!
Every 90 days
Lupron Aug 2012 and continuing
Lupron shot every four months. Had some break in treatment but consistent since Sep 2011. Hot flashes, depression, need to shop, etc
Degarelix: Started 1/31/13 No major side effects. Increased appetite, slight temporary discomfort at injection site. So far drug has been excellent for me. Told by dr. that bone density thinning may be a problem in long run.
Lupron. 2 years continuous ADT (4 shots, 6 month dose)
Lupron 2/10/2014 to July 2014 Hot flashes so far.
Started 3 months ago ..usual side effects
Lupron, 8 months in 3014; extreme fatigue, loss of libido, loss of muscle mass and strength
What Lung Cancer Survivors said about their Hormone Therapies.
Arimidex - 7/15/08 to present. No side effects
What Non-Hodgkin Lymphoma Cancer Survivors said about their Hormone Therapies.
Progesterone 2 day cycles every three months 2012-2013; low dose estrogen bc pill begun February 2013
Vivelle dot 0.025mg and 100 Prometrium progestrone (chemo-induced menopause after the 4th round of chemo)
Induced Menopause to preserve as much fertility as possible = Plus side Hot flashes = not so positive
What Kidney Cancer Survivors said about their Hormone Therapies.
no treatment yet?
No hormone therapy
What Pancreas Cancer Survivors said about their Hormone Therapies.
after my hysterectomy in 02 it was suggested I take HRT but because my cancer was estrogen related I refused to do that and used Estroven for the menopausal symptoms
recieve injections every 28 days of Sandostatin LAR
What Oral Cancer Survivors said about their Hormone Therapies.
Early September until late November, used a feeding tube for 100% of food intake.
What Ovarian Cancer Survivors said about their Hormone Therapies.
Bio-identical HRT in the form of transdermal creams: includes Bi-estrogen, Progesterone, and Testosterone...started March 2007. No side effects to speak of so far! I highly recommend seeing a HRT specialist to look into bio-identical HRT. After reading "What your doctor may not tell you about menopause" I refuse to go on the "conventional" synthetic hormones most doctors prescribe.
I'll take my chances without it
I am taking Estratest and was told to go see a hormone specialist because one HRT does not fit all but Im afraid to much hormones would send me out of remission.
estrogen patch then ring, 5/06 to present: no hot flashes. no libido.
NONE DIDNT EVEN HAVE TO GO THRU MENOPAUSE BECAUSE U HAD PROBLEMS PRE MENOPAUSE DR FIGURED I WAS A BITCH ALREADY SO HE LET ME SKIP IT..LOL
Lupron Depot shots (for endometriosis, not for cancer) Oct. 2011-March 2012; migraines and mood changes were the main side effects.
I take daily pills for hormone replacement...
None to date
Venlaflexine for medically induced menopause hot flashes. It helped. I got off it cold turkey after one year. The withdrawal symptoms were bad; 3 weeks of hives, head pain, dizziness, pain in my neck and collarbone, back pain, upset stomach, nausea, dizziness, blurry vision, auditory hallucination- whizzing sounds and echoes.
Undergoing hormone replacement
They are trying to save my left ovary, so I was put on a medication that is supposed to help. I can't remember the medication name.
What Thyroid Cancer Survivors said about their Hormone Therapies.
will be on thyroid meds rest of life
Thyroid replacement therapy immediately post op
Levothyroxine... level to be altered once i finally get to see the endo after 6 months of waiting and a cancer diagnosis
Currently on Cytomel 25 mcg 2x day
Ever-increasing strengths of Synthroid. How much is too much? Lower heart rate and blood pressure.
Levothyroxine .137 mg daily plus additional half-tablet once a week. It took almost a year to get the correct dose.
Currently taking Synthyroid 175mcg daily.
Synthroid - 75mcg
Synthroid has been changed 3 times since December so I don't know what good feels like???? Can't wait to feel it though. I am still very fatigued, but have a very hard time sleeping for more than a few hours.
Ive been on a form of hormone replacement for almost 2 years, once i have my thyroid removal surgery ill be on full hormone replacement
Cytomel - Thyroid Hormones since after surgery in Sept 14th 2011. They are still low so chills, constipation, weight gain, etc.. Switched to Synthroid 150mcg (thyroxine) Jan 17th 2012
I take 150 mcg of Synthroid 6 days a week and on the 7th day I take a total of 300 mcg . My doctor has had to change my dose 4 times since my surgery. It is a very long process. When we are to low I am tired, moody, depressed and I gain weight. When it is to high I have headaches, trouble sleeping, heart palpitations and anxiety.
Thyroid hormone replacement therapy for the rest of my life.
Levothyroxine, 175mcg daily.
What Colon and Rectal Cancer Survivors said about their Hormone Therapies.
I need some believe me!!! I have severe heat surges with extreme beading of sweat on my forehead groin area and mid chest area.
Advised against hormone replacement, especially estrogen , because of my age & the chance of "feeding" any immature cells that could develop into breast cancer.
Hormones and radiation twice over last 3 years and waiting on next treatment option
What Liver Cancer Survivors said about their Hormone Therapies.
i will tell you
What Cervical Cancer Survivors said about their Hormone Therapies.
I was 37 when I went through these treatments, so after awhile I got hot flashes (which I still get) I dont like that I am losing estrogen at too young an age, it has slowed, what has been a fast metabolism all my life! I have been afraid to take any hormone therapy up to this point.
It remains to be seen.
That will come after the hysterectomy. But frankly I'm not worried for me, I'm worrying about my poor hubby, he's the one that has to deal with me! ;-)
Kept ovaries (they were moved upwards away from radiation). Menopause started in the fall of 2011. Insomnia, anxiety and depression.
H.R.T. achy bones and limbs...stiffness in the legs and hips
9 months post treatment and have begun hormone replacement therapy. Hoping to ease the menopause symptoms brought on by the radiation and chemo treatments. Hot flashes, weight fluctuations, facial hair and most other awful symptoms have started earlier than normal. Wait and see about the side effects. I am prone to breast cancer, God willing it won't become an issue :( **Update** Have thrown out the HRT as mother was diagnosed with Stage 2 Breast Cancer resulting in complete mastectomy of her right breast. Insert personal paranoia here... Her last check up and lymph node biopsy came back clear, so no radiation or chemo, but a daily pill for the next 3 years. Still riding the early menopause train...
none as of yet
What Testicular Cancer Survivors said about their Hormone Therapies.
had no treatment
What Anal Cancer Survivors said about their Hormone Therapies.
evista (raloxifene), 2/98 - 93; turbo-powered hot flashes. Tried Fosamax and prempro, could not tolerate. Switched to Boniva, then discontinued.
Arimadex 6/2014 bone and joint pain for the first few weeks.
Do guys need Testosterone? Help ... I'm shrinking, I'm shrinking.
I was put on Lupron because I could not afford to preserve my eggs, and was told that I was likely to become sterile, so the Lupron was an attempt to save my ovaries. This put me into a post-menopausal state, giving me the symptoms of someone going through menopause.
What Peritoneum, Omentum and Mesentery Cancer Survivors said about their Hormone Therapies.
no side affects
What Endometrial-Uterine Cancer Survivors said about their Hormone Therapies.
No way; I think the pill caused this in the first place! >:(
started w/tamoxifen-it caused constant unusual periods which alarmed fam-doc who did emergency biopsy to find huge tumor in uterus. After hysterectomy did arimidex for 6 weeks-side effects were mostly fatigue and bone pain,currently on aromasin. no side effects as of 9/02/10
Haven't started yet. Need advice.
Too late for that, contra indicated
No hormones, ever!!!
I am on Megestrol because of maligant cells in the pelvic washings at the time of surgery. This has me very confused!
My oncologist put me on an estrogen patch to prevent chemical menopause. I don't even notice the patch. I haven't experienced any menopause symptoms, so that's been great. I have an occasional migraine from the patch, but I've gotten migraines my entire life, so it's no different than before. I do occasionally get insomnia, but that was also something that I've dealt with my entire life, so it's not different then life was prior to the surgeries.
Megace started June '15 increased appetite very emotional weakness elevated blood sugar
What Parotid Cancer Survivors said about their Hormone Therapies.
Tamoxifen no effects arimidex. No effects
What Throat Cancer Survivors said about their Hormone Therapies.
What Hodgkins Lymphoma Cancer Survivors said about their Hormone Therapies.
Zoladex for 6 months while having ABVD. This drugs shuts down your ovaries and hopefully protects them from the chemo. This was the same as being in menopause so was not fun - hot flushes were horrible, decreased sex drive. Zoladex is not strong enough to protect the ovaries from high dose chemo and stem cell transplant so I have stopped this medication and am now on the regualar contraceptive pill. High dose chemo will likely make me infertile and possibly cause early menopause.
What Bile Duct Cancer Survivors said about their Hormone Therapies.
iam a nice girl loking for man
What Leukemia Cancer Survivors said about their Hormone Therapies.
HRT 1991 - allergic to female hormone therapy
What Uncategorized Cancer Survivors said about their Hormone Therapies.
Just taking estrogen now for really bad menapause side effects. Doing much better now that I am taking the estrogen. I've now stopped the update because although no doctor will confirm this, I believe this is what is causing my cancer to keep coming back. Odd. I get the all clear, then when restarting estrogen, 10-12 weeks later I'm told the spot is back. So I am done with estrogen.
He is also taking cortisone for replacing his hormones for his adrenal gland - the Mitotane stops the Rt gland from producing hormones.
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