just plain depressed
Diagnosed july 2011... with thyroid and breast cancer.. thyroid removed aug and have to deal with regulation of thyroid hormone.. still have a few months to go on that.. been a lot of problems.. mastectomy in early sept, then expander... went through a horrible reaction to meds ion oct.. had to detox in hospital.. also anxiety had eaten me alive.. say I have ptsd because I never dealt with cancer. Well I was knocked off my normal life style of teaching school, being a gramma, gardening, and riding my beloved horse... felt helpless and out of control of my own life. Had rads and just completed last week. Am serioulsly burned and am trying to cope with the rock in my chest and the horrible feeling of my skin. Am on zoloft and klonopin and synthroid. Onc says to start tamoxifen next week. Am post menopausal and really scared about all i hear about the drug. I basically cant take anything. Living now with horrible headaches and terrible acid reflux,,,, any suggestions, comfort , advice,,,,, my family is very supportive but one has to walk in these shoes to know the real story... I have seen a therapist but I feel scripted with her... dont mean to sound like i am complaining as i have always been a active upbeat individual
Comments
-
OMG complain away!! Thats what this site is for...scream rant cry we all have been there. I am so sorry you are having a hard time. Sorry you are dealing with a double C diagnosis. None of which is easy. We all feel that loss of who we used to be and although everyones journey is different in length we all experience the same feelings of anger and sadness. Its hard to ever think you will feel joy again...but you will. It takes time. You are so early in your diagnosis give yourself time to heal the physical wounds before you tackle the emotional. Let yourself feel what you feel. I know what you mean about putting on a happy face for others. Sometimes we feel like we are such a downer to everyone around us. BUT the reality is we've been through a lot and you are right..no one understands it unless they've been through it. Thats what make BCO such a wonderful place to bond and vent.. You will discover you are not the only one with these feelings and it does make it easier to know you are not alone. It does get easier it just takes time which in the beginning you hate hearing I know. I will say as I went through treatment I felt like time stood still. I thought I would never feel better , that all the aches and pains were forever. Now its all just a distant memory. I honestly cant remember the pain nausea or fatigue. I think I flushed it from my memory. You will be the same way...and when you are done and feeling better you will be so proud of the strength you never knew you had. Losing control of life is absolutely horrible...but in time things will get back on track...we are forever changed by this experience but down deep we are still the same person. Maybe with more appreciation for life...less tolerence for bad friends or ignorant people...but in time you will be back to riding your horses and loving your family. Just take this time to be selfish and give your body the rest and healing time it needs. You have been through so much trauma. I would also ask your BS or Onc for an antiaxiety. Ativan is a BC gals best friend. I took it at night to help me sleep and still take a pill every now and again when I have a mammo or MRI since I get so nervous during those times. Also, talk to your PS about what you can do for your skin to help it heal and ease the pain. I did not do rads so I have no advice to offer in that area.
I also wanna say I have been on Tamoxifen for one and a half years...nothing! Not one side effect. In the beginning maybe some bloating and crampy pains but like so many I was scared to death of the side effects. I sat down with my Oncologist and he went over a study of Tamoxifen and its side effects and stated how very rare the most severe side effects are. Then he went on to say...if the side effects are horrible...you can stop it...switch to another drug if you are post menopausal. I think you will find all your fears put to rest when you start taking it. Oh I also have irregular periods...thats it. Really has been uneventful. I am sure you will do just fine on it.
I post often on the Great Sayings about Depression thread and there was a good post about the process of grieving the loss of a breast. It was somewhere in the beginning of December if you wanna look back for it. it was very insightful. I wish docs would just tell you up front it may take a year or two for your body to feel good again. I also did acupuncture following chemo which was a Godsent for relieving my joint pain and helping me relax and sleep without meds.
Hang in there...PM me anytime if you have questions. Nothing is off limits.
Wishing you a peaceful evening
Diane
-
thank you diane. you are a godsend
-
It is normal, normal, normal to feel depressed! When I was diagnosed 19 years ago, I had never experienced any particularly traumatic adversity in my life and I basically curled up into a little ball for about two years. But the anxiety and depression eventually subsided and I lived a normal life, ultimately free from the fear of recurrence. Unfortunately, I was diagnosed with a new bc last month - but my prognosis is great and I am feeling what I consider to be normal ups and downs. I firmly believe in medication and talk therapy together to relieve depression when needed, as well as support groups - just being with other women going through a similar experience is such a relief. Best of luck to you and keep visiting here. At my first diagnosis, the Internet as we know it today did not exist and I did not have the kind of support available today. We are here for you - there is always someone here to talk to. xxx ooo
-
sdmeyer- What you are going through is awful, no fair, rotten miserable terrible.... You deserve to be unhappy. Your life has changed and not for the best.... Let yourself be miserable for awhile.... I have also had no problems on Tamoxifen. Acid reflux has always been a problem of mine and got much worse thanks to chemo. I can actually get a migraine from my acid reflux. I am now on some prescription pills that work wonderfully. They are called dexelant. I am close to two years post dx and am finally no longer seized with panic at the thought of cancer.
-
Dear sdmeyer, what you are feeling is so very normal, you have a right to feel like your life has been torn about because it has. You are so far away from being a normal school teacher and grandma, it is almost impossible to put on a happy face. Give yourself time to grieve, cry, rant and rave - your life as you knew it is so far away. Keep coming to these boards to be with women who have walked in your shoes. It takes time to start feeling like you again. I am 2 years out and that first 6 mos. is all a blur. I see a counselor and take anti-depressants, klonipin and levoxthyroxin for hypothyroid. Make sure that you are tested for thyroid levels, they should be in the 2 range, if your anxiety is still too much to deal with, ask for more klonopin or a switch to xanax or ativan. I find the klonopin works well for me and I am beginning to lower my dosage of it, along with my doctor. I used to measure my progress by the number of kleenex I left behind after an hour session. One time we walked, talked and I cried for the whole hour. The more you talk about it the better, the feelings and fears you have have to be talked to death so they start to loosen their hold on you. I was extremely lucky in my choice of counselors, he started learning about cancer and PTSD, any information I had, I made a copy for him. Now we chat, remember 2 years down the road. In the beginning I saw him once a week, and if I got too sad or scared in between I called his emergency cell and we would talk for 15-20 min., till I calmed down. When I joined BCO, I was lucky enough to find two mentors who had been down this horrible road, I PM'd them with their permission and practically lived on different threads throughout the day, talking to them. I studied the active threads and would join in if I had something to offer, just like tonight when I found you. Feel free to PM me if you think it may help, there is a burn cream called Silver-dine (something like that) that is very effective in dealing with the burns of rads. Right now you are in the throes of active treatment and no matter where you turn bc is staring you in the face, I still take a roundabout drive to avoid having to drive by the radiation oncology building. In a while the appts. will start leveling out and the time between appts. will lengthen and you will have talked about all the feelings bottled up inside you. My counselor also made me a tape of his voice leading me through a progressive relaxation tape and I used that too. I am also on an AI and have aches in my knees, but that's the only side effect. If the Tamox. doesn't work or has too many side effects you can try something else or just take a break from it. This site was a haven for me, still is, I have met some wonderful people, 8 of us live in an hours distance of each other and we meet each month for lunch and talk, they are some of the greatest women I know. It will get better, it just takes time and distractions to keep your mind occupied. You have found a great support team, use it as much as you need. Sending hugs your way, Karen
-
Dear sdmeyer, what you are feeling is so very normal, you have a right to feel like your life has been torn about because it has. You are so far away from being a normal school teacher and grandma, it is almost impossible to put on a happy face. Give yourself time to grieve, cry, rant and rave - your life as you knew it is so far away. Keep coming to these boards to be with women who have walked in your shoes. It takes time to start feeling like you again. I am 2 years out and that first 6 mos. is all a blur. I see a counselor and take anti-depressants, klonipin and levoxthyroxin for hypothyroid. Make sure that you are tested for thyroid levels, they should be in the 2 range, if your anxiety is still too much to deal with, ask for more klonopin or a switch to xanax or ativan. I find the klonopin works well for me and I am beginning to lower my dosage of it, along with my doctor. I used to measure my progress by the number of kleenex I left behind after an hour session. One time we walked, talked and I cried for the whole hour. The more you talk about it the better, the feelings and fears you have have to be talked to death so they start to loosen their hold on you. I was extremely lucky in my choice of counselors, he started learning about cancer and PTSD, any information I had, I made a copy for him. Now we chat, remember 2 years down the road. In the beginning I saw him once a week, and if I got too sad or scared in between I called his emergency cell and we would talk for 15-20 min., till I calmed down. When I joined BCO, I was lucky enough to find two mentors who had been down this horrible road, I PM'd them with their permission and practically lived on different threads throughout the day, talking to them. I studied the active threads and would join in if I had something to offer, just like tonight when I found you. Feel free to PM me if you think it may help, there is a burn cream called Silver-dine (something like that) that is very effective in dealing with the burns of rads. Right now you are in the throes of active treatment and no matter where you turn bc is staring you in the face, I still take a roundabout drive to avoid having to drive by the radiation oncology building. In a while the appts. will start leveling out and the time between appts. will lengthen and you will have talked about all the feelings bottled up inside you. My counselor also made me a tape of his voice leading me through a progressive relaxation tape and I used that too. I am also on an AI and have aches in my knees, but that's the only side effect. If the Tamox. doesn't work or has too many side effects you can try something else or just take a break from it. This site was a haven for me, still is, I have met some wonderful people, 8 of us live in an hours distance of each other and we meet each month for lunch and talk, they are some of the greatest women I know. It will get better, it just takes time and distractions to keep your mind occupied. You have found a great support team, use it as much as you need. Sending hugs your way, Karen
-
You're totally right...they don't get it. You need to surround yourself with people who have traveled roads like yours and ... sure enough...we get depressed, suffer with pain everyday, keep our thoughts and worries hidden. But we get through it. You're in a tough spot right now...that radiation is a bitch!! I was "Kentuck Fried Chris" for a long time (busted, bleeding skin with a nice milk chocolate BURN).
Be easy on yourself. You're body and mind have been poisened. Your every nerve tested. Remember...one step at a time. That's all you have to do.
-
thank you so much for all your comments. My husband has been wonderful but there are times I feel so guilty for what he has had to go through with me. Our marrige is solid and we will make it through this. I have never had an experience with so much trauma as I have with this cancer. My thyroid levels are still at 14 but have come down from 24. It take time to get those those hormones regulated. I am also angry at my husband at times because he is normal and I feel broken, I rant and then feel so bad and end up crying with him about how I feel. He is trying so hard but sometines says he can just be there for me. Never in my life would I have thought something would almost destroy me mentally as well as physically as this disease. During 2005 my daughter was diagnosed with anorexia and just stopped eating. I did all I could to try to save her and she basicslly shriveled to nothing but a skeleton, During this time I had none of the feeling that I have experienced with this cancer. As her heart started failing, etc,, I finally had to send her away for 8 months to arizona remuda ranch and saw her twice. Again I was as strong as an ox unlike now. It took 4 years to conquer her disease and she did survive. She is doing well now and off on her own... Again, I almost lost her and would have never made it if I did but this disease has brought me down to what I call the depths of hell. I cannot understand how I cannot be as strong as I was then. I miss me and cant find me. I am also so tired of hearing how strong you are from my peers. ... I just want to scream at them that I am not that strong today and feel just awful inside. My only place of peace right now is sitting with my horse while she is in her stall having her feed. She just looks at me with those big brown eyes and seems to understand. If I could sleep in that stall with her I probably would
-
Dear sdmeyers, I understand that feeling of where am I in all this, where did the strong me go, I was a rock for all the troubles in my life, then all of a sudden I was this puddle of tears and guilt and weakness. Find your moments of peace with your horse, for all the other things, all you have to do is show up. I do recommend finding a therapist and examining the possibility of medication to help with that terrible feeling of anxiety and depression. Talk therapy or crying hour with an impartial ear is essential to me. Just to have someone else to talk, talk, talk to. Sending gentle hugs to you and your horse for comforting you. Karen
-
Which thyroid levels are 14? TSH? Free T4?
I think that the main problem is that, honestly. As a 9 years Graves Disease patient, I can tell you that the thyroid hormone (or lack thereof) can play a huge number on the depression side. Did they take the whole thyroid out or just the nodules with tumor?
I think one your thyroid levels are in the normal range, most of these depression and anxiety symptoms are going to go away. I know I had an episode one time, after the radioactive iodine ablation, when I simply was afraid to start my car - I could see in my mind the car exploding when I would turn the contact on. I called my neighbor to start the car for me and after that I drove it without problems. And trust me, I am a totally normal person and never took anti-depressants or anti-anxiety (actually that is not true, lol I am terrified of flying and always take anti-anxiety while I'm flying).
But, anyway, as I was saying, try to worry less (I know, easier said than done) and be aware of the fact that it will take a little bit to get your dosage right and after that you will feel much, much better.
Also, about the tamoxifen - you said you are post-menopausal. Why don't you ask your dr. why can't you take an aromatase inhibitor? That is what is usually prescribed for post-menopausal patients.
*big hugs*
-
sdmeyers...your daughter went to her own depth of hell. Now it is your turn. Two things. One: be sure your daughter handles this well. Watch that she does not backslide in her recovery. Two: IF she is strong and healthy, she may be your best ally and source of support. As an adult, she can be there for you.
-
sdmeyers, you can count on support and understanding here. To read more about depression and how to help manage it, this section on the main Breastcancer.org site may be helpful to you.
We wish you well.
Judith and the Mods
-
I was also diagnosed wig thyca and had a thyroidectomy in Aug..it's doing havoc with my body trying to get the values under control..hope your feeling better soon
-
Thank you. My T3 t4 are normal now. TSH is a 4,6. I have been having horrible acid reflux and a terrible lump feeling in my throat. for over a month now, It getsreally bad to the point of being ill ..never throwing up.. only on klonopin and zoloft and really tired. I am really stressed and worry about the future. Can sleep but jsut feel awful Synthroid is at 137 for 1.5 months now. Radiation done and peeling buring almost gone. Please send some encouragemnent help advice
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team