Emotional Impact 2 years out
Comments
-
What has been the greatest help to me (aside from my faith in God) has been taking various classes at a local Wellspring Center (center that provides free services to all cancer survivors and their caregivers). I enrolled in a program called Healing Journey and here we learn and practice various techniques such as meditation, controlling your thoughts, journalling, visualization and relaxation, getting in touch with our inner healer, etc. I also attend weekly Body-Mind-Spirit Connection meetings at that same center. Whenever one of those stressful panic-type thoughts hits me, I now find it so much easier to ward it off using some of the strategies I've learned.
-
I have spent the last year with waves of what I can only describe as horror. But, I manage to go long periods with no horror at all because of something sort of corny. I'm planning my wedding. I told my sister that I had to have a real wedding because somehow something so girly and sort of frivolous took my mind off of cancer. I've been engaged since 9 days before my diagnosis (now nearly 2 years) and thank God for this upcoming wedding.
Maybe other woman can find something that so takes over the mind that you are able to forget about the cancer here and there. I think it has to be something pretty big though. If you've got adult kids...force them to get pregnant and have a baby! LOL then you can decorate a nursery and take over everything. That's the only thing I can think of that might work like a wedding.
I am a little scared that once the wedding is over in February, I'll fall back into waves of horror...but I am going to remember that an exciting project took my mind off of it really well.
Also, we trinegs are lucky that most recurrances happen by year 3.5 or so...so those of us who have 2 years under our belts don't have very long to go before we have good scientific reason to be relieved. By the 5 year point, we are very likely cured. I think about that. Cured. A time that is coming up really soon when I won't have to fear. I think it will be amazing.
-
It seems like as long as we are being followed and we pay attention to our bodies we are doing all we can. I don't want to be complacent, then again I know I have to stand up for myself. These doctors are seeing so many patients it's easy to fall through the cracks. For me the longer I'm out the more I pay attention to my labs and my body. I don't know if any of us ever get over the impact cancer has made on us. Those silly aches and occasional pain here or there can really get blown up!!
I wish everyone some peace of mind for 2010. There are some good drugs coming. The PARP II inhibitors will be available in the not so distant future......there is ALWAYS hope.
-
Great topic thread...
I am beginning to think that there is something to the two-year mark. A friend of mine (a 2x stomach cancer survivor before 30) said that surviving cancer is like walking away after being in a horrific car crash, and you turn around as you walk away and take a look at what you just went through and you can't believe that you made it out. I am just now starting to understand what he meant. I am emotionally thawing out.
I am 19 months from Dx and I have progressed from seeing a psychologist while going through treatment to needing a full-blown, med-prescribin' psychiatrist. One of the first things he told me when I started seeing him 4 months ago was that I have PTSD. Gee, I thought I just had chemo brain, but apparently, memory loss and cognitive dysfunction are some of the most common symptoms of PTSD. He first put me on Effexor, but that only delayed the emotional healing I need to do because it kept me completely numb. So now, I see him weekly and I spend most of the hour crying....but despite all that sadness and anger, knowing that I am running straight toward my problems and not away from them gives me hope.
One thing that angers me most is that other people do not understand that cancer-free does not mean free from cancer. Some people I know think that since I am done with chemo that I am completely well. I can say unequivocally that I am not well. But I think the further away I walk from the car crash of my life that is breast cancer, the scars and bumps and bruises will heal, and I am hopeful that when I turn around and look at that crash, I will no longer feel as if I am waiting for the next one.
Namaste!
~Bethany
-
Bethany and other sisters
I also kept everything inside. I was way to busy getting ready for my "big" surgery that I did not have time to think about what was going to happen to me. I did not have chemo or rads (this was my 2nd DX in 23 yrs) only rads 23 yrs ago. After recovery from bi-lat and recon I was put on effexor for menopause hot flashes. Those as you say kept me kinda numb. I went off of them after 8 months because of constipation. I noticed something was changing within me. I did not feel happy anymore. I had my last surgery in Aug 09 and recovered from that, had several weeks of PT and then along comes Christmas. New Years Day I really sunk into a low. My DH had asked me weeks before if I hated him. That shows just how bad I was treating him. He pushed my buttons to the point of explosion and I finally had a long overdue meltdown. I screamed everything out of me. Not only about what cancer had taken away from me but other things that had happed during those 22 months after my bi-lat and recon. My DH cried with me. I felt instant relief. Since then I have been sleeping better and treating my DH with love. I had so much anger that had built up inside of me that I could not express love. I could not even pray anymore but I know that the Holy Spirit took over my prayers when I could not continue. God received my prayer thoughts. Things are so much better now. This is a great topic. I did not realize that a lot of women experience this. I did not realize what was happening to me. My DH is a happy man again. edited to add: I found this on the active topics and did not realize it was the triple neg forum. I am not triple negative but it does not matter because we all are survivors of this cancer beast and can experience the same feelings. Thanks sisters
-
Great post Bethany,
I have also been told that many women have PTSD after BC treatment...I think those of us who have been treated for TNBC are especially at risk due to the lack of a targeted therapy. We finish our "intensive care" (as someone earlier coined it) and then have to walk away.
I remember asking my husband "did all of that just happen?" and he said "Oh yes!" I couldn't believe that we had survived the previous 8 months of treatment.
This past fall, after reaching my 18 month anniversary, I had a f/u with my med. onc. and just cried the entire time. He said my style of coping was typical with TNBC survivors...I had focused so intensely on my treatments, appointments and recovery that I paid very little attention to my emotional health. Now I am making up time. It is so validating to hear that I am not alone....and that gradually, we will feel less sad, and the memories will become distant.
My boss and aunt are 5-year survivors of TNBC, and I look to them as my shining stars.
Kathy
-
I probably should know this, but what is TNBC?
-
Triple Negative Breast Cancer
-
EZ.....We are NOT hormone receptive.....They know what..well you might say feeds your kind of cancer.....So they give you hormone therapy to SHUT OFF the receptors. Another words DONT give a plant water and it should die.....Well WE DONT HAVE ANY IDEA WHAT FEEDS OURS....so we dont know what to SHUT OFF there is no medication to take after treatment is done....Ours tend to be more aggresive. I also believe our reocurrence is higher in the 2-3 year time......another words they tend to say IF IT COMES BACK IT WILL WITH THEN 2-3 years.....It does not seem to wait....I just know that my ONC. said she would feel better if she could get me to that 2 year mark.....guess reocurrence goes down some after that......
LOTS OF LOVE LADIES.....
If I should correct any of the above.....chime in and let me know.....that is just my perception of it....
-
There is something about the 2 year point...now I'm a bit passed it and freaking out as well. I'm at 2 years 4 months. I keep sort of counting down trying to get to 3 years with no recurrance. I think being educated can be a burden. Most recurrances happen at the 3 year mark for TN so that gets to me. Just want to make it passed this period of high alert. Also filled with guilt for not doing everything perfectly...don't exercise enough because of my lymphedema. Had some wine this week. I have done really well on the low fat diet though....mainly since being thin helps my lymphedema. May God help us all to that 3 year mark. Thank goodness the recurrance rate "drops off sharply" after that. At least we have that one blessing.
-
Hi Meggy. I will be 3 years out at the end of the year. I feel like Im holding my breath. Im scared but hopeful. doing reconstruction gave me something else to focus on for the last year but now Im finished with that part. My dr said this is my critical year. As if I didn't remember that, dang.
Teresa
-
But they say based on the Anderson MD TN study, the biggest risk of recurrence is the first yr. After 2 yrs, the risks drops slowly till the 3rd yr then thereafter the risks drops significantly. At point of 3.5 yrs, the risk goes down lower than that of ER+. He showed me this biggest TN study there is done by Anderson.
-
I found Cin 56 wrote this before. She is a long timer survivor and hope she can come by to this board and offer some insight. She is also a medical researcher.
Posted in: Connecting With Others Who Have a Similar Diagnosis + Triple Negative, Created: Jan 17, 2009 07:27 pm
Hi Michelle. I just posted this in another thread, so I am copying it and pasting it here, so I don't have to write it again.
One thing about triple negative is the tumor does tend to grow fast. It is an aggressive cancer. That being said, that is why the chemo generally works so well. The chemo is designed to kill fast growing cells. That is also why your hair comes out. They are fast growing cells. I would rather have TN than have positive receptors any day. Once we make it to the 2 year mark, chance for recurrence drops dramatically. Once we make it to the 5 year mark, we are at the same level with the positives who have taken tamoxifen for five years. After the 5 year mark, we are back in the normal population of women who have the 1in 8 chance of having breast cancer. According to the researchers, not one has seen a recurrence in TN women who have made it to the 8 year mark. So, yes, I would rather have TN over positive receptors any day. Women with positive receptors have to worry about recurrence for the rest of their lives, or until the cure finally comes. Some have been cancer free for 20 years and then have a recurrence. Don't be afraid that you got negative receptors instead of positive receptors. If we just HAD to have bc...I truly think WE got the better deal.
-
Hi Meggy, You and I were diagnosed just a few days apart and I was told the peak recurrence was 18-24 months...then drops until 3 years, still drops and at 5 years we are at the same risk as those in general pop. That is why I was very worried at 18 months. Now looking forward to the 2 1/2 year mark this summer. I am feeling better and better with each passing month.
Kathy
-
Hello All,
I am so glad I am not alone. I am two years out and I have to say this July was the worse emotionally. I got angry all the time and felt like my world was imploding. The weather seemed to trigger my memory. I couldn't even go outside without feeling anxiety of the cancer returning. The fear factor has increased as I put my eye on the three year mark a year from now. It is hard to not think every ache and pain as something.
This year will bring the arrival of two grand babies and a wedding! I need to keep my hope on their coming and on a happy celebration ahead not all this other stuff.
Thanks for listening,
Minnesota Mom
-
Minnesotamom - I just read your original post from 2009 this a.m., and when I saw that you just responded again today to it, I have to honestly say that I was so afraid to go to page 2 to see read your new post a whole year later. I breathed a great sigh of relief to see that, although your emotional pain is still raw (as is mine), that all is still well. Guess I'm just writing to let you know that your original post is echoed by me - word for word. You are not alone in your thoughts and feelings. BUT - two grandbabies coming - now that's wonderful.
Hang in there, enjoy your life and those babies. Seems some of us are able to back burner this beast after treatment, and some of us - not so much. This disease is just a damn gift that just keeps on giving, isn't it.
Wishing you all the best -
Linda
-
Hi fellow Tri-Negs, I am 12 years post treatment, 75 years old, and just fine. The GOOD thing to remember is that, for some reason, if you get to the 2-3 year point, post treatment, our recurrence rate drops like a rock.
This is a reason for joy.
Remember, about 2 years out, you are finally (well, your subconscious) is allowed to feel what you have been supressing all this time. It is Post Traumatic Stress Disorder, same as the vets. Almost all of us have some level of this and it can be helped by Anti-depressants, or just time.
You WILL get your joy of living back, it is a very hard thing to go through cancer and made harder by people looking at you as if you are crazy (family too), saying: "You are fine, why are you so squirrely?". It is not that easy for some of us, Just keep trudging along, get pills if you need them, this too will pass.
Gentle hugs, Shirlann
-
Thanks for your story Shirlann!
I am extraordinarily squirrelly these past two days (not feeling so super duper...) ACK! I have a nice case of PTSD from 20 years ago...and I must say, you should see me when a loud truck goes by...I jump or get super cranky at the noise. My hearing is more sensitive after chemo as well. Melissa Ethridge talked about that in an article, and it wasn't until then that I sorted out the source. I have ear plugs now which help a little bit
anyhoo, thanks again for your promising story and understanding.
traci
-
I'm coming up on my two year. At a year and a half out, my radiological oncologist sat me down and drew a little chart with a bell curve. At that point, he said, I was at at the crest of the wave, where half of recurrences have already occurred. His point was that from that point on, our survival odds continuously improve, and more dramatically as time goes on. By the five year mark, the risk of recurrence is near zero. I found that very helpful.
I can't say that it never gets to me. Just that it doesn't anger and terrify me the same way it did early on.
-
Shirlann! Good to hear from you! I was wondering where you were and realized that you are OUT there living..but thanks so much for popping in here now and then to give us all HOPE! I look for your posts all the time.!
I will be 17 months out in 6 days..18 months in 30 days..hah hah..how is that for keeping track...? Anyway..I too have seen that graph and know that the line is spiraling down for me and it thrills me....I just figure that each day I feel good is one more day towards my goal of at least two years..TNCB is scary...but..if we can make it 2 years..we are..well..pretty much good to go..or at least on par with the rest of the world..and that "ain't" a bad thing!
-
Hi Kathy, we are just days apart in our diagnosis...so we are now at 2 years 7 months!!!!! I find myself counting each month...and I have to tell the truth that I have been experiencing a lot of fear. My youngest is just 9 years old and his dad is out of the picture....I just have to be here for him. This period is quite hard for me. I think I need to see the graph everyone is talking about...maybe i saw another one. Also, my oncologist at my last visit said it tends to come back in the first few years (which of course I already knew) but then she said you have to celebrate each day. That freaked me out. Just freaked me out. I find it overwhelming to recognize that each day is not guaranteed...really too much for me emotionally. Now I'll go search for that graph.
Love you all.
-
Teresa, I also feel like I am holding my breath. Too bad they came out with the study that showed alchohol contributes not only to getting cancer but to recurrance. Wish I could just drown my worries in some wine for the next 12 months but I won't. Maybe an anti-depressant...do we know if they are safe for us?
-
I'm finding 2 years, 8 months to be a tough time. I should be celebrating but I just feel so fearful.
-
I just discovered this post so I hope you all are doing very well (from the original post a year ago). This week is my 2 year anniversary. Not only do I have triple negative BC but I also had Inflammatory Breast Cancer. A double whammy for recurrance. I saw the Oncologist this week and I'm doing real well. Still waiting to hear on the blood work sent off. My chemo sharted Oct 1st, 2008, just 2 weeks after diagnosis because of the IBC. I was to have 8 rounds of chemo (4 AC and 4 Taxol) but the Taxol caused severe Neuropathy (hands and feet numbness and pain) so I was not given the last Taxol. I had a bilateral mastectomy on Jan 29, 2009, then Feb 25 started my 33 radiation treatments. Also during radiation I was on Xeloda, a chemo pill, due to having 4 out of 15 lymph nodes with cancer cells. One year exactly after my surgery (Jan 29, 2010) I had chest pains and shortness of breath. I had to have Angioplasty and Stent because my LAD was 95% blocked. Cardiologist says was due to radiation. Then exactly 1 year from end of radiation (April 15, 2010) I developed Lymphedema. So now, I fear these anniversary's this year. I don't know if I have PTSD, but I am getting real antsy this week. So I'm glad I'm not alone. Maybe it is just this 2 year anniversary and I'll start being my old self after I get the call from the Oncologist to say the blood work was good. I'll let you all know.
Johanna
-
I understand your feelings, but I do have some hope. .........
Romans 15:13
"May the God of Hope fill you with all joy and peace as you trust in him, so that you may overflow with hope by the power of the Holy Spirit."I found that having breast cancer made me face the fact that I was going to die one day. Not something we like to think about, admit or even discuss with too many people, let alone myself! But, that is the truth. I had to make a conscience decision to deal with that fact. Wrapped up within that is the reality that my future is uncertain, whether I admit it or not. But, so is everyone else's. This is where a relationship with Christ changed my focus. If I am truly his as evidenced by how I live my life and my confession of faith, then Christ lives in me by his Spirit. That means where ever I go, what ever I face I am never alone. He is with me. I asked God to heal me of my cancer, but he chose not to. I remember thinking, o.k. that means I have to walk through this. Not what I wanted to hear, but never the less true. I began reading the scriptures with more intensity, praying more specifically and trusting him in a way I never had needed to before. I was also more humble and grateful because I saw his hand and felt his presence very deeply. That happens when we are in need and come humbly before a compassionate God and ask for his help. I don't have all the answers, but I do know that a relationship with Christ makes all the difference when we walk through the 'Valley of the shadow of death.' My continued prayer is that others experience the peace and comfort that can only come through a relationship with Christ. I can't imagine having gone through this without the help of his presence. I learned valuable lessons about myself and about how really simple life can be. I am going to die one day, yes, to be sure. But, I know that when I die, at that instant, I will be in heaven. No more pain, no more disease, no more sadness, no more fear. Until then, I continue to walk with an eternal purpose in my heart that makes everything else seem pale in comparision. God is love and he has a good plan in mind for each of us. Sometimes suffering helps us understand that plan and God's character in a way that we never could before.
I believe God wants to use each of us to accomplish things much bigger than ourselves. It is only as we seek him that we find that plan!
God bless you,
Gina
-
II'm not 2 years out..yet..18 months next Saturday...but I'm in funk..I have a hard time really caring about things...sometimes I just feel like sitting and staring at the wall...I can't focus...to all my family and friends I'm done..it is in the past..but IT'S NOT!....Everyone time I bring "it" up my family/friends go into a zone...I still need to talk about "IT...I'm a totally changed person from 18 months ago! I don't want to take any drugs..but maybe I need to...I don't know..fall used to be my favorite time of the year..now I feel like a zombie sometimes!
-
HI!!
I HAVE HAD BRC TWICE 16 YEARS INBETWEEN!!!!!WOW NO DON'T GET SCARED!!!!!!!!!!!!!!
LET ME TELL YOU IT NEVER GOES AWAY.... IT HANGS IN THE CLOSET LIKE A HALLOWEEN COSTUM BUT YOU HAVE TO TAKE EACH DAY AS IT COMES EVERY DAY IS A GIFT!!!!!EVERY SINGLE DAY!!!)))) SO BE THANKFUL EVERY SINGLE DAY.
AND DON'T GET SCARED GET MAD!!! FIGHT IT.
GET YOURSELF PRAYED OVER BY A GOOD FAITHFULL GROUP I DON'T CARE IF ITS CHRISTAN, JEWISH, MUSLIM, USE THE POWER OF GOD TO HEAL YOU MIND YOUR MIND HAS TO GET YOU THROUGH AND TRUST HIM FULLY.
I AM TWO YEARS OUT OF MY SECOND BRC IT WAS A TOTALY DIFFERENT KIND THEN I HAD BEFORE. THIS TIME I HAD A DOUBLE MASTECTOMY TOOK CHEMO AGAIN YUCK!!! AND I AM NOW ON ARIMIDEX I HAVE DONE EVERYTHING I CAN DO NOW IT'S UP TO GOD.
EVERY DAY FROM FEB 1993 TO NOW HAS BEEN A GIFT AND HE HAS TAKEN SUCH GOOD CARE OF ME!!!!!!! I WAS DIVORCED AFTER THE FIRST TIME AND BETWEEN MY CHILDREN AND MY GOD I MADE IT THROUGH AGAIN.
I DON'T EVER WANT TO DO IT AGAIN BUT IT IS NOT MY CALL. IF YOU LET FEAR TAKE OVER IT WILL YEAH IT'S SCARRY BUT SO IS DRIVING ON THE FREEWAY, BUYING LETTUCE OR EGGS LATELY.... SO TRY REALLY HARD TO LOOK AT EACH DAY AS A NEW PRECIOUS GIFT
I HOPE I DIDN'T COME ON TO STRONG
IRISHCHILD
-
TO TITAN
WOW SO WONDERFULLY SAID PRAISE GOD FROM WHOM ALL BLESSINGS FLOW
IN MANY WAYS CANCER IS A BLESSING IT OPENS US UP TO OTHERS ONCE WE GET PAST OURSELVES!!!! BUT WE STILL CAN BE AFFARID AND AT MY WITTS END I RUN TO HIM FOR COMFORT AND I KNOW HE IS IN TOTAL CONTROL.
THANKS
-
TO GMW
WOW THANKS FOR THAT POWERFUL TESTIMONY!!1
PRAISE GOD FROM WHOM ALL BLESSINGS FLOW
-
I really wish that the onc's would be more upfront and honest about the effects of the Tamoxifen and Arimidex meds. The body aches, fatigue, dementia, and the mood swings just to name a few. It is true that not everyone experiences them, but I did and many that I have spoken to have and they are listed as possible. So why leave us hangin out there like there is something wrong with us that we are experienceing any of these. Like, "oh you must be over reacting" or "it is all in your head". WTF, I finally got a therapist from the office of my onc and she has really helped me realize that I am not alone. I am three years and she told me that even when I make the five year mark, I will still have those days. I have to accept that it will always be apart of me; just like my scars,somedays they hurt, somedays they itch and somedays they just are.
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