Abuse Survivor Struggling With Testing

DagnyT
DagnyT Member Posts: 135
edited January 2018 in Waiting for Test Results

Hi all,

Is there anyone out there who is a sexual abuse survivor or who suffers from PTSD for other reasons who is having a bad time with the various testing procedures? I have had my issues well managed for more than 20 years through a combination of lots of therapy, meditating and EMDR. But my childhood abuse definitely involved my breasts. I have avoided mammograms, and had ultrasound and MRIs instead because it is the compression which triggers my issues. Earlier this week my ob/gyn insisted that I needed to get a mammogram after I learned that a sister had BC in her early 40s. Despite the technician and the Dr being lovely, I had informed them about my background and fears, I had a terrible reaction. I couldn’t control my shaking and ultimately threw up andpassed out. (For anyone reading this who does not have my kind of background, please know that there was no pain at all and everyone was very sweet - this is a PTSD issue for me). I have had terrible flash backs and nightmares daily since then, I can’t sleep and I haven’t been able to return to work yet. My ob/gyn perscribed me a couple of Xanax, which actually made things worse....when I took them I felt like all the awfull feelings and flashbacks were still there, but in slow motion and I felt trapped and unable to get away from them.

Unfortunately they found calcification in both breasts and now tell me I need to have multiple stereotactic biopsies. I can’t imagine how I will be able to handle those procedures. Has anyone else had problems like this or can anyone recommend some coping techniques for the PTSD?

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Comments

  • leaf
    leaf Member Posts: 8,188
    edited November 2017

    You are not alone. Mine was in 2006. I didn't pass out, though. That must have been awful! I didn't know I had early childhood abuse (including neonatal) until months later, when I got into therapy. During the wire insertion (immediately before breast excision), I did have a pain score of 9/10 (not 10/10 because I'm sure it would be worse if they were tearing off my arm). My previous biopsies were NOT as bad because the (different) radiologist was much more caring. I realize you didn't have any pain issues.

    I will have to have another wire insertion in the next few weeks/months.

    Good for you to tell your providers so they can be prepared. Know that no matter what, you have the option of walking out of there. At least that gives you some sort of sense of control. I was told before the wire insertion that I have to 'promise not to move a muscle'. Of course, I didn't know what was coming. If I would have told them my distress I would have cried, and if I cried I would have moved. At the time I couldn't verbalize anything.

    A friend of a friend (who I don't know, hence I don't know if she had a history of abuse) called the wire insertion 'barbaric', and I will use that descriptor if I do have to walk out. I don't know if they have better pain control now. Since it was immediately pre-surgical, and they didn't have an RN who could monitor, I couldn't have any oral or IV pain relievers.

    Since I got to a pretty non-verbal state of withdrawal, next time I will bring a bell or shaker along, and if they hear that, they should know I'm in distress. I will also lather up my breast with a bunch of topical lidocaine. (I know you didn't have any pain issues.)

    If you are still in therapy, you may also consider asking your therapist how best to handle.

    It doesn't matter what anyone else's experience is, if you are 1 out of 1 thousand or 1 million people who has this severe of a reaction. (That's the way I felt.) It only matters that your experience is valid! I'm not talking about pain AFTER the procedure (which was handled quite well with ice packs); I'm not talking about addiction. I'm talking about pain/distress DURING the procedure.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Hi Leaf. Thank you for your kind words. I got triggered just by my screening mammogram unfortunately. That’s why I wanted to say to others reading this that there was no pain and that my technicians were kind and caring. I don’t want my unusual PTSD reaction to just the mammogram compression to make any other woman afraid of or avoid basic mammograms.

    For the upcoming stereotactic procedures I am terrified about the length of time I will need to be compressed and still. My entire body shakes when I have a flashback and I cannot control it. I asked whether I could be knocked out, but was told that wasn’t possible because I need to “participate” in the test? Other than being able to get myself up on the table (my test will be prone not sitting), is there anything else that others can think of that I might need to do myself? Any feedback on how long the breast is compressed would also be appreciated.

    Thank you all

  • Lula73
    Lula73 Member Posts: 1,824
    edited November 2017

    so sorry you’re having to work through all this again. Is it possible to do the biopsy mri guided vs mammo guided? MRI (at least for me) had far less compression and at least you’re already laying down if you do pass out. Or can they just do an excisional biopsy so you’ll be out cold and won’t be any the wiser to what’s happening? Or maybe do the biopsy using conscious or semi-conscioussedation of some sort (that usually wipes out memory of the whole thing). Just a couple thoughts...

  • Georgia1
    Georgia1 Member Posts: 1,321
    edited November 2017


    So sorry Dagny that you are dealing with this. I had an ultrasound guided biopsy and then an MRI guided biopsy as well. You do need to position your arms where they tell you to but that's about it. So if an anti-anxiety medication would help I see no harm there. Perhaps since you are lying down that will be better than standing up as Lula suggested? I don't recall the compression lasting more than five to ten minutes. But there is some pre-test stuff like an injection of pain medication and placement on the table that happens first. I was quite tense so asked the techs to make small talk with me and that helped. Sorry I can't be more helpful.

  • Lula73
    Lula73 Member Posts: 1,824
    edited November 2017

    maybe they could give you a little Ativan IV just prior to doing the biopsy...you’d likelyneed someone to drive you home though.

  • Tara17
    Tara17 Member Posts: 386
    edited November 2017

    dagny i am so sorry you are going through this. Know that the women here are here to support you . I second others who have suggested asking about an MR guided biopsy ? During MR, there is no compression , and you can lie down with your eyes shut —and with good numbing medicine you shouldnt feel the needle —so hopefully lack of compression, lack of feelign the needle will mean a lesser chance of beign triggered


    Is there anything in particular that makes you feel safe? Someone holding your hand? Or is there somehting that makes a safe space or a safe ritual that you can discuss with the nurses beforehand that could be used in the procedure room? Wishing you alll the best

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Thank you everyone for your kind words and suggestions. I checked with my Dr. this morning about the MRI option. Unfortunately because I have micro calcifications, as opposed to a palpable mass, they need the compression to find the areas...so an MRI isn't a good choice (and she says they would still need to do the compression to guide the needles even with an MRI). I tried the Xanax my Dr. prescribed me over the weekend, and that actually made my flashbacks worse...i have never tried Ativan. If anyone has tried both and has any insight on differences between the two meds, I would be grateful to hear your thoughts. As a single woman without children or any family, I'm feeling very isolated and so I really appreciate the support you are all providing to me!

  • NancyHB
    NancyHB Member Posts: 1,512
    edited November 2017

    Dagny, I can only imagine how difficult this must be for you, and am impressed by your strength and courage moving forward. These tests can be challenging even for those of us without similar history or experiences; your bravery and determination are inspiring. I have severe claustrophobia, but must have MRIs from time to time which requires an hour or so with most of my body in a little tiny tube, often with my head in a cage. It was so difficult the first time around that I vowed never again. I'd used Xanax and never felt it helpful at all. The next time my doctor gave me two Ativan, and it made a world of difference. I felt relaxed and in control; it allowed me to process the experience and use my calming techniques (deep yoga breathing, closed eyes, self talk), and I made it through just fine. I've had 3 MRIs now and actually don't mind them at all (I fell asleep during my last one). I take one pill an hour before, and the other pill half an hour before, and I do need someone to drive me home. It would be worth at least trying the Ativan, hopefully it'll help more than the Xanax. Good luck!

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Thank you Nancy. I have seen Ativan mentioned several times on different threads. I will ask my Dr about trying that instead. I also do yoga and meditate most days and I had been planning on trying deep focused breathing as well. But I thought I read somewhere on the boards that you are actually NOT supposed to do any deep breathing during a stereotactic biopsy because you have to stay completely still? Does anyone know about that?

    I appreciate all the patience and helpful wishes and suggestions from all of you!

  • Kicks
    Kicks Member Posts: 4,131
    edited November 2017

    DagnyT -

    My suggestion would be to contact your Counselor, Therapist or Dr who knows your issues and has been helping you in the past and may be able to help you with ways of coping now. Or meds that might assist you now or ones that would be counter-productive for you.

    Unfortunately, PTSD is still not well understood within the medical world yet or by most people who do not deal with it (or have loved ones who do). No, I am not any kind of what could be called an 'expert' in any way but have gained a bit of knowledge on PTSD over the years.

    My Hubby is PTSD - has nothing to do with his 20 yrs Navy but to what he experienced when he was 9 yrs old and his Mother died. The last time he saw her alive was on Christmas Day when she was taken to the hospital via ambulance. - he never saw her again and his Father never told him anything - he found out that she had died from his school teacher the day after she died.

    I have several women friends who deal with PTSD also and some whose Hubby's deal with it. We used to have weekend Retreat here for those who are Veterans or spouse of Veterans to deal with PTSD (I fall in both groups) and I was fortunate to be able to go to more than 20 of them so learned a lot. Unfortunately, the Retreats are not done anymore.

    I have no DX but have been told by my Dr that I probably but I learned how to handle the issues a long time ago - I can not get on a 'big boat' (think ocean liner/cruise ship/aircraft carrier size - small boats are fine) even when tied to the pier because it will sink and I will be trapped in it. Goes back to issues that happened on am ocean liner when I was 6. So easy to handle - just never get on a 'big boat' again- that's easy to do as I will never have to.

    Please contact your 'people' or if they aren't available find 'someone' who is really knowledgeable about PTSD.

  • Lula73
    Lula73 Member Posts: 1,824
    edited November 2017

    the radiologist and nurse just kept me talking during the stereotactic biopsy. Yes hold still and “belly breathe” like you do when you’re sleeping. Your chest doesn’t swell out, your tummy does. Ativan and Xanax are quite different. Xanax is calming and mellow. I can see how if you’re calmed and mellow vs on guard how those internal defenses you’ve built up can weaken or come down enough that it all comes rushing back like you had happen. Ativan is more sedating to the point you just don’t care what’s going on and memory of what’s going on is often not there or you can just isolate a little piece of memory here and there. Example: I just had Ativan a couple weeks ago to put an IV line in my jugular vein while i was an inpatient at the hospital. I remember the nurse pushing it into the existing line I had in my wrist, asking what they would prep the area with (alcohol/betadine/etc), and I remember my mom coming in the room in the middle of it all and freaking out a little (she’s a nurse and she was out when they decided that this was what they needed to do so she had no idea til she walked in and the bed was way elevated and in the same position they use when they are performing CPR/using the paddles to shock your heart and she thought I’d gone into cardiac arrest-nearly gave her a heart attack!) that’s all i remember of the procedure and i don’t recall much of anything that occurred the rest of that night. At least that’s my experience with both drugs.

  • MTwoman
    MTwoman Member Posts: 2,704
    edited November 2017

    Dagny, I agree with Kicks. I would reach out to a therapist that knows you. Maybe some more EMDR? Someone who knows you and who can be of immediate help to you. Ask the facility about music. You may be able to wear ear buds and focus on soothing music.

    I am so very sorry that you're going through this re-triggering of your PTSD while you're trying to get your breast health investigated. You can do this. Activate your support system. Sending you warm thoughts and positive energy.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Thank you Kicks and Lula. It sounds like Ativan may be a good alternative for me. Unfortunately (or really, fortunately) after being in therapy for about 10 years, I felt I had worked through my issues and was feeling very good about my life. It's been 15+ years since I "graduated" from therapy and I haven't had anything bring up PTSD issues since then. So I haven't been in contact with my old therapist in 15 years.....I'm trying to find someone new now. I am scheduled for multiple biopsies on the Tuesday after Thanksgiving....they are moving me through quickly (which is both comforting and terrifying). Hopefully I can find someone to help before then.

    Best wishes to all of you out there. I know we are all scared and anxious.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Thank you too MTWoman. I see you post a lot and it really helps us newbies to hear from people who have made it through all of this crap!

  • MTwoman
    MTwoman Member Posts: 2,704
    edited November 2017

    Dagny, I am also a therapist, and I would make a serious effort to see any one of my clients who needed to be seen urgently after 15 years. You now best, but if you work with someone "known" then you'd skip past the 'get to know you' phase and get right down to business. In fact, when I was diagnosed, I reconnected with a therapist that I hadn't seen in years. But you know yourself best. If you feel starting with someone new would be more helpful, then do it. I wish you nothing but good things, including an uneventful biopsy and b9 results!!

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Thanks MTWoman. It's been so long that my prior therapist has retired (and I think relocated). So I'm having trouble trying to track her down. I agree with you, I would 100% prefer to see someone I already have a trusting relationship with and who knows my history. But I'm trying hard to find her! Thanks for the kind words (knowing your line of work explains a lot about your really helpful advice!)

  • MTwoman
    MTwoman Member Posts: 2,704
    edited November 2017

    I am so sorry Dagny, that makes sense that it's hard to find someone who retired. In my state, you can locate someone through the state licensing agency, but not sure about how that works in other states.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    hi all, wanted to post an update. I see that there are a lot of “views” of this thread, which makes me think there are possibly some other survivors on the board who feel more comfortable reading than posting...so here’s where I am. I’m going to do two posts, so each won’t be so long.....

    Improvements-

    • I changed the dr who will be doing my biopsies (is there an abbreviation for that kind of doc on the boards?) My original dr and her staff were lovely and gentle with me, but having had such an overwhelming experience last week, I felt that just seeing her again was going to contribute to my stress level.
    • My new dr is actually the wife of an old work colleague. So although I had to get over the uncomfortable decision to expose this very painful, and private, part of my past to someone who indirectly knows me, it was a good decision. First, I feel like I will feel a little bit of “good” pressure to try and keep myself together. But at the same time, I feel like I am a real person to her, not just a number, and so if I fall apart I am not as worried about feeling judged or blamed.
    • My new dr set up a time to talk with me on the phone, for about 30 min. I told her about my PTSD and the awful experience I had last week. We talked about exactly what things were my trigger (the compression) and my reactions (flashbacks and uncontrollable shaking). She explained why this particular biopsy procedure is the only one that works for my situation.
    • My new dr is a woman and all of the techs and members of her team that I will interact with will be women and I gave her permission to tell all of them about my abuse background.
    • My new dr has had this very same procedure herself! So she has been on both side of the needle and that really made me feel more comfortable.
    • We agreed in advance that if I say stop, she will stop at any point in the procedure. And she reassured me that she would not be upset at me if I have to stop.
    • I need multiple places biopsied on both breastsand she is going to start with the areas that look the most concerning, so that if I feel I can’t do more than one site at a time and ask her to stop, then she’ll have the most important samples.
    • She should have test results on the Friday after my procedure, so there is a good chance I won’t have to wait through the weekend.
  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    ok, here is part 2 of my update post...the things that are not going so well (trying to keep things very honest here):

    • At 50, I have only been getting my period every 3 or 4 months and I have always experienced a high level of breast tenderness for 8-10 days beforehand. So, of course, I just started PMS symptoms this morning which will mean that my biopsies will happen right at the worst part of my regular pain! I don’t want to reschedule, because like everyone here knows, the waiting is too hard.

    • My new dr has asked me to come in for a visit the day before my procedure. She was upfront that one of my locations, directly behind my R nipple, is very challenging and she wants to look at my breast in advance and try to see what the best way in will be. She was also honest with me that biopsies in that area are often painful. Because the numbing shots themselves really hurt in that area, many patients find that the pain of the procedure versus the pain of more numbing shots is about the same and they opt to power through rather than get more numbing shots. She did reassure me that we could stop and she would give me as much numbing agent as I wanted....but this is definitely stressful info.
    • I also happened to mention to her, when explaining that I was starting PMS symptoms, that I was having extreme itching and scaly skin on my R nipple and areola. She was concerned about that and when I see her on Monday she wants to look at it and says she will probably recommend even more biopsies to rule out Pagets. (And of course, like so many of you, I have complained about this problem for a couple of years to my ob/gyn who dismissed it and told me to moisturize.....)
    • My new dr recommends that I get some prescription pain medication due to the combo of my PMS and the amount of tissue she is planning on taking out if I can get through all the sites. Plus she highly recommends I get some ativan. I asked her about the EMLA cream that I have read about on the boards, and she said it was fine to get and use it. She said that she has had patients who found it helpful, but others who didn’t. Of course EMLA is not over the counter...
    • I have not been able to track down my old psychiatrist, it seems she both retired and moved out of state. Because I need medication, I can’t go to a therapist. Despite multiple calls to various drs, I have not been able to find a single psychiatrist that can see me before next week (in fact no one could see me before January!)
    • My ob/gyn says she isn’t comfortable prescribing meds for me because I didn’t get any symptom relief from the Xanax and with my complicated background she doesn’t know what is appropriate. She did say she would see if she could pull some strings and get me an appt with someone...
    • So, my backup plan at this point it to simply have a meltdown and take myself to the local ER and pray that I get a kind ER doc or PA who will realize that what I am looking for is only a couple of doses of Ativan and pain pills and anesthetic cream....not someone looking to scam prescription drugs or get high. I plan to bring my radiology report and the paperwork for my upcoming biopsy so they can see I’m genuine.

    So....as long as I can find a way to get some meds, I think there are more improvements than negatives.

    I hope that everyone can enjoy a quiet and happy Thanksgiving, whatever that means to each of you.

  • Georgia1
    Georgia1 Member Posts: 1,321
    edited November 2017

    Thank you so much for taking the time to update us. Sounds like you have a solid plan and we will be sending good thoughts your way.

  • Lula73
    Lula73 Member Posts: 1,824
    edited November 2017

    can the new dr write you the prescriptions you need? If not, I’d ask if she could help get you in to someone else who will. With her helping get you in with someone she will likely talk with them directly and couch for your intent. It’s a crap shoot at the ER especially with so many pain pill seeking individuals that flock in. In the meantime, I’d find a new OB/GYN-that reasoning she gave on not prescribing you something different than xanax because of your reaction to it is BS. If someone has a reaction to thebirth control pills/estrogen cream/antibiotic she prescribed would she tell them sorry you’re out of luck? No. She would write a new prescription for a different kind.

  • Polly413
    Polly413 Member Posts: 124
    edited November 2017

    I am deaf for human speech and lip read. When I had my sterotachic biopsy, which was done by the breast surgeon, my husband was allowed to be in the room with a protective vest except when the radiation was actively ongoing. At those points he stepped behind a shield. His role was to tell me the instructions of the surgeon who was sitting below me where I could not see her. Since he is easy for me to lip read this was a tremendous help in a practical way but it also was very reassuring to me to see his face. He was right there inches from the table on the opposite side from the surgeon. Maybe because of your unusual situation you could talk with whoever is doing your biopsy and ask if a family member/friend could be there for you.

  • MTwoman
    MTwoman Member Posts: 2,704
    edited November 2017

    Dagny, BRAVO for the plan that you have set up for yourself. I think it sounds like you've problem solved very well how to minimize the impact and have a trained support system around you.

    Having worked closely with psychiatrists for years, I do understand how difficult it is to get in and see a new one urgently. So here is another work-around option that I'll toss out there (to add to the options above), at the clinic where I worked, we frequently got calls from docs (non-psychiatrists of all types) who had patients that they wanted to be seen urgently for meds. What we did much of the time was consult. For example, the lovely and compassionate new doctor might be able to call a psychiatrist that she is acquainted with and present your case and get guidance as to what meds (Ativan etc) would be helpful for your new doc to prescribe. It would be a good idea (if she was going to do this) for her to have a list of meds you've taken both with success and ones that you had poor or no response to (as well as your previous working diagnoses etc). Please pm me if I can be of assistance in putting together helpful info to further that consult.

    Don't forget to keep breathing, nice and steady. You can do this!

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    Thank you everyone! Your support and wisdom means more to me than I can tell you. Lula, I thought i was overreacting to be annoyed at my ob/gyn's response. Thank you for validating my feelings. I did reach out to my new dr also and she said she will work hard to find me someone to help. I did ask her why she herself doesn't write scripts (neither did my first dr). She said really honestly that it is a matter of keeping her malpractice insurance premiums affordable. Apparently when you write prescriptions the cost of insurance goes up astronomically. I can understand that! Polly I will definitely ask about the option for a friend to be in the room with me....although as a single person without kids or family, I'm not sure I have someone that I'd feel comforted by. But I am going to at least find out if it is an option. MTWoman, if i am not successful in getting an apt set up by Friday for meds, I will certainly pm you.

    Thank you ladies

  • MTwoman
    MTwoman Member Posts: 2,704
    edited November 2017

    Dagny, one last thought. Your GP (or whatever doctor you have that you know the best) might be able to do the "call a psychiatrist for a consult" thing. Anyone who knows your medical history is even better.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    thanks MTW. My new dr says she thinks she can get someone to talk with me on Friday, just as you described....band-aid for the bigger issues, but someone qualified to help me get through the next week. I never thought I would be frustrated that I have been generally healthy enough over the past decade that I don’t have any doctors who know me or my background!

    I will keep folks posted. And I am sending out good wishes to everyone on these boards for the Thanksgiving holiday tomorrow

  • Kicks
    Kicks Member Posts: 4,131
    edited November 2017

    For different ones of us - different Drs do the biopsies. For me, it was the Radiologist who wanted US right after the new mammo who did the biopsies immediately. For some it is a Surgeon (or other MDs) who do them. With my BCC and SCC (Basal Cell Carcinoma and Squamous Cell Carcinoma) which are skin cancer totally unrelated to any BC, it was my Derm. PA who did them.

    Your new Dr who is doing your biopsies should be able to call in a 'script for you to pick up for EMLA (or generic form). There is an OTC form of it that was written about 'here' within the last year but I know nothing about it. If you do get EMLA (or generitic cream), remember it needs to be put on the area at least 20 mins before for it to numb the area. Also to cover it with a bit of 'saran wrap' to keep it in place and not on shirt.

    Did you ask your new Dr if the Facility she's at has a Staff Psyc Dr? The Can er Center I went to did for those needing.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    hi all, I am copying in this note that I just posted in the Pagets thread, because I see that this is a more active area. I will update folks on my meds situation in a different post (but looks like I can see someone tomorrow!)

    *********

    I have biopsies scheduled on Tuesday for calcifications on my R breast (right under / beneath the nipple area) and on L breast (around 1 o'clock up much higher). They were discovered on mamo. I have read the full Pagets thread and here is my issue-

    For the past two years I have had many of the various pagets symptoms described by everyone on the Pagets thread (other than crusting / oozing) on BOTH nipples/areolas. Since they can see a cluster of calcifications behind my R nipple and I am already going to be numbed up in that area, I am going to insist that they do a nipple biopsy on that side. But since no one on the Pagetsthread seemed to have been diagnosed with pagets on both nipples at the same time, I am struggling with whether I should be insisting on a nipple biopsy on the L breast as well. That isn't the area where the calcification cluster shows up on the L breast, so I won't be numbed already and I knowthat having it in both nipples is extra rare....but...? Fortunately (or unfortunately) my itching and scaling is present on both sides right now, so at least the dr can see it..

    Thanks for your advice.

  • DagnyT
    DagnyT Member Posts: 135
    edited November 2017

    ok guys, I just wrote a long update post and it somehow disappeared! So if two posts pop up, sorry for the repeat info.

    So the bad news, my new dr was not able to find anyone willing to see me before tomorrow, despite her best efforts. BUT, the good news, with the help of the internet and a computer programmer friend, I was able to track down my old psychiatrist from 15 years ago! She can’t write scripts anymore as she is retired. But she got in touch with the dr that took over her practice and told her exactly what she wanted prescribed for me. So, if all goes well there should be a package of meds waiting for me at CVS tonight after work! And maybe this will be all for the best, because my old dr ordered a specific PTSD med, together with Ativan and EMLA, and no dr that isn’t a PTSD specialist would have been likely to put that combo together.

    I spent the weekend mostly in bed, the PTSD was severe enough that I couldn’t sleep at all during the night from the nightmares, but was able to nap during the daylight hours. So I feel like I wasted an entire long weekend, and we had lovely weather up here on the east coast!

    But one more day to go....I meet with my new dr at 3pm today so she can mark out all the various areas that she will need to access and so I can sign all the paperwork in advance since I plan on being extremely loopy tomorrow!

    Thank you all for you continued support.

  • MTwoman
    MTwoman Member Posts: 2,704
    edited November 2017

    Way to keep pursuing an answer Dagny! I've got all crossed that your med package is waiting for you. Try to do focused breathing when you can to add to your overall benefit from the meds. I'll be thinking about you.

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