- There has been so much in the media about the pregnancy of 3 sisters, 2 Kardashians and a Jenner. I am a fan of all three and now they have started joking about it (being pregnant)
- They are posting 2 or 3 lipkits blue and pink and asking fans to choose.(if they think the baby is a girl or boy) Since the media has confirmed the pregnancies all photos they have posted are conveniently not showing their bellies. It’s as if they are playing with us, their fans. As a woman that can’t have my own biological children and I also can’t adopt, I think it’s cruel to play with the gift they have been given. They have every right to keep this to themselves but, the games and showing apart of their belly isn’t cool. I look at their posts that are on my timeline and it brings me to tears. I’m disabled as you may know from previous entries and my$ is fixed and it’s not a lot. Once my bills are paid I have nothing left. I’d like to get new sheets or a throw but can’t afford it so seeing them with seemingly perfect lives and sharing everything with us makes them keeping their pregnancies secret weird to me. I can see not showing the child after it’s born but their pregnant bellies??? I really don’t even think they are pregnant and will have this opinion until they announce it. With my medical issues, it hurts to see celebrities I watch and follow be willing to share their entire lives and then not really go secret but start playing games with their possible pregnancies. It’s bad taste, IMO. I know they can’t possibly know how this could affect women like myself and I guess that is why I feel compelled to write about it. Only a handful of people will read this so it won’t go far anyway, I’m sure if it.
I hate being me, I’m fat and I’m sick. I’m alone and I’m lonely. My life is miserable and I don’t see it changing anytime soon.
There was a woman walking from a Bible study group a few homes away from my parents home maybe 6 months ago. She called out my dog by name, yet didn’t know his name, she asked my mom if she was the owner and mom told her no, that i was. She walked up to my mom and said, I pray for your daughter’s health and I see cancer and was using her hand to go in a circular motion in front of her stomach. My mom told her I didn’t have cancer but I had lupus and kidney involvement so she assumed she was referring to that. We were blown away by this woman but really didn’t think any more of the cancer until a few weeks ago when i was diagnosed. i wish i could talk to her, maybe she was an angel just meant to inform my mom of what was to come. whatever or whoever she was i am grateful for her.
It’s really been a while since I’ve written so here goes. i don’t even know where i left off but i will just begin where i am now. June 1 i had surgery, the pathology results came back verifying that i have cancer. i actually was expecting it because i had a similar growth removed and it was cancer. the difference is the location of this growth requires chemotherapy or radiation to completely get rid of the cancer. but, due to my kidney disease, chemo is risky while radiation is not. at the same time chemo is more effective and in most cases cures this type of cancer. i will see my oncologist on June 5 to go over all of this, depending on his opinion i will move forward. i may even get a second opinion at the center for cancer treatment in Atlanta. with my lupus, kidney disease, coronary artery disease, anemia, chronic pancreatitis and colon ulcers my case may be a little bit more complex than the norm. it’s scary because it’s unknown but, I’ll get thru it and honestly i see this as an extended detour that i have to take before getting back onto the main road… lol! (gotta bring laughter into the mix) my family says, you’ve been thru so much and you are so strong, i don’t really see that. i feel defeated and beaten up like an abused woman. the other day i was thinking about the fact that i have 3 medical conditions that could end my life; lupus, renal failure and cancer, it took me aback for a second and then put me in the mindset of a fighter and a survivor. i have no choice, my aunt told me a positive outlook can be the difference between surviving and not. Wait, What?!?!??????)
Moo It’s been awhile since I have been in here and I really don’t think anyone follows me, but it is therapeutic to write down what I’m going through. I didn’t look at my last post to see what it was about, so this would be a continuation. So I will just start. My kidneys have been up and down as far as function % goes and for now I’m in stage 4 renal failure. Talks of dialysis is still on the table,but thankfully I don’t need it as of now. My doctors also found tumors on my stomach called carcinoid tumors and they were malignant stage 1 cancer. The prognosis is nearly 100% in all patients so my doctor removed the three with no problem. About a month ago he went back to make sure he had gotten them all and unfortunately found two more and removed them successfully as well. I will have to have a repeat surgery in 6 months to check for recurrence. In addition to this, I pave had warts on my backside for about 3 months and I was told because my higher dose of steroids it would not heal and I just had to deal with it. Well, the steroids went down and the warts didn’t get better. I went to a dermatologist and he froze the area and was planning on doing several rounds of freezing over several months. When I returned after a month for the second freezing I told him the area was no better and it was actually worse than before the freezing. At that point he suggested that the best bet would be to just have it removed, it’s a cluster of warts. So he referred me to a colorectal surgeon to get his opinion and he advised me that th needed to be removed and tested. Unfortunately, the hospital he is affiliated with isn’t in my network for my insurance so he couldn’t do,it. He then referred me to a general surgeon and he is going to perform the surgery in about a week or so, I will finally have this issue taken care of. It’s so weird that it seems like every part of my body has something wrong with it. Lupus affects my joints and my skin, I where issues with my scalp, my ears, my hands, my feet and ankles, my stomach, my vajj, and now my butt. It sucks to hurt literally everywhere. Also on top of that I had an argument with my sister and I have learned from talking to my bible study mentor that we are sisters and the bottom line is we love each other. We will argue we will yell and we will shout but we love each other and I had forgotten about that. I will be seeing her this weekend. I’ve also been staying with my parents for awhile. This hasn’t set well with my sister but the truth is I feel more comfortable here especially when I’m sick. My mom also prefers for me to be here because she doesn’t want to have to come back and forth from her house and my house to help me. And I have company when I am at home I’m alone and I don’t even have my dog because I can’t take care of him properly. I’ve asked my mom if she’s ready for me to go or if I’ve over stayed my welcome. She says I’m her child and there is no way I could over stay anything, I’m always welcome here. I love my mom. My lupus has been ok, I think it’s pretty stable and it’s time for my re evaluation for disability and I got a call that based on the information thus far they couldn’t determine if I was still disabled. So I went to see their psychiatrist for a evaluation, I. Not sure if it helped or not but I also had my PCP do a physical so I’m hoping this will help me. If,they deny me my lawyer will step in to assist me once again. It’s scary becaus I have bought a home and all of the bills that come along with that. So I depend on my disability to keep my independence. I know with all of my heart I couldn’t hold down a job working a typical 8hr day 5days a weEk. I would need the company to make several exceptions for me during my shift and this is actually what lead me to getting fired from my last job. 15 years I gave to that place and fired because of something I can’t control. I’m sleepy people night.
Originally written on March 9, 2016
“My parents have my dog right now and his name is Reece. There is a prayer group that meets a few houses away from my moms house and she was out with Reece and a woman walked up to her and told her she felt compelled to pray with her and Reece. My mom had not told her my dogs name but, my mom very well could have called out to Reece prior to the woman approaching therefore she would know that was his name. She told my mom that for some reason she feels cervical cancer in someone, she asked if Reece was my moms dog and my mom said no he’s my daughters. The woman said I need to pray for her health. My mom told her I had lupus and a number of medical issues and they proceeded to pray. I know the cervix and kidneys are relatively in the same area of the body and I just had an appointment with my gyno and forgot to mention these painful stabbing feelings I’ve been having in my lower abdomen and lower back that I just attributed to my renal failure but, now I’m wondering could it be something else. It makes me so nervous and it’s almost impossible to wait until Monday. Since hearing this from my mom I can’t help but go to negative thoughts in my mind. I call on the Lord and tell the devil to get away from me. I also have a Healing Declaration which has several scriptures promising Gods healing. Despite this, the devil creeps in my mind and I think of not surviving this battle. I ask that you all pray for me as I continue to pray for all of you. Thank you.”
I never posted this because I felt it wasn’t something worth sharing. But, with the recent health updates I felt a need to. I have cancerous tumors on my stomach and GI tract that were found within the last month or so. She said cervical cancer but she was in the correct region of my body. Thinking about it send chills down my spine. I will be having surgery to remove the three tumors next month and the doctors are sure everything will be ok. The surgery is with a scope that is placed down my throat and depending on if the tumors are attached to the 4th layer to my stomach and GI tract another surgery will have to be performed. I’m claiming that I will not need the additional surgery and that is it.
This is what I have decided to tell all of my friends that want to come see me. I can’t remain in a bubble and not allow myself the pleasure of socializing. I’m tired of hiding behind fear. I told myself that 2016 was going to,be different and so far I haven’t changed from 2015. I’m letting fear run my life and hiding behind lupus. I’ve started a FB page dedicated to my lupus journey and giving updates as they occur as well as daily activities in my life. I truly doubt anyone is interested but I’ve had close to 30 of my friends join and like the page so we will see. My sissy told me I need to make my posts shorter and not articles so I will work on that. My first visitor is my bff from junior and HS and I can’t wait to see her. Love.
Sometimes I ask myself, why me? Then I think is that selfish of me to ask that question? I think it’s only human and God understands. I’ve been in the hospital a lot lately and after not having been in there but once a year or so lately, it’s a reminder of just how sick lupus can make me. My appearance has changed, I’ve gained weight, and my mood and personality is altered as well. I find myself snapping at my mom all of the time and she is the one that takes care of me. She prepares my meals and makes sure I’m following my renal diet, low carb diet, and low fat diet. I’m preparing my body for when I may need a kidney transplant because being overweight is an issue that will put you lower on the list to receive one.its frustrating because I’ve been on this diet for about 2 months and I haven’t lost a pound. I have a lot of bloating and swelling in my feet so that keeps me “heavy” in a sense. I’m not even cheating…lol. I just expect to see results on the scale. My BP is great and my blood sugar is stable, it’s still high but, not as high as it had been. All of this is due to my eating habits. It has been hard to kick my candy habit. I do chew a piece of bubble gum at night while my mom sleeps, we sleep together. I had to kick my dad out and I don’t want to be in my old bedroom because I’m so unsteady on my feet I need to in here with her. Also, since I fainted she really wants to be with me. I’m getting better day by day and I’m hoping to be back home next week, thank you Jesus!!!!! I want to be home in my bed with my things, my kitchen, my couch and just my life. It’s difficult because even though my sister is there she is on her side of the house and we rarely see each other except in the kitchen most times. She says she will help me so it should work out. I’m just terrified of fainting again. I also want to be back to myself when I return home and I know I won’t be and my parents will be over everyday checking on me. I’m such a baby because if they don’t think I’m ready I will probably stay a little longer. But, my home has no stairs so I’ll be able to get around easily as long as I take my time. Moving to another subject, I have an appointment with my kidney doc Wednesday and I’m curious as to what our next steps are and what my most recent labs showed. I’m praying my creatinine is still lowering and my function is increasing. In most cases it’s a waiting game for results and it drives me crazy, waiting by the phone to ring with good or bad news. Lately it’s been more bad than good. I had a ERD I think that is what it’s called. A long tube with a camera goes down my throat and it views my pancreas but while down there I had lesions on my stomach so biopsies were taken of them so I’m anxiously awaiting those results. I got a call today on my voicemail from a doc office I’m not familiar with stating I’ll need to schedule a EUS or EUD to go back down my throat, no one mentioned this to me in the hospital and the docs name wasn’t someone I knew, I’ll call tomorrow to get clarification. It is 3:33am and this is the second night of no sleep for me. My mom says just close your eyes and fall asleep, if only it were that simple. I still don’t think she fully understands insomnia. If you can sleep during the day why can’t you sleep at night, is what she says. I really don’t get it myself but, it’s real and I’ve read definitions online but, her questions throw me off and I have no answers. She’s laying beside me silently sleeping and I am so happy I still have her here to love on me and I know the time will come when our roles change in each other’s lives. Yes, I will find my energy and do whatever needs to be done along with my sister to make sure she and my dad have every single thing they need well into their 100’s, yes I’m claiming it, that I will have them both that long. I’m just cherishing the time I have now. I stare at both of them a lot as if I don’t want to forget what they look like…lol. Hart to Hart is on tv right now, I love it, along with Matlock and Columbo, that was random. Well that is all for now, I will post again when I get results or get proper clarification of the new procedure, or just want to type. Take care all of my followers and thank you so much for simply being interested in my life. Love.
Recently I’ve had two childhood friends want to visit me. One that lives out of town and the other is local. I am hesitant because I feel as though I have nothing to contribute as far as conversation except my failing medical condition and that is highly boring. My mom is telling me that I should see them and just talk and catch up and if nothing else listen to them talk about their life and how it is. This would be great if I were close to having what I thought I would have at this time in my life and I do not. My life is depressing and sad and to hear someone talk about what I thought I would have at 42 is further depressing. I am happy for my friends having spouses and children but, I do not and I won’t because of this disease that has robbed me of everything. I know it could be much worse but what it is is pretty bad to say the least. I feel like I don’t want to be seen by anyone with the exception of family and my sister friend, whom I will see next weekend and I am so so so excited. The plan is for her to come up from or over from Indy and Saturday we will get together early go to lunch and just spend the day together talking, me venting to her and just having a come to Jesus session Which I really need right now, I wish my sis could be there but she’s going to a wedding of a coworker. I’m not sure if we will chill at my moms house because that is where I’m staying right now or my house. I think my house would be better. I will also have to convince her to talk a selfie and ,et me post it on FB, for some reason it makes me feel human and that I’m doing something besides sitting in the house but, I will respect her wishes if she says no and simply have her take my pic saying I’m out with my sister friend…lol!! I told my sis about the outing and her response through text seemed a bit different. I skied her if she felt left out and she said no but I sensed something different. She has been looking forward to this wedding for awhile and I had forgotten and I asked her if she wanted me to go with her but, her hubby is going. It’s hard to read my sis and then trying though text is damn near impossible. At this point I can only go by what she has typed me. So now an update on my health. It’s not great. My kidney biosy went ok but while they were in there they injured my kidney causing a tiny bleed. I then had very bad back pain afterwards and was told it was because of laying flat for 24 hours after the procedure. I’ve since been hospitalized for it and after X-rays was to,d it was probably muscle or skeletol issues not the bleed from the injury. I also had other issues as far as my creatinine being high and my BUN which deals with the kidneys being very high and my iron being extremely low. I was watched for a few days and then let go. It looks like I will be starting dialysis a lot sooner than we had initially anticipated, which is totally scary on a whole other level. I was told that I would be placed at the top of the list but, would be told I need to lose weight to put me even higher on the list. I am hoping my sister is a match for me but, you never know. Ice also had several of my high s hold friends offer to be donors if they match, which blew my mind. I to,d them as we get closer to that I would keep them informed on what they would need to do. I see the love that others have for me and it’s truly overwhelming. They are telling me that they want to see me or simply come over and sit with me to talk to cry or whatever, it’s just so nice of them. I don’t ask for help ever and they are waiting for me to. I have everything I need from my parents and I’m well taken of. I tell them that but, I guess companionship from friends is what I do need because it is missing in my life. Back to health, to get my weight down I may have to have the sleeve operation and after losing weight from that my doc doesn’t think it will be long before I am matched because I will go even further up on the list. It’s all very scary and at the same time I hope it works in my favor. It’s 5:10 am and I haven’t been to sleep yet. It happens this way sometimes, despite taking my sleep aid and pain meds I’m up all night because of my insomnia. I am thinking my friend from ,out of town I will visit with but, the local friend I may ponder that a bit and the reason is the relationships were completely different. Any advice is welcome. A bit more info is that the out of town friend is a female that I’ve know since I was about 7 or 8 years old the other I met as a teen and he is a male who I got very close to for years after. That is all I will say so figure it out..lol. It would be a very innocent meeting between us since he’s married now but he has a very big heart when it comes to those he cares about. I will keep,you updated.
I am drawing a blank and that is pretty sad as an American. My dad is a veteran but, I thought memorial meant to memorialize and my dad is alive and well ( knocking on wood). My grandfather served and he’s passed away so I celebrate him today along with my Uncle Snap and Uncle LC.