Ashley Updates

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  • Update 4/21

    Praise be to Jesus Christ.

    Sorry for delay in update. Hope this makes sense and I am not being a complainer.

    These couple weeks have been difficult. Sometimes I didnt know what was real. A wise friend encouraged me to write down what I know to be real.

    What is real:

    God is real.

    He loves me and died for me. His love and mercy is poured out for all sinners.

    Mother Mary has me wrapped in her mantle and brings me closer to my Lord.

    My husband loves me, is always by my side through everything. He cares for me and loves me even when I can’t do the same.

    My children love me and I love them just in a different way right now. I pray for them and try to cuddle when I can.

    I am never alone.

    My parents, family and friends are always with me and love me, my husband and children.

    Our community is amazing and your support is beyond all imagination.

    God only gives thoughts of peace and love.

    Many more

    **LIES I get trapped in: There are many.

    I am not a wife.

    I am not a mother.

    I am just being dramatic.

    I am faking it.

    I am unlovable.

    Should be alone and dont deserve people to care or love me.

    I despair and cry out to God.

    I think everyone would be better without me.

    I am a burden.

    Many more.

    A couple weeks ago Damien took me to er because I was having seizures every 3 min. And not aware of them. I didnt know what was happening or what was real. I couldn’t figure out time or reality. The seizures slowly got better over the past couple weeks with more meds. I only have a few a day, they are shorter and am usually aware at least for some of it. Sometimes still hard to know how much time passed or what is real. My friend said to hold a crucifix if I cant figure out what is real. Damien will put it in my hand if I can not. I feel I am beginning to come out of a deep thick fog. (Like in the Tangled movie song) *Its like the fog has lifted * Sometimes it comes back but it is much better and I just remind myself what is real.

    Radiation is harder than I thought and I look forward to the weekends, especially Sunday when I get to go to mass. I love mass. I am half way done. I speak slower and slurred sometimes because of the radiation on my motor areas. It makes my lips and tongue go numb. A lot of my hair is falling out. Damien calls it my monk tonsure. Lol.

    Damien and I just had our 12 year anniversary of entering the Catholic Church. We are so blessed. It has been amazing. Thank you to Lisa and John Neilsen for sponsoring us and sacrificing so much to help us through the process and are still there for us now.

    Lord, it is hard but I offer myself as a living sacrifice. I give you all of my joys and sufferings. I surrender myself to you and will trust in You. Forgive me for my weakness and be my strength and refuge.

    I wish I could write a nice thank you letter to every single one of you. You are all so generous, so kind, and showing us God’s love. We love you all.

    God is so good to us.

  • Update 4/6

    Dear Friends,

    He is Risen!! All Praise and Glory to God!!

    Sorry for long delay between posts. Been a roller coaster.

    We have a team of help, prayers and support that have rallied around us. My dear friend Heather came out for a week. Her and her family sacrificed so much for her to be with me and my family. Im very thankful to her, her family and all the sacrifices of all the people that have helped on daily and weekly basis in our home. We would not make it without you. Im thankful to all the people that offered prayers, donations, cleaning, helping with children, texts, calls and visits.

    I started radiation on 3/26 M-F. Radiation is quick. I ran out of seizure meds and didn’t realize how much they helped until I ran out. Damien was amazing and managed to get me more at midnight after missing 3 doses. I felt better after that.

    Easter was a blessing. I made it through mass, Praise God!

    Our community is amazing! Did I tell you that!? They put together Easter baskets for all the kids!! They are better baskets than I was ever able to do for them. Gods love and mercy is being poured upon us. Thank you to whoever put these together. It was a huge blessing. The kids were so excited to open them.

    Father Anselm came over for a short visit with us. Which is always a blessing, but i felt bad as we didn’t have much to offer him.

    The whole family went to my Aunts house. I made it through appetizers and egg hunts. I laid down after that and kids spent time with family. We left later and saw a gorgeous Sunset!

    Today has been hard. I feel more tired and more difficulty thinking. I’m also struggling with thoughts and working them. I praise God for all the blessings and all the difficulties.

    Fr. Ripperger in a podcast compared this life to lent and heaven to Easter. Im trying so hard to keep this in the front of my mind. What does suffering matter if the reward is heaven for all eternity. Of course this is much easier said than done. My sin is great, because lent is hard and feels like a huge mountain you can’t climb.

    I know i have been given more support than I deserve and this is what makes me so weak. Even with all the support, I still feel like i am drowning. Please don’t ever assume I have it all together. I do not. One step in my house and you will see that. Im struggling like everyone else. We are all given heavy crosses to bear. I am blessed with support i don’t deserve and feel others dont have the support they do deserve. I love you all and am grateful to everyone.

    God bless you all,

    Ashley

  • 3/24 Update

    Dear friends,

    Praise to you Lord, Jesus Christ. My Lord and my God has greatly blessed me. Thank you all for the outpouring of love, generosity, and support. It is supernatural.

    I have decided against posting my reflections post at this time. My emotional state is in a bit of turmoil and my perspectives may be skewed and taking away from the glory of God. Once I can parse through and navigate them better, I may try again.

    Friday 3/20 I had 2 long appointments for radiation prep. I thought the first CT scan, simulation and making of mask would be the harder appointment, but it wasn’t. Everything was fairly smooth and quick. The making of the mask was a bit painful when they molded it around sensitive areas. Other than that it was fine.

    My 2nd appointment was the brain mri. This ended up being the longest and most difficult mri I have had so far on this journey. It was over an hour of loud noises, laying flat, and not feeling well. The radiation tech was very kind. Her name is Wendy. She had to pull me out a few times for contrast and to stick a sticker on my right forehead and temple area. Im not sure why but this caused the scan to take about 20 min. Longer than expected. Wendy made sure I was OK and talked to me through everything. Im very grateful for her.

    I came home Saturday evening! It has been difficult but good. The kids are doing better having Damien and I home. It can be overwhelming and over stimulating, but I know it is best. It is easier for Damien to be with me and kids. He is not torn in so many directions.

    Yesterday 3/23, I had an appointment in City of Hope Duarte with a neuro oncologist. I really liked him. He was thorough, tried to get to know us a little. Made sure all our questions were answered. He discussed the focal seizures and his concerns about them increasing during radiation. Damien and I feel he is the best choice for me. He did say no to the cruise we had planned in May. We are in process of seeing if we can postpone to the fall.

    Radiation is officially starting March 26th for 6.5 weeks, Monday through Friday in Orange. Please pray this goes well, with least amount of side effects. Praying this works and cancer does not return, if this is God’s Will. All Glory and Honor to God.

    God bless you all,

    Ashley Dennis

  • Prayer Requests

    Dear Friends,

    Our family has received an incredible amount of love, generosity, prayers and help from so many people in our community and strangers. We are in awe of it all. I was trying to figure out a way I could even begin to help you all. Everyone is going through their own struggles and is carrying their own heavy crosses. A very small and meager way I can give back to all of you is to pray and offer up everything for you all.

    Will you please text,email, or comment here your prayer requests and I will daily keep you all in my prayers and offerings? You can be as specific or vague as you want, but please allow me the privilege of serving you in this very tiny way.

    I will post another update at the end of the week with pictures but for now this is all Im going to say. Love you all and May God bless and reward you all for your love and generosity to us.

    God Bless,

    Ashley

  • Update from Parents house

    Dear Friends,

    im sorry for time between updates. I haven’t been feeling well and its been difficult to find energy to update.

    God continues to take care of everything so perfectly. Maybe I can explain in more detail later but for now it will be brief.

    Focal seizures get worse at times and have spread to both sides of my body. I have more up and down days compared to last surgery. Not steady improvement. Kids are happy to be able to see me and cuddle but I can only handle very short visits which is difficult for everyone. I want to be with them all day but im unable to do it. Makes my heart ache and makes them cry. Trying to navigate it all so they dont think im pushing them away but trying not to exhaust myself. Please pray for my children. It is very difficult on them.

    I spoke with UCI radiologist and liked him very much. He was patient with all my questions, considered them and thoroughly answered and explained everything. He made a plan and made sure I understood what was going to happen and all side effects even rare ones since those seem to like me.

    The plan:

    6.5 weeks of radiation with sessions every weekday trying around same time. More aggressive with dose and area. Goal is to start ASAP, March 26th or sooner. I will be going to Orange, Ca for treatment! Praise God for His provision. The best treatment for me is so close and will relieve a lot of stress on everyone because it is so close.

    I get my stitches removed in Duarte on Wednesday. Once cleared from neurosurgeon can start process for radiation.

    I was hoping to go home tomorrow but I am not able to do that. I will be at my parents until at least Thursday or Friday and very likely into next week. My parents are amazing and I am comfortable here. Kids are able to easily come over and they stay downstairs and come upstairs for short visits.

    God is good to me. I am having a more difficult recovery but I will join my suffering with His, offer up everything and I am praying for all of you. Please text me specific intentions and I would love to pray and offer up everything for them.

    I was able to walk down the hallway with my (AFO),ankle, foot orthopedic. I can bend my knee and move my toes a little more. Physical therapy will come on Tuesday and Thursdays.

    I will try to update again soon.

    God bless you all.

    Ashley

  • 1 week post surgery update

    My dear friends,

    Thank you for the overwhelming love, generosity, and support we have been so unworthily receiving. God is pouring His love and mercy over us all. It brings me to tears to witness and I will never be able to thank you all enough or express my gratitude for it all. Praise God for all His blessings and endless mercy.

    God has truly laid everything in my lap this week, telling me to surrender, trust and He will take care of it all. He has truly taken care of everything and more. I love you my Lord and my Savior. Help me love you more.

    Father Anselm was able to get us in touch with a priest who came Sunday and we received Our Lord. What a blessing!

    A Huge Update:

    I had a telehealth appt with a radiologist from UCSD to discuss receiving 6 weeks of Proton radiation there. This was recommended by MD Anderson. The doctor came in the call and confidently told us that Proton radiation is not the right way to go. She agreed with my neurosurgeon and said it is still too targeted and my cancer is too aggressive to use it. She said I need someone that specializes in CNS brain tumors and has experience with ependymoma. She was confident that this is indeed supratentorial ependymoma with zfta-fusion positive. She recommended a doctor at UCI and said he would be perfect and I can receive my 6 weeks in Irvine, ca!!! Praise and Glory to God! I don’t need to go to San Diego every day for 6 weeks. This will be an incredible blessing and so much better for the children and our family.

    She did emphasize several times that I can’t wait and need to start as soon as possible because it grew back in 3 weeks last time and is very aggressive.

    Another miracle by my Savior is that besides already being a patient at UCI, I have a friend who is a nurse there. My friend had already gotten me in touch with the doctor she works for before my surgery. I was able to talk with her and ask if she knew the recommended doctor. She does know him and was able to expedite me getting in for an appointment. I have a telehealth appointment with him TODAY!! How incredible is God. Why am I so blessed that He is laying everything in my lap so perfectly? Im overwhelmed by it all. I will post another update about this after the appointment.

    A few updates:

    Damien bought a standing walker and the walker that was suppose to be here Friday was delivered Tues. Afternoon. Praise God!

    I received my custom ankle, foot, orthopedic brace on Monday as promised. It is honestly a game changer. It helps my stability so much and will help me be more independent quicker.

    I started physical therapy Saturday and then had it again Wednesday. I love the approach of this company. They are not interested in checking boxes. He explained to me that my problem is not strength or ability, it is having my brain create new signal pathways in sensory and motor areas. He explained how I should try not to compensate because then I will be training my brain incorrectly. I might not get back full functioning. He told us that it is about correct repetition (1000s of times) doing the correct motions and it doesn’t need to be me physically walking so many feet, it is me in bed doing repetitive correct leg and foot movements. He told me to be patient because I may not see progress for a long time until my brain creates the new pathways and then it might be sudden and great improvement. I have seen improvement this week which is great but he wanted me to know that if I stall not to give up or think it isn’t working which I really appreciated. This company doesn’t usually get to follow patients home but in God’s great love and blessings they were approved by insurance to follow me home. (After last surgery I never fully regained use of my left leg, physical therapy did teach me to compensate so Im hopeful this time that I will gain full functioning back.

    This week here has been the perfect recovery place. It has definitely made up for the difficult hospital stay.

    I have had more and different symptoms and struggles this time around.

    Im still light and sound sensitive and too much stimulation is overwhelming and hurts. My left leg is weak, less sensation. My left arm is weaker but still functioning. The difference this time is he did surgery in a new area thats a motor pathway so even though I have less sensation in my leg i have a lot of muscle pain, stiffness and cramping in my whole leg and foot. I am unable to move my leg to relieve any of the pain or cramping. We realized I was getting focal seizures in my face, neck, arm,stomach and leg on left side. The doctor doubled my anti-seizure meds. Im still getting them but they have greatly improved. I have had more up and down days than I think I had last time which is fine, its just different. My headaches are more manageable which is a huge blessing.

    We have such an amazing faithful community that provided us today another huge blessing. I had 2 friends drive an hour or more each way and take turns staying with me so Damien could go home for over 5 hours to spend time with the kids. He said it was incredible. The kids were all over him and they needed it so badly. He cuddled them, took them to the beach, talked with them. It was so healing for all of them. Im so incredibly thankful. God has given us friends who know no bounds to love, generosity and sacrifice. Im so undeserving. I miss my kids so much and cry for them. I can’t wait to see them, hold them, and be with them.

    We will check out from here Friday and I will stay the weekend at my parents house. On Friday the kids will come over to parents house and come to the room 1 at a time to cuddle and talk to me. Im looking forward to this immensely. This way they will each get time and it won’t be overwhelming for me. It will also give them an idea of how I am so they know what to expect and how to behave around me when I get home. I will see how Im doing by Monday and go home if I think I can handle that.

    Thank you for bearing with these long updates. Thank you for your prayers, texts, calls, visits, generosity, meals, support, encouragement and friendship. God is pouring blessings and consolation over our family. Praise and Glory to Him now and forever.

    I want to post a reflection and random thoughts post before I go home if anyone is interested.

    God bless,

    Ashley

  • City of Hope Post surgery update/City of Hope Hotel

    My dear friends,

    I apologize for the delayed update, it was a mixture of many factors. Sorry for the very long update, please bear with all the mistakes and I hope it is clear enough.

    Praise and glory to God for a successful surgery and for His love and mercy He has been pouring out over me and my family. I love you Lord.

    When surgery was over, Damien was not with me. I asked and begged for him many times. I was told he would be called and come. We figured out that they didn’t call him for an hour or more. I was on verge of tears begging for him and was very relieved when he got there. My first 36 hours were difficult. Damien said the first nurse was very impatient, inattentive and rude to me. I don’t really remember much of that. Sometime in the evening I asked to eat. The night nurse told us their protocol is to have the speech therapist sign off on the patients ability to eat and diet. She told me I had to wait because the speech therapist had gone home and couldn’t tell us exactly when she would be back. I waited longer and asked if there was anything I could have, I was so hungry. Eventually they allowed me to sip chicken broth and apple juice during the night. On Wednesday the morning, they could still not tell me what time the speech therapist would be in to sign me off to eat. I could clearly talk and swallow but the one lady I needed to sign off was not there. Sometime after 8am on Wednesday, I stopped eating at 8:30pm Monday night (36 hours), we asked again, the nurse still did not know when the speech therapist would be by. Damien got upset and told the nurse he was going to get me food and be responsible for it, but I needed to eat. I know it was difficult for the nurse because she needs to follow “protocol “. It seems they need someone else to be able to sign off when speech therapist is not available. The nurse was very kind and eventually allowed me to eat soft foods. I ate around 10am, over 36 hours later. The speech therapist ended up coming in a little after 11am and signed me off for regular diet. I was happy to be able to eat. I had a couple great nurses in the icu (Darla and a night nurse who we unfortunately can’t remember her name)and things were better. Wed. Night they told me I was going to bed transfered out of icu. I was experiencing right side weakness and a ton of pressure behind my eyes and front of head while still in icu. They took me in for a ct scan and it showed Pneumocephalus, which is a collection of air or gas in the brain from surgery. They put me on oxygen to help get it out. It did help a lot.

    At midnight I was transferred to the general surgery floor, they had warned me that I may need to share a room. I was very nervous about this because I am very light, sound and stimulation sensitive after surgery. Praise God I was able to get a private room. When I arrived I there were 2 nurses that greeted me. One was training the other. The nurse being trained had seen in my chart that I had 8 children. She was very loud and was talking to me about kids at midnight. I didn’t want to be rude and tried my best to engage. She then began to loudly tell me stories of her son and was literally jumping in my room to show how her son likes to try and touch the ceiling. This was very challenging. The other nurse helped me and told her she needed to be quiet and calm down. Keisha was an amazing nurse. The rest of her shift she made sure everyone who entered was quiet, calm and to keep the lights low or off. I heard her tell another loud nurse to be quiet and the other nurse said she was about to leave. Keisha said OK. She was advocating for me, very attentive, made sure I was comfortable and that my oxygen stayed on. The pressure was much better by Thursday and they did an mri said it got much and it didn’t need the oxygen anymore. They did see a sinus infection above my right eye and put me on antibiotics. Thursday was another difficult day. At shift change it was so loud, there was literally nurses hooping and hollering. I learned later they were celebrating a nurse receiving an award. I dont know if it is the building or nurses or what but that floor was constantly so loud. I could hear all conversations, machines going up and down the hallway, trash cans slamming, things being hit against walls. It was awful. Thursday I had physical therapy come and a lot of people constantly coming in. I only got to take a 30 min nap the whole day. I was exhausted and the noise and lights were bothering me tremendously.

    Damien and I were doubting our choice to come here because our after surgery experience at hoag was drastically different. Also on Thursday, with all the people coming in I hadn’t seen my nurse in 4 hours. My head was hurting badly and it was time I could take pain meds. I pushed the nurse button and they told me she would come. 30 min went by and she hadn’t come, so I pushed the button again and told them she never came. She was surprised and I could hear her tell my nurse to come to my room. She finally came and gave me the pain meds.

    All Thursday was loud and busy but a lot got in order and they told me I can be released Friday. Thursday night was another difficult night with loud noises and lights, I was exhausted and it was difficult to sleep. Friday morning, I was talking to the nurse about the noise level and she was surprised when I told her I heard many things from her morning meeting at shift change. I told her some things I heard, and she was surprised I could hear that. You can hear everything! She did say that their floor is notorious for being loud and they got 3 grievances last week because of the noise. Maybe I has to do with how the building is constructed, I dont know but they need to find a solution. I also think that if they do not have a separate floor for neurosurgery, the nurses need to be trained better in the side effects that a neurosurgery patient has verses someone who had surgery on their abdomen or other body part. They need to be aware of light, sound and stimulation sensitive patients. They think they are being kind and caring when they come in, turn on the lights, greet you with energy and talk with you. I don’t blame them, they just were not aware.

    I was complaining to friends and my parents. I needed to complain less, suffer better and offer it up.

    On Friday morning, Dr. Badie came in and explained more of the surgery and what he found and took out. There were 3 sections. 2 in front were connected. The front he said was all scar tissue that he removed. The second section was scar tissue and tumor mixed. The last section which was separated was all a new tumor. He did not need to cut anymore skull which was wonderful and I feel less sensitive than i did after first surgery and the pain has been much more manageable this time as well. The incision is also shorter than the first time. He talked about radiation and explained that he thinks the Proton radiation might not be the best option after all because it may be too targeted as well. He suggested getting radiation with a larger margin to ensure they kill everything around it that might be microscopic now might be better to prevent regrowth again. Dr. Badie talked to Dr. Schwer from City of Hope in Irvine. She did the Cyberknife radiation on me and is an amazing woman. I trust her and like her very much. I will make an appointment when we get home to discuss all this.

    I was approved to stay in the city of hope hotel for a week. 4 nights being covered by insurance and having pt come to me there.

    At discharge, they told me a walker and bedside commode that I can also use as a shower chair would be delivered to my room that day. I was released!!

    A wonderful man named Tom wheeled me out and brought us to a shuttle that took us to the hotel.

    This hotel is amazing. We have a studio with full kitchen, living area with couch, and bed. It is quiet, calm, peaceful and very comfortable. I immediately felt so much better being here. We will stay here until Friday. The only bummer was that my walker and bedside commode were never delivered. We spent over an hour on hold with the company and no one ever answered. They hospital didn’t know why it wasn’t there, the hotel didnt receive any notes on it. The physical therapist came by and said he got an email saying it was delivered to my house. I had the older girls check and nothing was delivered.

    Yesterday, 2 of my friends brought Leah and Eden to visit me at the hotel. It was wonderful to see friends and the older girls. I have such amazing friends and family. God is so good to me. My parents ended up being able to come visit at dinner time and they brought me a friends shower chair so I can shower today. It was encouraging and uplifting to see them. I was able to sit on the couch and visit with everyone.

    I still don’t have a walker but Damien has been looking online to buy one. Damien is incredible as always, helping me and caring for me the whole time. He did find a wheelchair nearby and bought that.

    The whole time my incredible family and friends have cared so beautifully for all the kids. I didnt have to worry about them. I miss and love them so much but im at peace knowing they are so well cared for.

    im doing well now and praying for all of you and trying to offer up everything and suffer better. God is good to me. God bless you all and thank you for everything. Im sorry if this post is all over and I hope it makes sense and is not too much complaining. Im surrender to Our Lord and need to trust in Him.

    God bless,

    Ashley

  • 3rd Operating Room Update

    The surgery went well and Ashley is being prepared to leave the O.R. Dr. Badie said that some of the tissue that was suspected to be re-growth based on the imaging turned out to be scar tissue. He was able to remove the tumor regrowth as well as scarring. He said he expects Ashley’s left leg will be weaker before it gets stronger again.

    Lord, thank you for your providence and the skill of the doctors working on Ashley. Thank all of your for your continued prayers!

  • 2nd Update from the Operating Room

    Ashley is still doing well, everything is going to plan though the surgery seems to be lasting longer than anticipated. I will update again once I hear anything more.

  • 1st update from the Operating Room

    The procedure has started and Ashley is doing well.