Sorry I haven't written in a while, I have just been tired and busy with appointments, treatments, and seeing friends. Anyway, a lot has happened since I last posted, both good and bad. But I'll start with the good. About three Saturday's ago I got to go to my dear friend Caitlyn's Senior Prom with her, and we had a blast. I met Caitlyn a few years ago at y support group for kid's with chronic illnesses, and we immediately hit it off. Not only do we both understand what its like because of our illnesses, but we have a lot in common besides that. She is a year younger than me but we don't care, and because she also is an only child we view each other as pretty much like sisters. Its also nice because our mom's our good friends and they can have someone that understands what its like to take care of a chronically ill child. Lets get back to the prom. So Caitlyn invited me to go with her because since I wasn't able to go my senior prom since I couldn't go to school she thought it would be fun to go with her. We were each others "dates." She goes to a private Christian school and there are only about 14 kids in the senior class so the prom is for all the high school students. All 4 high school grades make up the size of 1 senior class they may even have fewer kids. Before the prom me, Caitlyn, her mom and my mom went out to dinner at an italian restaurant and then headed to the prom at the Marriott in Horseshoe Bay. While we were at the prom our moms went out for a margarita and coffee. The prom was fabulous I knew a few of Caitlyn's friends and I met many more. Everyone was such open arms, they told me that Caitlyn told them all about me and how she admires me, it was so sweet, it just reaffirmed want a true friend Caitlyn is. After the prom we went back to Caitlyn's house watched TV for a bit and then went to sleep. The next morning we went to breakfast and just had girl talk (mom's included). The weekend was a blast and it was such a fun memory, and now I can say I got to go to the prom.
Now for the bad. The Tuesday after the prom I ended up in the ER. What happened was, I had gotten up to go get my GED workbook, and my foot had fallen asleep from being swollen. I had gotten up to try to walk on it with my walker to wake it up the first step I took, my foot rolled, and I could hear and feel it pop. I screamed from the pain and my grandmother came rushing in. Now I have broken about 7 or 8 bones so I know the difference between a sprain or something fractured/broken. My foot immediately swelled to twice its size and my grandfather came home and took us to the ER. The doctor who first came to see me was just about to leave because his shift ended but he wanted to examine me before he left. He said that because of the way it rolled that it most likely was broken and he had seen the similar cases before. They did an X-ray and a new doctor came in and said it wasn't broken so we were relieved. However a day later it started to bruise and swell more and was getting worse and my home health nurse decided to take a look at it and said I needed to go get it checked by an orthopedist because there probably was a hairline fracture. So on Good Friday I went to see the orthopedist who has treated both my mother and grandfather. He took a look at the X-rays and my foot and thought it was a bad sprain, he then said it could be a hairline fracture and if it is it is so small its hard to see on the X-ray. He ended up putting me in a walking boot cast and said come back in three weeks and they'll do more X-rays. On top of that same week I came down with a bad cold and had to be put on antibiotics but luckily I was well enough to goto church on Easter. Then last Monday I had chemo and have been feeling miserable from it. My oncologist here in Austin is concerned because my muscles and joints are getting worse and she is concerned and almost didn't give me my chemo, she said i didn't look good. I got to San Antonio to meet with Dr. Patel on the 26th to discuss possibly a new treatment plan. They don't know what to do because the chemo has helped the lesions on my SI joints from the AS but it hasn't helped my RA or myositis. I am nervous about what's going to happen, but I know that it is all in God's hands and I need to have faith in him. I'll keep you all posted and try to blog more frequently.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
My name is Alexandra Acosta, I am 24 years old and am living with Muscular Dystrophy (MD), a progressive genetic muscle disorder with no cure and no treatment. This blog is to chronicle my journey about living with MD and all the ups and downs that it entails. I hope that this blog inspires people and helps them to know that living with MD is the craziest ride of a lifetime.
Monday, April 16, 2012
Sunday, March 18, 2012
Leading A "Normal" Life
For the past couple of weeks I have been working with an OT who comes to my home. He has been teaching me exercises that help to keep me from losing muscle strength, and to slowly help me increase my strength. We also work on things such as ho to conserve energy and to learn how to use adaptive tools to help me live a normal life. One of the things that we were talking about is how my grandfather wants me to live a normal life and be like any other 19 year old. I want that as well but my OT says that my normal will be different then his idea of normal. For people who live with a chronic illness or a disability our version of a normal life is different from that of a person who isn't in that situation. We learn to adapt to the world us, how to cook and make our own food, how to get around buildings so we can work, go to school, or go out, and how to take care of personal hygiene. Sometimes it can be more difficult than it would be for a healthy person, and sometimes we have to use tools or devices just to get through a day. But, just because we do things a little differently doesn't mean we are not leading normal, happy lives.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Sunday, March 4, 2012
Infertility and Chemo
Being on chemo has many risks, one of those risks is infertility. different chemo drugs have a different risks of making someone infertile. The particular drug that I am on has a high risk of making me infertile. When I started my treatment I new that their was a chance of infertility but I didn't know how much of one. I recently saw a fertility doctor to see about what I could do to preserve my fertility. Due to the fact that I have already had 6 treatments my ovaries have already taken a hit. A woman of my age usually has between 10 and 20 follicles I only have about 5 or 6. The doctor than developed a protocol where today, I will begin to take hormone injections, as well as the oral medication I started on Friday to stimulate my ovaries so that I can have my eggs retrieved and then frozen. I will need to be on this medication for up to 14 days. There is a chance since my ovaries have taken a hit from the chemo that the stimulation medicine wont work and they cant retrieve any eggs. But we are hoping that is not the case. Please keep us in your prayers, and that I am able to save and preserve my fertility.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Friday, February 24, 2012
Losing A Friend
Last Saturday I received some very sad news that a dear friend of mine passed away from a lifelong battle with Cystic Fibrosis, he was only 21 years old. He had a lung transplant earlier last year and had been doing well and then started going into rejection but was stable, then in December before Christmas he ended up on a venelator in the ICU, doctors said his only hope would be another lung transplant, but he wasn't strong enough. His mother had to make the decision of turning off the machines. However, he woke up and said he wanted to fight, the doctor said that it was a miracle that he woke up and he had not seen anything like it in all his years. Still on the venelator he was number 1 on the transplant list. Sadly he eventually said he no longer wanted to fight because he felt that the chances of recovering were very slim, and he wanted somebody else who really needed a pair of lungs to get them. He bravely chose to die peacefully with his mother and brother by his side.
Finding out that he passed was very sad, but I was happy that he was no longer in pain and he was now home with God. My friend had always been an inspiration and a beam of hope and courage and he will be greatly missed. I sometimes ask myself why good people like him have to die, but that maybe something we can't explain. We must accept that God wants us all to eventually come home, whether we as individuals or our families our ready. Everything happens for a reason.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Tuesday, February 7, 2012
Going Past The 3 Month Mark
When I started this 18 month long treatment, the doctor said that at about 3 month mark they would have to evaluate my progress to whether or not to continue with the treatment or go on to something else. Well I am pleased to say that I made it past the 3 months and this month will be my 6 month of treatment (give or take). According to my test results my SI joints look really good, which means the chemo is working. I still am having challenges with pain, swelling, and stiffness in my joints and still have difficulty walking. I am working and fighting very hard each day to get better and get back to having a normal life. I still have about a year left of treatment, and I am planning to get through it will all the strength I possibly have. I know that I could not have gotten this far without the support of God, my family, friends, and my medical team. I know that each day is a new day and I am thankful that God has allowed me to be able to continue to live each day to the fullest.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Saturday, February 4, 2012
Sitcoms For The Sick
Being home quite often, and having days where I just can't do anything because I feel so miserable, I try to find different things that will cheer me up. One of those things happens to be watching sitcoms. Some of my favorites are a bit older such as the Golden Girls or the Nanny, but i also like watching the more recent ones such as Still Standing, Reba, Will & Grace, and The New Adventures of Old Christine. Watching these shows provides me with a sense of common relief and often perks me up. My grandmother always tells me to watch something funny so that I don't have depressing and negative thoughts, and watching sitcoms is a way for me to do that. It doesn't even matter what the subject of the episode is, as long as I can get a good laugh out of it. So if you ever find yourself in sad or depressing mood, sick or not, turn on a sitcom. You may think the episode is completely pointless, but I can guarantee you that something in the episode will give you a good hard laugh and perk you up.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
Wednesday, January 4, 2012
New Years In The Hospital
Sorry I haven't posted in a while things have just been a bit crazy. The new year for me did not start out very well. Over the past month my right hip has been bothering me very much and for a while I thought I could just continue taking my breakthrough medication to cope. When I went to visit my pain management doctor last Tuesday he added Percocet as a new breakthrough medication. However it didn't work, and then hospice tried to tweak with my meds. My pain got so bad that they finally told me to go to the ER, and I was admitted early Saturday evening. The doctors and even my rheumatologist who was on call thought it was the AVN that I was told I had in both hips. The MRI was a bit fuzzy so it was hard to read. I was given IV Dilauted, and Roxycodone for the pain, and IV Benadryl, because the Dilauted caused itching. On Monday the orthopedist came buy and said that the AVN that was there in August of 2010 had healed itself, which was a relief, because it meant that I didn't need surgery. He was puzzled by wht could be causing my pain, so he wanted my rheumatologist to take over. Luckily, Dr. C had a pretty good idea what the problem was after learning that the AVN was gone. He suspected that pain from my Sacroiliac (SI) Joints was causing the pain in my hip. Pain in the lower back can radiate into the hip causing the patient and the doctors to believe that the pain is originating in the hip. Dr. C then said he wanted my SI's and hip to be imaged at an imaging center outside of the hospital. He wants someone to come do PT with me at home due to the fact that my immune system is to weak for me to do physical therapy at a therapy gym. After the new MRI's are done we will be able to isolate the problem and make me comfortable. I was released yesterday and am glad to say that I am now home, and doing better, though I am still in some discomfort.
I also went to San Antonio to see my Hem/Onc doctor there. My blood tests show that my white blood cell count is low, which means that my actual bone marrow is suppressed, this means that the chemotherapy is working. There is some improvement in my joints so we will continue with the 18 month treatment plan. My blood clot is also 1/4th the size that it was, so that means that the blood thinners are working. Hopefully, I can get a Port-O-Cath inserted soon, so that I can get the PICC line removed from my arm, but we may have to wait until the clot improves even more. All in all I would say that there have been ups and downs, but my family and I keep chuggin along on this roller coaster of a ride. I hope that this new year will bring good new things both with my health, and life in general.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
I also went to San Antonio to see my Hem/Onc doctor there. My blood tests show that my white blood cell count is low, which means that my actual bone marrow is suppressed, this means that the chemotherapy is working. There is some improvement in my joints so we will continue with the 18 month treatment plan. My blood clot is also 1/4th the size that it was, so that means that the blood thinners are working. Hopefully, I can get a Port-O-Cath inserted soon, so that I can get the PICC line removed from my arm, but we may have to wait until the clot improves even more. All in all I would say that there have been ups and downs, but my family and I keep chuggin along on this roller coaster of a ride. I hope that this new year will bring good new things both with my health, and life in general.
Joyful Love
&
Blessings In The Lord
Alexandra K. Acosta
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