Showing posts with label chronic illness. Show all posts
Showing posts with label chronic illness. Show all posts

Wednesday, December 12, 2012

These are a few of my favorite things...

These are a few of my <least> favorite things...

Sorry to take some time on this forum to gripe, but I feel like those of us struggling with various health conditions are sometimes afraid to mention some of the things we have to deal with. I'm tired of "hiding" and just going by the names of the various diagnoses I've had through the years. All the symptoms are even starting to run together at this point to where I don't know what issue is causing what symptom anymore.



Nonetheless, I'm tired of:
  • having to spit out mouthfuls of blood every time I brush my teeth [this pic was after I'd used cold water to try to slow down the bleeding]
  • bruising very easily at times [I never know where the next bruise is going to pop up or how bad it is going to look and how long it will last.]
  • excess layers of skin forming to the point it starts cracking
  • suffering from severe headaches that can often strike with no warning
  • issues that affect my vision - from the headaches to nerve palsies that are triggered to reduced peripheral vision
  • dealing with the pain at the varying degrees, to the point it is now affecting my concentration and memory

Tuesday, October 02, 2012

It's the little things in life...

It's the little things, that I miss the most.

I would like to be able to finish all my sentences (spoken or written) without struggling for words or replacing/substituting words. I am thankful that I have a husband that can truly complete my sentences. I am thankful that my 3-year-old is in sync with me enough that she can tell what I'm referring to when I stub in filler words like this, that, thing, etc. I am thankful for the lighthearted moments I have when she tells me "silly mommy" as she proceeds to correct me; although, these moments still break my heart in some ways...because there is a circumstance in which she has to correct me that I don't really have control over but wish I could control/get rid of.



I would like to be able to wash my hair when I wanted to. I am thankful for a husband that will help me. Currently, he washes my hair for me around once a week. I am afraid this, as well as all the other things that are quickly becoming his responsibility, will put too much of a burden on him. I am thankful he has been sticking around through the hard times thus far. But in a society like we have today, where "..for better or for worse... in sickness and in health..." are merely words stated at a ceremony and not really a vow and lifelong promise, I am scared. I don't want him to feel "stuck"; however, I do want him to tell me if he starts feeling that way so that we can try to figure out what we can do to change things before he feels like leaving is the only solution. I've already been calling around local salons to see how much they would charge for just a shampoo and style. $15 is about the cheapest I've found so far, so now I'm trying to figure out how I might be able to squeeze $60/mo out of our budget so that I can go there...maybe at least a time or two a month...instead of it feeling like all of that is on him.

I would like for my husband to not be "afraid" to touch me. I am thankful that he tries to be understanding. I miss the "tickle fights" we used to have when we were dating and early on in the marriage. That's been traded out for him even asking if he can hug/touch me. He's gotten scared because all too many times he's come up behind me to hug me and I've jumped or pulled away as a reflex because of the pain. A simple touch can send a pain through my body that I would liken to a knife being stabbed in to me. A shower can feel like pins or darts pelting into me. Seams of my clothing can fill like a knife cutting in. This type of pain is definitely not something I "enjoy." I want the aspects of my relationship that I miss back, such as the cutting up, tickle fights, play fights, etc. I also wish that the fear of this pain didn't keep me from playing with my daughter at certain times either. She is definitely a "touch" child, so I feel bad that I can't tickle and play with her at times.

I could go on and on, such as my dread of a simple trip to the grocery store, but I'm going to stop for tonight. I hope I did touch on some of the things I am thankful for in the midst of all of this, especially my husband and daughter! Thank you Lord for blessing me with them!!!


Thursday, September 27, 2012

In all Honesty...

...I hate living in pain every day.

Yes, I am throwing a bit of a pity party today. I know it could always be worse so I don't like talking about the pain and issues I go through very much. However, not talking about it doesn't mean that it's not there. I can't deny it. Maybe talking about it can encourage some others because they will realize they are not the only ones and they are not "crazy" and the pain is not just "in their heads."

It is real; the symptoms that we experience do exist!



I couldn't tell you what the root cause of my problems any more. I do know that at this point I have a running list of diagnoses:
  • Fibromyalgia
  • CREST (limited scleroderma; type of RA)
  • Chronic Sinusitis and Allergies
  • Nerve Palsy
  • Vocal Cord Dysfunction / Paradoxical Vocal Cord Motion
I've also been tested for Myasthenia Gravis by multiple neurologists (on their decision, without my ever stating that I had been tested for it previously, etc). Based on some things I have read, I think this might even explain some issues we had with our daughter after she was born. However, every neurologist has only done the nerve conduction/stimulation test and quit looking into it after those results are not definitive or "negative." Maybe it really is just the nerve palsy that causes the intermittent eye dropping and vision problems. Maybe it is just the PVCM, which I wasn't diagnosed with until this year, that causes the issues with swallowing, etc. Who knows why I feel like I struggle to hold my neck up and feel like I can barely move my arms and legs at times. I'm not the doctor and can't diagnose myself, but this condition keeps coming up during visits with various doctors across the past 10 years...but I can't add it to my list yet.

I used to think I would end up getting the right combination of doctors and medication and all my problems would be solved. Now, I realize I have to come to terms with my new "normal" and my current limitations. I can try to push, but I pay for it dearly. During the last months I was at work, I was miserable. I wouldn't accomplish much of my duties during the day while I was pushing myself to "be at work." I would then come home and quickly realize how much of a "mess" I was in as I would end up shaking, teeth chattering, nauseous, and crying because of the amount of pain I was now in merely due to the fact that I had gone to work that day...not even that I had done that much. Now, the mere act of dropping my daughter off at school can still be enough to set off an extreme bout of pain. Oftentimes, I will return home from dropping her off and it's as if all the nerves in my body are firing at once. (Have you ever had a migraine? You know the pain you get in your head at the slightest hint of light, sound, etc? Imagine that type of pain radiating throughout your entire body...not just certain points in your head!) There are still days I get to the point that I think I can't take it any more.

Admitting what I go through is still hard, and typing about it (both the physical act and the act of making my admission more public) is even worse. I hope just getting my thoughts out will help someone. At the very least, maybe this will offer at least a bit of catharsis.

This is all I can do for the day, but I will try to start posting more again, whether it's about my issues or something else.

Please let me know if this helps you. I'd also like for you to share in the comments if you experience similar symptoms, etc.

Monday, March 28, 2011

Randomness

Boy hate I steroids. I’ve had a lot on my mind lately, but taking a round of oral steroids just adds to the chatter in my head. The fact that I cannot focus on a single topic longer than a couple of minutes while they are in my system, added to the fact that it seems as if I can’t get my mind to shut-off, and throw-in all the things that have been on my mind lately…boy, that makes for some “fun.” Thus the title of this post… I just have to get some of my thoughts out, even though I know this will probably turn out to be a lot of disjointed, rambling thoughts; maybe it will give me some perspective on things at some point later on.
 
Location…location…location…

What’s more important – opportunities for your children or family? Is it more important to raise your children near family and build those close bonds or raise them in an area that you feel provides them with more opportunities? A couple of years ago, we were leaning towards opportunities, but now we’re changing our minds on that. We are starting to decide if there’s an area that might offer some middle-ground. We don’t like how we see certain communities taking a down-hill slide, but we think there are enough larger, surrounding communities that might still offer options, although none of the closer ones offer as many opportunities as we have available at our current location. Man, how I am praying we follow His will and guidance on this decision. I'm welcome to your thoughts and input. Maybe it will shed some light on an aspect we haven't focused on or an aspect we're struggling with.

Conception or adoption/foster

We know we want to welcome at least one more child into our home. Lately, it seems like God might be leading us into a ‘different’ direction. Besides our last pregnancy being considered high-risk, there are no signs to say that we could not conceive another child. However, for some reason, the ideas of foster care and adoption are staying at the front of our minds. 
Pure, unstained religion, according to God our Father, is to take care of orphans and widows when they suffer and to remain uncorrupted by this world. James 1:27 GWT

What are your thoughts on choosing to foster or adopt when you could still potentially conceive? It might just be out society, but it seems as if adoption is usually an option taken after one has exhausted efforts trying to conceive. That may be why it feels a little strange to be led down a different path. I’m still praying for God’s guidance on this to make sure we are listening to Him and following His will.

Family

Feeling the desire to be closer to family makes this next topic a little harder. Oh, how I want my daughter to grow-up near our extended families and have a very close relationship with them, just as I had when I was younger. However, there are certain things that aggravate me. You know those family members who always expect something? Ugh! My husband is still getting “guilt-trips” over the fact that we didn’t send anything back to our families for Christmas. Ok, excuse me, the end of last year was rough for us in more ways than one! I have my on-going health issues; plus, we started trying to live by more of a budget. I really wanted to send out a “family letter,” and I even bought all the stationary and hoped to get one created and mailed by year’s end. Needless-to-say, that didn’t happen. Now, all my husband hears is how upset they were because we didn’t send them anything for Christmas. That’s not the only incident of this ever occurring, either. More-and-more, it seems like all they are interested in is what we can do for them. I don’t mind trying to help out when we can, but when money, gifts, etc. are all that seem to be important to them, I start getting aggravated.

Tuesday, March 30, 2010

Chronic Pain

As I continue to struggle with pain, I'm also noticing changes in my attitude and behavior. It's amazing how much pain can changes one's life.

I'm finding that it's affecting my relationship with others, even beyond my interaction with my husband and daughter that I touched on in an earlier post. I wasn't very outgoing to begin with, but now I don't really want to go out in a group. I also don't want to carry on conversations with others; this one really bothers me, but I know where it stems from. Over the past year, especially with my husbands help, I've realized how often I say the wrong thing. This just adds another magnitude on to my ongoing struggle of not being able to remember common, simple words (like towel, dog, diaper, etc) from time-to-time. Who knows how many times I've misspoke at work or in some other situation where my husband wasn't even around to try to correct me. I hate it, and the really bad thing is that I've even noticed it starting to happen when I type, too. I now have to try to proofread anything I type at least a couple times, and there are still times when I send or post something just to realize that I typed something wrong at a later time. Also, I used to enjoy the fact that I my written word came out "more intelligent" than my spoken word…that's quickly becoming a thing of the past, too. Ugh! I really don't like this.

Ok, beyond noticing that I'm becoming a bit reclusive :o), I'm starting to get a temper and become very short with people…including my daughter. What?! I know she's just 17 months (today as a matter of fact), and I love observing her as she is learning from her surroundings. I also know that she gets frustrated easily because she can't communicate everything she wants to, and she can't do everything she wants to do either. Her frustrations combined with how short-fused I'm starting to be, especially on days that I'm really struggling, are not meshing very well right now. Take last night for example, I ended up so frustrated and mad at myself it wasn't funny. I was trying to feed Trinity supper. After a few bites of the mac-and-cheese I'd heated up for her she started getting antsy and wanting down. Because of how she'd been acting, I knew she was hungry so I kept trying to get her to eat. I was even letting her feed herself, which is her new favorite thing to do. When she started wiggling around, I started "helping" her with the spoon. Pretty soon, she was waving her free hand up and down at me. She pulled the hand with the spoon away from mine and flung it to the floor and then batted the bowl of mac-and-cheese down, too (not before sticking her whole hand in the middle of the food). Then she was really waiving her arms around, mac-and-cheese flying off her hand in the process. I ended up spanking her before I even caught myself. Yes, that ended her fit, but that's not what I should've done. After she quit crying and totally calmed down, I realized her "fit" was the only way she knew at the time to try to tell me she wanted something besides the mac-and-cheese. Why did I do that instead of taking the time to figure out why she was frustrated (which is what I normally do)? Like I said, I was very mad at myself for doing this. I was in tears last night, and I'm even starting to tear up as I write this now.

I so want to find something that will stop the pain I'm dealing with. I know other people suffer through even worse things, and I honestly think that may be why I'm still finding the strength to fight this every day. I just continue to try to thank God for the day He has given me and find blessings each day. But that still doesn't stop (or reverse) the changes I'm seeing in myself.

I'm really getting to the point where I just want to lock myself in a room on my really bad days. Even though, most days, I am so exhausted I just feel like I want to go to bed as soon as I put Trinity to bed, I really think I'm going to have to start doing more research into Fibromyalgia, Limited Scleroderma, and chronic pain on my own. Maybe, just maybe, I'll find something that might help.


Monday, March 29, 2010

Parenting with a Chronic Illness (like Fibromyalgia)

I had to repost this article from the National Fibromyalgia Association’s website:


FM in the Family
Reprinted from FMOnline


Chronic pain adds an extra challenge to every task, to every relationship, to every aspect of life—and parenting is no exception.

Recently we asked people with fibromyalgia to share their parenting tips. No request for tips has ever received such an enthusiastic response. Clearly, people with fibromyalgia understand that maintaining healthy relationships with their children is just as important as managing their symptoms—and they have plenty of advice for doing both successfully.

Here we present a selection of the best tips we received, hoping that they will be helpful to other parents with FM.

Time Management
Parenting requires so much energy—and people with FM are constantly focused on how to use their energy wisely, without draining themselves completely.

Chris Robbins, of West Bend, Wis., spent three years bedfast, fighting infections and fevers—and she had three children to take care of. Her solution: she taught the kids to set the kitchen timer for 15 minutes; when it rang, one child would come into Robbins’s bedroom to check on her (and, though they didn’t know it at the time, to give her a chance to check on them one at a time). When she had to get out of bed—to make a trip to the bathroom, for instance—she used that opportunity to teach a simple household task to one of her kids. “Soon, someone could cook eggs or macaroni and cheese. Another child learned to do laundry and another, how to vacuum and do dishes,” she says. “They started young and were proud of their accomplishments.”

Now the mother of two teens and a tween, Robbins has her kids well-trained to carry a cellphone and check in with her regularly—though not, she quips, every 15 minutes.

Making preparations in advance is a great way to keep stress levels down, and energy levels from dropping too fast. Try making school lunches the night before, and teach the kids to keep their backpacks near the front door—already packed with homework and textbooks—so that all of you can rush around less before heading to school in the morning.

Also, be sure to write your children’s commitments on a calendar, so you don’t have to worry that you’ve forgotten that PTA paper drive, that school dance, or that book report due date.

A kid’s schedule can sometimes be a boon to a parent with FM, as Leisa Ryan of Coral Springs, Fla., points out. “My advice for new mothers that suffer from fibro pain and symptoms is to nap when the baby naps—always,” she says.

Kathleen Kay Muir developed a unique system to explain to her family what kind of day she was having. She broke the day into a ratio of work time and rest time. A “50-50 day” was one in which she had to work and rest equal amounts of time. This helps the family understand how Muir feels better than if she simply said she was having a “good day” or a “bad day”—and it helps her teen daughter intuit whether she and Muir can go shopping or hiking, or if they will enjoy a “PJ day” of chick flicks. She has also explicitly told her family which tasks particularly strain her; when her husband and daughter take on those chores—like vacuuming and carrying in the dry cleaning—rather than Muir being stressed or frustrated by the chore, she feels grateful for her family’s willing teamwork. 

For Michelle Hock, spending time with her kids took priority over anything else. When they were little—they are now teenagers—that meant playing with them when they wanted to play, regardless of how much pain she was feeling. It also took priority over household tasks when her energy was at low ebb. “Don’t beat yourself up because the kitchen isn’t clean or the laundry is undone,” she says. “The kids only want their mom—and they want her to be happy, healthy and pain free just as much as you want to be.

“Take care of people first—things later.”

Take Advantage of Alternatives
We live in a technological society—and that can be a boon for parents who are experiencing an FM flare.

“I made sure I had every video available that they enjoyed—also, a remote-control VCR,” says Susan S. Muehlstein. “I taught them how to change the tapes. Timers on TV programs are also great!” She also relied on an alarm system that sounded off when someone opened a door or window; even if she was resting in a different room, she always knew if one of the kids went outside.

Remember that there is a lot of educational programming on TV—your kids don’t need to watch cartoons all day.

If volunteering in your child’s classroom is out of the question, seek out other ways you can be involved. Perhaps you can take on a small PTA project, be in charge of email reminders for your child’s sports team, or be on a planning committee.

Develop a Tool Kit
You may have special tools you use to make housework easier; why shouldn’t you use tools to make parenting tasks easier, too?

If your child plays sports, bring a cushion to make sitting on the bleachers less painful—or a light folding chair to sit on. If your children are infants and toddlers, keep a bag of supplies—diapers, wipes, nonperishable snacks, and whatever else you may need during an outing—in the car.

Communicating
Parents crave communication from their kids; parents with chronic illness need to make sure they are also sharing information with their children. “I try to let the kids know how much energy I have each day,” says Robbins. “It really helps what they will then ask of me or how they ask.”

Hock agrees. “Open communication about this is key, so the kids don’t think you are trying to avoid them or avoid being with them,” she says. “They are the most forgiving, understanding people on the planet; give them the chance to help you and love you through it.”

“I have a 4-year-old with a great imagination and energy level, and I have explained to her that I have a disease that some days makes me a bit sore and tired sometimes,” says Nancy in Pennsylvania. She also explained to her daughter some of the ways she is managing her symptoms, and bought a yoga tape the two of them can do together.

“The way I conduct myself with an adversity is the way she will see how to handle things that may come her way,” Nancy explains.

Cathy Stenger, who has a 13-year-old son and an 11-year-old daughter, is careful what she promises her children. “I never know what is going to come up that will use up my energy, so I find that in order to avoid disappointment, it's best not to promise something that I don't know for sure that I can follow through on,” she explains.

“My daughter knows that I have ‘an owie’ in my back and it hurts bad sometimes,” says Jennifer Betts, mother of a 3-year-old. “She shows true concern and helps me by picking up her own toys so I don't have to. Children understand a lot more than you think they do. And they love you unconditionally, despite your fibromyalgia.”

Tonya Walmer tried to prevent FM from affecting her children, despite knowing that was an impossible goal. With the help of a counselor, she came up with a way to offer age-appropriate explanations of her condition to her toddlers, who responded well. “That first conversation was amazingly helpful, but even more amazing has been the opportunity for openness and communication that it sparked,” she says. “Three years later, we have had many small conversations about life, the human body, FM, other disabilities, and even my children's own limitations. It has been truly incredible to discover that the very thing I was afraid to own is teaching my children—and myself—so many positive and wonderful things that serve them well now and will continue to influence them for the rest of their lives!”

One mom introduced her children to the world of FM a different way. “The best thing I have done was to encourage each teen that I could help them with a report or paper they had to write—if the topic could be on fibromyalgia!” Deb writes. “The end result was that they came out of it knowing all about the disease. Each of them came out with a greater understanding of why things were the way they were, why I reacted in certain ways, and how our lives were changed by the disease.”

No matter how carefully you explain FM, a sensitive child may react badly. One mom wrote us about her tween daughter’s excessive worrying; the girl is always checking on her mom, even when the mom says she feels fine. The two of them made an appointment with a therapist, who told the girl that she had to trust her mother when she said she was feeling fine—and trust that her mother would ask for help when it was needed. The therapist also emphasized that the child was not responsible for her mother’s health. “Although I have said those things many times, our daughter never really heard it until it came from a third party who she respects,” the mom wrote.

Be Child-Friendly
Keep in mind that your kids are a lot smaller than you are—but that doesn’t mean they can’t take on some responsibility, if you child-size it. Muehlstein used to keep small plastic cups in the lowest kitchen cabinets, so her kids could reach them to get themselves glasses of water; she also kept juice boxes and snacks on the bottom refrigerator shelves so the kids could serve themselves.

Tiffany Grimm, of Kenai, Alaska, has taken even more steps to allow her four-year-old son greater responsibility. “His clothes are in a cabinet that he can reach so he gets himself dressed,” she says. “There is also a hamper in his room for his clothes. It is small so he carries it to the laundry room on his own. As I am folding the clothes he puts away one stack at a time.”

Keep an eye on your medicines, too. Julie McCloskey, an attorney and a mother of two, keeps her prescription medications and herbal supplements in a locked safe, so the kids don’t have any opportunity to get into those bottles.

Younger children love to be picked up and carried around—something that can really exacerbate FM pain. A good option is to get down to the child’s level: play together on the floor, or snuggle together on the sofa. (A good stretching session before getting down on the floor may make playtime even easier on you.) 

Seek SupportMany parents reference a strong prayer life and spirituality as a way they manage their symptoms—and gain the strength they need to fulfill their parenting duties. Many are fortunate to have the support of their own parents, their spouses, and their children.

Whatever your situation, you must develop a system that allows you at least a little time to yourself, to relax, to meditate, to take a warm bath. If your budget allows it, you may choose to hire a babysitter once a month so you can have an afternoon all to yourself.

Part of a parent’s job is to set boundaries for the children—but parents with FM must also learn to set boundaries for themselves. “The very best thing that you can do for yourself is know your limits,” says Suzanne Stierwalt. “Know when and how to say no, and know when and how to ask for help.”

Walmer phrases it differently: “Put your oxygen mask on first,” she writes. Parents often instinctively consider their children’s needs first, but it’s important to maintain a balance. You can’t parent successfully if you are not meeting your own needs, and managing your FM symptoms. “If the balance is off too far in either direction, we are headed for crisis!” she says.

All in the Family
Is FM a genetic condition? That’s a hot topic in research right now, and the jury is still out on the extent to which genetics may influence whether a person develops FM. But what is inarguable is the fact that more and more kids are being diagnosed with fibromyalgia. What happens when a parent with FM has a child with fibromyalgia—and another without it?

“My 10-year-old girl has FM also and she has most of the symptoms that I have. I try to make it up to my 12-year-old girl, who is high energy, by doing things with her on my good days,” writes Shelly Tilley. “On my okay days, I do things with both of them, just keep it kind of low key. On my bad days, I cuddle up with the one with FM, and we make each other feel better just by knowing what the other is feeling. We do quiet things together, like reading, or watching a movie.  That's how I handle being a parent with FM.”

Carpe Diem
“Don’t let a day with your kids slip by,” advises Michelle Hock. “Do what you can do to be with them, pain or not; then rest later. The last thing you want to do is lose precious days with your kids due to this stupid, unnecessary illness.”

Remember that, while child-rearing can be stressful, it can also be joy-filled—and therapeutic in its own way. “My children have kept my spirits up and keep me very active, which is the most important thing right now,” says Juanita Martinez.

Seeking alternatives and creative solutions to parenting challenges can add up to wonderful memories for parents and children alike—and remember, the kid perspective is different from the adult perspective. “My kids remember the hardest times of my fibro (they were in their first years of school) as ‘the best times!’” says Muehlstein.

“For a while I felt like a failure as a mom because I hurt to much to take the kids to the park, play soccer, etc. One day my oldest son, when he was in first grade, said he felt so lucky because he had me around all the time,” recalls Mary Ross, who lives in Oregon. “This made my realize that while I couldn't necessarily be as physically active with my kids, I could still be a good parent for them.

“In fact, I think fibro has been a blessing in that it has forced me to slow down and truly get to know my children.”

“Be laid back,” Grimm adds. “They are kids. Their standards aren't high. It’s ours that are hard to meet!

“As a former child psychologist and teacher I would say it is most important to give your children their own responsibilities, help them understand and help, and be involved every way you can (even if that means watching a movie together or ordering the pizza for their friends).”

“We find small reasons to celebrate resting, or exercising to keep energy flowing,” writes Paige L. Koehler. She also makes sure to emphasize the things she can do, rather than the things she can't. “I couldn't carry my son—he was too heavy—but I used a wagon and stroller quite a bit,” she says. “I had to stop bowling, but I could still walk. I had to quit chopping and cutting food but I could still supervise a small cooking group with the family. 

“Find the fun, and you will do fine.”