2012 Resolutions
I finally achieved my previous years resolutions. Remember those? When I was pregnant and cranky and not too interested in self improvement?
Here they are:
1. I will gain 20 pounds this year.
2. I will have a baby in the Spring.
3. I will attempt to lose 30+ pounds and probably quit about ten pounds from my goal.
4. I will begin an exercise program.
5. I will try to accept that my life might not be perfect now, but it is still really damn good.
6. I will not try to stop swearing.
Yup, I did them all. I exercised great for about two months and then it got cold and I quit. But, my resolution said I would start an exercise program, not that I would continue to exercise. And I tried to lose 30 pounds, and then quit 30 pounds from my goal. See? I totally nailed it.
So, this year I am setting some actual goals. This is what I've come up with so far:
1. Read scriptures and pray as a family EVERY NIGHT. Because we are awful at this.
2. Lose weight... I'm not picking a number like I normally do, because this year is going to sort of turn my life on its head and I don't know how I will be feeling. But, lose as much weight as I can, exercise as often as I feel able, and stop eating sugar. For the tenth time.
3. If I feel capable, run in some sort of a race. It can be a 5K, even. Eventually, I would like to run a half marathon, but I don't know if I will get that far this year.
4. Have Lizzy and Bennet start doing their own laundry.
5. Say "You're welcome." instead of "No problem!". I've learned that "no problem" bugs people, and I do it without even thinking. So, this is my attempt to be less annoying, I guess.
6. Practice the piano 30 minutes a day (if possible) and learn to play at least 100 hymns in the hymnal.
7. Be cured.*
*More on this later. This would be the Life Changer. I believe (and am waiting to confirm the diagnosis with blood tests. Should have the results within a month.) that I was misdiagnosed with MS. I am almost positive that I have late stage Lyme Disease, which can be hard to cure, and the treatment can be excruciating. But, it is curable. Sometimes it takes years, though, so I guess we'll see how it goes.
Still, there is a cure. And if any of you have MS or any autoimmune disease, I would strongly encourage you to find a doctor that is well-versed in Lyme disease. Almost everyone with Lyme gets misdiagnosed with something else first. Rheumatoid arthritis, ALS, MS, Parkinson's, lupus, Alzheimers, etc. etc. etc.
Or go here. That site says that a clinical diagnosis for Lyme can be made if the patient has more than 20 of those symptoms. I have 43. Go check it out. Pleeeeease check it out. My neurologists blew off the possibility of Lyme. "There is no Lyme disease in Washington state." First of all, yeah there is. And even after they learned I lived in Pennsylvania 16 years ago, they still told me it wasn't Lyme.
EVEN if you have had a negative blood test, you might still have Lyme. There is no accurate blood test for it yet. Patients that have been bitten by a tick and then got a bullseye rash have still tested negative for Lyme. (And in case you don't know, if you get a bullseye rash, you have Lyme disease... end of story.)
Anyway, sorry for the Lyme disease rant. I have been reading about it nonstop and it is freakin' me completely out. People are dying from this disease because doctors have diagnosed them with other neurological disorders. Most doctors don't know enough about Lyme. Nobody should have to die from this. Watch "Under Our Skin" on Netflix to learn more.
Okay, okay... I will shut up now. If you have any questions, leave a comment or email me at maryspemberley at gmail.com.
Here's to the New Year!

:( Not that I hope it's the latter, but it's certainly better than the former. Urg.
i hope you have lyme and not MS. That would be great! Owen had lyme. Of course where did he get it? PA! He had the bulls eye rash and was very ill. Since you've done the research, do we need to be worried about it since it was so long ago, and he has been fine since he was treated? He was SICK! down in bed with fevers! Very sick!
I love reading your blog. A former teacher of mine went to Brazil to be a missionary and came back with Lyme. It took close to 10 years before he got an accurate diagnosis. Good luck!
Holly, how long was he on antibiotics? He is probably fine. When you catch it early, it is easily treatable. HOWEVER, if he ever starts having neurologic symptoms or arthritis... He should see a LLMD right away. (Lyme literate MD).
Wow. My mind is spinning. I was told the same thing... no lyme in Utah. hhhhmmmmmm..... I must research. Thank you for sharing.
Be careful mary. I went down this road BEFORE my diagnosis of MS. I don't know if I ever had Lyme or not, I went to a LLMD and the treatment just about killed me. I completed treatment 5 years ago and still have side effects from the medications. I truly believe I am worse off now than before treatment. Sorry, I don't mean to be pessimistic, just want you to see my angle. I know there are some great positive stories as well but the 3 people I know personally from my treatment center (and still have contact with) ALL are worse now after treatment. You can email me if you want further details or have any questions for me. I did always laugh at the doctors who think there is no Lyme disease outside of the northeast, like there is tick border control or something. Lyme disease is everywhere.
I wish you the best Mary, be careful and I will keep you in my prayers.
I am praying for discernment and thorough caregivers for you, Mary. Have you read this blog >http://mabelshouse.blogspot.com/ ?
She had a nasty case of Lyme disease. Perhaps she can offer some insight or support? Blessings to you.
Great goals and I hope you get some answers soon. Crossing my fingers it's treatable!
Owen was on abx for about a month and a half. I think he was treated pretty early and so far no neuro probs. btw, Maggie was looking at the pic above on the top of your blog, and she saw Mckay with all the kids and she said, "is she a single mom?" I guess she looks a little older than Maggie thought. I had a good chuckle.
Oh my. I got 37 on the test. I have been diagnosed with fibromyalgia. Do you really think Lyme disease is missed that often? I guess I had better watch the movie you recommended.
I sincerely hope yours is Lyme and not MS.
I totally agree with you! A few years ago I was having a bunch of neuro symptoms and asked my doctor about Lyme Disease and he said "you don't look like the type who goes hiking in the woods a lot"....but as a teenager we lived in the woods pretty much! So who knows but I hope you get a good answer!
Miranova, I will email you.
Kim, I had read her blog a few times in the fall while she was dealing with dizziness. How long ago did she have Lyme?
Anonymous, yes, I really do think Lyme is missed ALL THE TIME.
Mary, I have a friend who has dealt with Lyme disease in both herself and her children for YEARS. If you'd like, I can put you in touch with her. My email addy is claireboe@gmail.com.
Mary, I just want you to know that I am praying for you.
Debbie from Illinois
I watched that documentary and it was terrifying and so sad. I wish Lyme was better diagnosed and treated.
Are there any other tests beside the standard blood test a primary doc does? I have been diagnoses with Fibro but have always wondered. I've had two basic blood tests and Lyme was negative. Just wondered if there was more testing that could be done to rule out. Mary I will be paying that whatever the outcome that you can get treatment and relief,.
Seeter, the test doctors use most often is called the ELISA test and it gives false negatives all the time. I have had that test and was told I don't have Lyme by my neurologist. The most accurate test is the Western blot, but It is expensive and insurance doesn't cover it. ($400). It still gives false negatives a lot... I've heard as often as 50% of the time. that is why some doctors will make a clInical diagnosis of Lyme if a patient has enough of the symptoms.
I am waiting for my Western blot results, but won't get them back until the beginning of February.
I'm obviously not a doctor but it seems that if it gives a false negative so often why not just treat for Lyme to rule it out. I mean I know it's not good to hand out antibiotics for every little thing, but if a patient presents with symptoms why not just treat before assuming something much worse. In my case there is no cure and really no treatment. Most meds don't help with the pain and you can forget the other symptoms. If you treat me for Lyme and it's not it then we can move on. Especially if Lyme can progress much worse over time. But what do I know I guess. Wishing you much luck
as a nurse (and paranoid mother) i knew about lyme disease, but i had no idea that the testing was so inconclusive or unreliable. how frustrating!!! i watched the documentary and have told others about it. i hope and pray that you get the answers you need to get the right treatment. xo
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