Monday, January 27, 2014

What have you been up to?

It has been freezing here on the East Coast so we have had to find ways to keep busy.  Painting the kitchen, making placemats,  and rice crispy treats! Wondering how everyone else is enjoying your time indoors?



Wednesday, January 8, 2014

Brrr baby its cold outside

Yesterday was the coldest day in history for Maryland or at least the last 20 years. The pipes at work burst yesterday and today we went in there was no heat. So here I am at home getting paid and doing chores. What a way to start the new year. Almost all of the Christmas decorations are down. I need to get a new wreath for spring so I can take down my Christmas wreath. I love the cold but this is crazy...anyone else ready for spring?

Wednesday, January 1, 2014

Bring it on 2014

2013 in review was a great year. Started out a little bumpy but quickly corrected itself.  After saying goodbye to dear friends and starting to rebuild in a new house I can say all is good. This year my husband gave up his dream job to be more available and to spend more time with Jackson and me. My baby turned one !  He is so big and amazing.  We welcomed in a new family member in June. My brother is so happy and for that I am glad.  My baby brother is all grown up. I love seeing them so happy and healthy.  lt means the world to me to be close to my parents. I will be 30 in 2014 but I still need my Mom and Dad. This year Lupus gave me a break about half way through.  And for that I am thankful.  Going into 2014 we still have Some residual issues like the leaky roof / wet chimney and less than optimal A/ C but those things will work themselves out. This year I say goodbye to my 20's and I am ready. I want to give back.I want to spend every spare minute remembering the good times and dreaming of the better ones to come.  This year I am going to focus on the good.

Sunday, December 15, 2013

No one shares the good days

I have been feeling so good for such a long time that I have neglected to keep up with my blog. That is a huge mistake. I am sorry. People with lupus need to hear about the good days as much or more than they need to hear about the bad days.  My time has been filled with holiday gatherings that were missed while we were in Texas. Now that we are home each weekend is full of family activities. We have already had a few snow days which really let you know Christmas is right around the corner.  I am trying to stay healthy and keep the stress under control.  Even though I am being tested with the new roof and chimney repairs that did not seem to fix the leaks.

Jackson is getting so big. He says so many words...his favorites are dog, truck, and no! This year I am excited for him to open presents and see Santa.  It is crazy how different this year is from last.  I miss my Texas friends like crazy especially around the holidays.  I can never express how much they mean ro me and my husband.  They are family.  I couldn't have gotten through last Christmas without them.

I am blessed.

Monday, August 19, 2013

Beach Beauty with Lupus

It ha been a long time.  Apparently I only enjoy sharing my journey with Lupus when something bad is happening to me.  Since it's been so long since I've felt really crappy I haven't felt the need to share and that isn't right.  People need to know that there are good days, even great days!  Days when you forget you have Lupus.  I went to the beach and for more than a quick ten minute "I saw the water" and I'm out of there!  We spent hours playing in the sand, touching the water with our toes and napping all under the protection of a bunch of umbrellas, hats, and lots of sunblock!  For Jackson, it was his first trip to the beach.  For me, it was my first trip to the beach with Lupus.  Although I will say it was not incredibly awesome wearing so much protective wear I didn't feel too out of place.  No one that I noticed was staring at me or acting like it was odd that I wasn't sporting a bathing suit like everyone else.  I think the push nationally for SPF is helping.  They are making some very cute SPF clothing and everyone is well aware of the risks of the sun!  My family helped a lot too!  Always reminding me to move my chair so I stayed in the shade or asking if I needed more sunblock.  I am grateful for the vacation to feel normal.  I am so proud to say I didn't get the slightest bit of sunburn.  I came home the way I left, no aches and pains.  Getting enough sleep on the other hand was a challenge!  Jackson is 16 months and in the 98th percentile for height and weight.  So need less to say he did not want to sleep in his pack n play.  We alternated from the floor to the futon to the bed and no one slept well in his room since he snores and breathe loudly all night!  So, its back to work and daycare.  Back to waiting for the next big thing!  We do not have another vacation planned yet but I am excited thinking about all the places I want to take Jackson that for a long time I didn't think I was going to be able to. 
Jackson and I enjoying the beach for the 1st time!
 
If you have time, please check out this link to see my team in the Walk to End Lupus Now Maryland walk which is in 40 days!  I would love to have you on my team or as a supporter.  Lupus is a horrible disease that hurts so many people.  I am blessed with a wonderful support system and the best doctors in the country.  I know times are rough for everyone but if you can afford $5, $10, $15 please consider a small donation to my cause.  I will not stop asking until we find a cure.  I appreciate everything you have done, are doing right now, and will do in the future to support my family and myself in this crazy journey.

http://lupusdmv.kintera.org/faf/search/searchTeamPart.asp?ievent=1072113&lis=0&kntae1072113=F6592DC0DFB442169501F5E3EA263764&supId=0&team=5526234&cj=Y

Wednesday, June 12, 2013

Want to learn more about Lupus?

26th Annual MD Lupus Summit

This is the link to the summit.  My husband and I will be attending this year.  It will be hosted at Johns Hopkins University and it is a free event.  If you are a new lupie or know and love one this is the event for you.  Word on the Lupus street is that Dr. Petri of the Lupus Center at JHU, my doctor, will be the keynote speaker.  Hope to see you there!

Tuesday, June 11, 2013

Now I Am THAT Parent...

Who gets into fights in the daycare parking lot.  Yup, that's me.  I knew it was going to happen and I expected it; however, I never expected this to happen in the parking lot at my son's daycare.  But I guess I was wrong to think that the nerdy old man who was exiting the daycare center would just smile and nod like the nice old man he appeared to be.  Oh boy was I wrong.  This week my arms, wrists and hands are sore and have been on and off numb.  So, even though my knees have only been hurting on and off, I pulled into the handicap spot up front and pull my handicap hang tag on my rear-view mirror.  I got out of the car and headed toward the door minding my own business.  I passed the old man with his child or grandchild and it took me a minute to realize what was happening.  His young son was talking about something but this man was talking loud over his son apparently not paying one bit of attention to what the child was saying.  What was this man going on about?  I only caught bit and pieces but the general idea was "There goes another Marylanders wrongfully parking in a handicap spot but is perfectly healthy, its a damn shame, blah blah blah" I couldn't believe this was happening and I planned to just be the bigger person and keep walking but I could not do that so of course I spoke up.  I turned around on my heels and said loud enough so he could hear me "Sir, you are so wrong and in fact very rude.  Not that I have to explain to you but I was issued this pass by the State of Maryland, you do not know me and I do not appreciate your accusations.  This must have caught him off guard because he began yelling about how he hates this state that gives everyone handicap tags and how it is misused and abused by people like me.  At this point I had to choose between continuing to argue with this man or to go inside, which is what I did.  I reported him to the front office, which has a window so the ladies could see who I was talking about.  There were two ladies, one laughed when I said "That man was harassing me in the parking lot and I do not appreciate it, he is very rude."  I looked at the woman who was laughing and said this is not funny.  Boy did that wipe the smile off her face.  I can only assume she was laughing because he is a problem father but I do not have anything to confirm that.  I surely hope she wasn't laughing because I said he was harassing me.  I told the ladies that he was yelling about me parking in a handicap spot and that I actually do have a legal pass to do so.

When my husband and I attended the first Lupus group meeting back in San Antonio, TX, the group leader said she was confronted at a store once by a man who started banging on the handicap parking sign saying she shouldn't park there since she is not disabled.  People are so insensitive and rude.  Not everyone who has a handicap or disability uses a wheelchair or crutches or is missing a leg.  To assume that someone with a handicap tag is lying is absurd. If they have a problem with who the DMV provides passes for then they should take it up with the DMV or their representatives.  I do not regularly use my pass but if I did it is no one's business.

I have lupus but I look fine.  My joints are stiff and throbbing but you don't see that. I hope I do not run into this man in the future.  I hope he was picking up his child at that time which was not a normal pick up time for him.  What should I do next time, smile and wave?  Ignore him?  I do not generally believe saying nothing is being a bigger person.  A bigger person stands up for whats right.  As a new member to the lupus community, it is my job and responsibility to point out assholes like this man and let them know how wrong they are.

I sure hope his child does not grow up to be like him.  Maybe he will be more compassionate.  I hope this evil man gets a horrible disease like Lupus and can't walk but still looks normal and healthy.  I hope someone calls him out on this when he parks in a handicap spot and I hope he remembers what he did to me.

Jackson and me celebrating summer finally!