Thank You to 3sistersabroad.wordpress.com
For the nomonation, Im honored
Now for your questions and answers
1 What inspired you to blog? I have several conditions that cause chronic pain. I want to inspire others that feel they have no answers to their many questions
2 Where did your blog name come from? I am grateful for the ups and downs in life as they are all things i can do to inspire and educate others and having chronic pain~ ChronicallyGrateful and My Name is Deborah L Andio (Debla) = ChronicallyGratefulDebla
3 Whats your favorite food of all time.
I love Mexican food the spicer the better
4. If you won a million dollars what would you do? Spend it, travel, save? All of the above First I would pay off all bills buy a cute 2 bed 2 bath home in Florida, pay for my granddaughters college education,pay off my daughters house,take my entire family on a trip to Croatia for a week then to Italy for 3 days and Holland for 3 days then I would donate 50.000 usd to my church 50.000usd then 50.000 nonf.org and 20.000usd to a local mission, foodbank and domestic violence shelter.
5. If you could live anywhere in the world where would it be?
Hmm thats tough. In the USA it would be Florida and worldwide my choice would be Croatia, maybe if I will that million $ I can buy a small villa in Croatia
6. If you were granted 3 wishes what would they be?
1. All diseases would be cured
2. People could learn to live as one human race instead of all the violence we see in this world
3. That noone would ever go hungry in this world
Now I would like to nominate……drum roll please…
* Thank the person that nominated you and leave a link to their blog
* Post about the award
* Answer 6 questions about you.
* Nominate at most 7 other people
* Tell your nominees the good news.
Your Questions Are
1 How did you come up with your blog name?
2. What inspires you?
3. Why did you decide to blog?
4. If you could have one super power what would it be and why. ?
5. If you had 3 wishes what would they be?
6. What is your favorite food?
Avascular Necrosis/Osteonecrosis falls under rare disease
Support Group For Avascular Necrosis/Osteonecrosis
Faithful Friday! From Stressed to Blessed
Ways to take care of you
Keep showing up and you will see and feel a difference in your life
For 30 days
Things you complain about stop.
How to flip the negatives
1 don’t get paid enough: Instead thank god your working
2 I’m gaining weight : Instead put yourself on notice you will eat healthier. Just Look how beautiful you are.
3 My bones hurt : Instead say I am so glad I am alive to live and feel another day.
Be Grateful for everything!
When we get on social media post something we’re grateful for everyday!
Week One. Gratitude
Week Two. Detox your environment
Week Three. Spiritual detox. Replace 30 minutes if tech time with a simple act of kindness
Week Four: Work on your Temple. We fuel our soul let’s not forget to honor & take care of the temple
Stay tuned for more!!
Being diagnosed with a chronic illness-condition- disorder such as osteonecrosis, hashimoto and osteoarthritis or any other illness can come as a hard blow. And being grateful when your suffering with pain is hard. But we have to stop and think and reflect and be grateful. We have so much to be thankful for.
Our Family , Friends, Support Groups and more….like the beauty of a new day or an amazing sunset…
We lose our-self in pain some days …. and If you don’t have the condition or disease you don’t know what that person goes through…
We hear …..Keep your head up – It will be ok …. it cannot be that bad….that gets so tiring especially coming from those who don’t know what its like…..doctors do it, family does it friends and its just exhausting trying to stay strong when your falling apart.
It’s normal to experience a range of emotions in the wake of such a diagnosis. However, you can learn to manage these feelings to live a fulfilling life.
Trying to absorb the news of your disease can bring a flood of emotions. A diagnosis of say Osteonecrosis leaves you in shock, frustrated as many Drs really don’t understand the disease or all its known and unknown causes.
Grief is another common reaction to chronic illness. You may experience various stages of grief including denial, bargaining, anger and sadness.
You may feel you’re on a roller coaster of emotions accepting one day, and angry the next.
It may help to remind yourself that these feelings are normal, and will likely ease with time.
Some days you may be tempted to just pretend you never received your diagnosis and act like all is well However, facing your diagnosis head on is the best way to cope.
How can you actively face your disease or illness? A good place to start is by writing down all of your questions and taking them to your physician to discuss. Ask your doctor what specific steps you can take to optimize your health. Accurate knowledge can help you feel empowered.
Song Of The Day
Also try to manage the things in your life that are within your control. You may not be able to control certain aspects of your disease, but you can choose to eat healthy meals, take medications as prescribed and spend less time with people who aren’t supportive.
Also it’s a a good idea to minimize some stress by letting go of unnecessary obligations. You may be able to take time off from volunteer commitments, for instance, or ask for more help from family and friends. Get into a good strong support network you can rely on, and communicate with them about how they can best help you manage your pain and coping with your disease.
Illness and disease can be stressful for an entire family. Patients don’t want to be “difficult” but we get do tired of explaining we just give up trying to tell you whats wrong .
Thats why we have support groups….and I am so grateful I started on.
I hope to help others and they help me as well.
Although support and self-help groups can vary greatly, all groups share one thing in common—they are places where people can share personal stories, express emotions, and be heard in an atmosphere of acceptance, understanding, and encouragement. Participants share information and resources. By helping others, people in a support group strengthen and empower themselves.”
If you have Osteonecrosis and need a support group we are here Avascular Necrosis/Osteonecrosis Support Int’l
Chronic Conditions Can Take A Toll On Family
It’s not unusual for couples to experience some strain on their relationship. After all disease and illness effects the family.
Try to see things from the other’s perspective.
Also encourage the caregiver if you need one to take some time for themselves .
Having a chronic, illness or rare disease can disrupt your life in many ways.
You may often be tired and in pain.
Your illness might affect your appearance or your physical abilities and independence. You may not be able to work, causing financial problems.
Support groups might help, too. You will find that you are not alone, and you may learn some new tips on how to cope.
Try to find small things that you can enjoy every day, and set realistic short-term goals for yourself. Even small goals such as a visit to a park or museum, you don’t want to shelter yourself.
You have to stay focused on the positive happy things in your life.
Be grateful for small things, good days, I never try to dwell on any pain I’m having to much
I try to be grateful for everything as the mind set is half the battle.
Stupid little things that used to upset me or tick me off , I now laugh about.
I am blessed with a wonderful kind considerate hardworking husband, I can honestly say we rarely argue. And when we do it lasts all of maybe 5 minutes, then we look at each-other and start laughing
We both know after being together over 20 years that arguing doesn’t do anything positive.
I’m sure there are days I drive him crazy and vice versa, but we’re both grateful for each other and we know we will get through anything together.
Every day we say I love you. Everyday we show our love for each other in some small way.
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All files, art , logos and information contained in this Website or Blog are copyright by Deborah L Andio ©Debla2016 ,copyright , all stories, writings art logos are my own and may not be duplicated, copied, modified or adapted, in any way without my written permission.