I am currently on vacation in Tennessee visiting family. It is a welcome reprieve form life and the stresses in it. We have not had a true vacation in five or more years. This spring break for my girls is their first since entering the public school system. It is exciting to see their minds to take a break and I admire, and am so proud, of how smart they are becoming.
One issue I am having with this vacation is me. I am finding myself not being able to do the activities with others. I am in constant need of more breaks and rest stops. Some times I just need to stop and sit for 20 minutes as my energy levels are too low.
Chronic fatigue hurts.
This coupled with the pain I am constantly in makes it difficult to enjoy some of the exciting aspects of my vacation. I am having to accept the fact that I have more limitations on what I can do. This hurts more than I first anticipated.
Yesterday I went to a children’s arcade/play place with my two eldest daughters and my nephew. My girls had a blast running around in the playground area and climbing the inflatables. They wanted “dad” to run and jump and play. I smiled and did my best, but no where near what I felt I should be doing. It hurt me to tears and not being able to play with my girls.
Today we went shopping. I was the only dad in the group of 6 girls so I ended up with both shopping carts and helped with the lifting and sorting. It was a morning that was already rough due to a fibromyalgia flare up. I ended up sitting more often than not. I smiled a fake smile and pushed as hard as I could through the pain. It wasn’t enough and I felt terrible. I felt guilty at holding the group back, even though I knew I could do nothing about it.
It is a hard situation in the fact that I am suffering from a chronic illness, feeling that I am letting my family down by not keeping up, and then having the guilt and depression from all of it. Constant 24 hour pain and having some seasonal allergies pop up complete the horrid picture. I feel so tired of fighting.
And its not just the chronic fatigue.
I have been reviewing my condition and well-being these past few months. I have looked at my medication and doses and have decided that i am in need of an increase. I have been reviewing how much I have limited myself in lowering my dosage to not have to deal with the pending opioid crisis. I have talked with my doctors at lower it so I am not considered in the “addict” category. I am slowly realizing that this is futile and I need to focus more on making sure that my needs are met.
Then there is the guilt from others at taking a vacation.
Society seems to think that a disabled person is someone in a wheelchair or crutches, barely able to move ever. I have received, for lack of a better word, hate for doing activities that I love that I should not “be able to do” because of my condition. Just because I suffer does not mean that I cannot take a vacation. Do we give up our right to happiness by having a condition that holds us back? This does not mean I get to take a break from my illness. I have suffered everyday of my vacation. I do not get a break from my symptoms. Why must I suffer the feelings of others who feel the need to tell me that I must be faking if I go on vacation. Why add that to someone who is already suffering?
It feels incredibly frustrating.
We try to live normal lives. We deserve to have vacations and enjoy life when and where we can just like everyone else.
3 thoughts on “A Vacation, Part 1”
I totally empathize with you Daniel. You are NOT alone in the fight…you are loved and cared about every day!! I am Rachel’s Mother and I understand….keep your eyes on the positive and there is some each and every day. Don’t focus on Negative People…..they don’t really understand and actually lack compassion for anyone but themselves. Remember you are loved every day and cared about ❤
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Thank you so much Mrs Ochs, I know who you are. You have an amazing daughter who fights so hard everyday. Thank you for your kind words.
BTW Daniel…Everyone should take a Vacation. You deserve it and the wonderful therapy from taking one cannot be measured. If I could I would be on Permanent Vacation! Maybe that will happen sooner than I think 🙂 Also it is a very helpless feeling to have a child that is a “fighter” like you are and not know how to help or what to do to ease their condition for them…things we have to deal with in our lives here on earth will one day all be removed ❤
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