And I had to go all manager-style and put the kabosh on that for safety reasons.
I woke up, screaming at him.
And, I woke up screaming.
Recently we saw a conversation among several friends in our Facebook group about how under appreciated many of the wives feel as caregivers. At the bottom of it is that most of the women feel overwhelmed. Here's what they shared and things husbands should keep in mind.
Several of the wives juggle the demands of parenting, homemaking, and a job. On top of that they all--to some extent--take care of their spouse's disability-related needs. Typical tasks include dressing, exercise, bathroom care, feeding or preparing meals, medicine, doctor and therapy appointments, cleaning up accidents or wheelchair tracks, and a dozen or more others. By the time they get to bed they're exhausted. However, if their husband needs anything during the night they're still on call. It is never-ending.
Many of them understand that their husbands generally do what they can to help. These guys range in physical ability and time after injury. But many of them aren't necessarily angry with their husband.
This reminds me of a point Dana and I have made time and time again: the disability and all of the stuff that goes with it is a third person in our marriage. It helps us focus our frustration away from each other.
That said, beyond what husbands can do for our wives is what we say to our wives. Overwhelmingly, the wives said it means so much when husbands say "I love you" and "Thank you." Such a simple, but thoughtful step lightens their burden. I find Dana really appreciates when I ask her--not order her--to do something. Finally, the wives mentioned how important compliments and gratitude for the non-caregiver things are; that they like to be reminded she is your wife first.
It's so good to know this isn't rocket science. While compliments and affectionate words won't always trump the overwhelming waves of caregiving, they help fill the sails that keep our wives going.
Thank you for contacting us and for your concern about the stem cells. There are no proven treatments utilizing any kind of stem cell so far and as you know there are several experimental “treatments” being introduced for purchase without a valid clinical trial program being completed, leaving their safety and efficacy untested. This is a great concern to researchers, clinicians, and most importantly people with paralysis. It is unethical to charge people money for unproven medical treatments. It is important to remind your friend that any cells that are put into your her can never be removed and it will exclude her from participating in valid clinical trials.Another important point from her response:
There are three main reasons why a person might feel better that are unrelated to the actual stem cell treatment: the “placebo effect”, accompanying treatments, and natural fluctuations of the disease or condition. The intense desire or belief that a treatment will work can cause a person to feel like it has and to even experience positive physical changes, such as improved movement or less pain. This phenomenon is called the placebo effect. Even having a positive conversation with a doctor can cause a person to feel improvement. Likewise, other techniques offered along with stem cell treatment—such as changes to diet, relaxation, physical therapy, medication, etc.—may make a person feel better in a way that is unrelated to the stem cells. Also, the severity of symptoms of many conditions can change over time, resulting in either temporary improvement or decline, which can complicate the interpretation of the effectiveness of treatments. These factors are so widespread that without testing in a controlled clinical study, where a group that receives a treatment is carefully compared against a group that does not receive this treatment, it is very difficult to determine the real effect of any therapy. Be wary of clinics that measure or advertise their results primarily through patient testimonials.These are extremely important points we need to understand and educate our peers on.
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