Today is the day I switched back to Wahls Paleo level II. I’ll go back to level III when I am in a more flexible situation. Talking about tackling the Wahls Protocol with limited funds may be an unpopular or uncomfortable topic, however it is a very real problem that others wishing to transform their lives with the Protocol will need to face who have the same issues. Many people who have this illness and other devastating autoimmune illnesses are disabled. I don’t have to be a genius to figure out that there is more poverty among the sick than the well. My goal is to get through this first year on a limited income so that I can devote all my energy to rehabilitation, then start working full time. Some of my blogs are going to be about that struggle. It is a real one, it is a difficult one and it will be ongoing. It requires a great deal of juggling, problem solving, creative thinking and constant sourcing. It forces me to pick and choose what I can do and what I can’t according to what is most beneficial because of lack of funds. As I find answers and ways around this problem, I’ll document everything I learn. Maybe I can make it easier on the next person. I’d like to think so.
I don’t speak of this to discourage anyone from trying who may be facing limited means. Instead, I hope to prove its possible, though not easy. My health is leagues better from when I began. So much so, that I can’t wait to go to the Calgary Zoo in the spring. The Zoo has been an annual gauge of how much sicker I was from the year before. I didn’t bother trying last year and the year before was horrible. I spent most of the visit sitting it out in the air conditioned Cafeteria completely fatigued even though I had a rented motorized scooter.
The Protocol is a carrot worth fighting for. It is not elusive and it pays off every single day. That pay off is what makes it possible to stick with this, because it works and is doing the formerly impossible. That is what fuels my resolve to stick with it. So, I will continue to juggle, problem solve, research and source. It is a huge mistake if I start working now, I know that and it goes against the original blue print of beginning work after one year on the Protocol. If I work before I am ready, I can and probably will jeopardize everything I’ve worked so hard for this year by piling on a complicated schedule making it impossible for me to rehabilitate, keep appointments, exercise and take the time needed to prepare the foods I need. Whereas in five months, I should be finished with all rehabilitation appointments, not including exercise, which is the same as breathing oxygen. I will have five more months to gain strength and heal. I will have had career counseling with employment offices, counseling with a MS psychiatrist and MS social workers who will help assess my skills versus my physical disabilities thus insuring the best possible chance for a successful shot at returning to work and having the ability to continue to follow the Protocol faithfully.
At the end of this, it may be prudent to have to stay on disability and work part time. I have to be prepared for that possibility too. However, I listen to people going to back to work because of their own incredible healing online, but all of them have a second paycheck in the house to back them up. I’d love to speak with someone in the same vulnerable situation I am in that has successfully gone back to work after years on disability without a second income backing them up. That is another good reason to document all this, so that future people in my shoes, who may trip across this blog, will have me to be inspired by. In the mean time, this is a pep talk for me.
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