My wife has come down with a sickness and had to stop working. The doctors won't officially tell us it's MS but are telling us it is MS. I've got good insurance through work but it doesn't cover some of the special test to confirm until we've paid out almost 10 grand. Without those test she can't get disability either. With her out of work the last 6 months it's drained our savings. If anyone can help or has advice we'd appreciate it. As it stands after cutting everything out that we can and selling everything we don't need we will still come up short about 700 a month until she can get disability or go back to work. This is mainly just me needing to scream into the eather in frustration, but if anyone has advice or prayers we would appreciate them.
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Prayers just went up. Have you watched this documentary?
https://theuniversalantidote.com/
Apparently facebook (if ur on it) has many sites full of healing testimonies re: chlorine dioxide (MMS or Miracle Mineral Solution). Including “incurable” diseases.
Also FloridaSharkman on TS might have a solution for you. He’s very responsive to questions.
I’m sure others here will have good suggestions.
Hang in there…
Thx
I've prayed for you fren. I'm sorry to hear about your wife and I hope you can get a definitive diagnosis soon so you know what you're dealing with. I wouldn't be surprised if some frens here post about treatment protocols.
As for your financial situation, I honestly don't know what to tell you. I know it's not ideal, but perhaps consider some type of go-fund me campaign to pay the doctor's bills until you get that outrageous deductible paid. Other than that - perhaps taking on a second job temporarily? Maybe doing customer service phone work from home? Perhaps that's something even she could do? If you both did it, it probably wouldn't take too many hours per week to make up that shortfall.
I have asked God to guide you and enlighten you on options and to give you a sense of peace that He is with you through this trial. I wish you all the best.
Thx
So sorry to hear about your wife's problem.
Before you start down an expensive (and possibly toxic) road with Big Medicine, it might be worth looking into supplements and lifestyle changes that could help. Below is the Protocol page for MS at Life Extension, and I've pasted in a short list of supplements they recommend for MS patients. Millions of people WITHOUT MS (including me) take all these and more, and they're generally beneficial for anyone, so I wouldn't wait for a confirmed diagnoses to consider starting these.
Also, there is a LOT more available out there; dig in and do some research and you might find enough help that bankrupting yourself for medical care isn't needed in this case. Worth a try, I'd think.
Best wishes --
https://www.lifeextension.com/protocols/neurological/multiple-sclerosis#
Lots to look into. Thx
Sending prayers for sure❤️🙏
Thx
Dear Jesus,
We thank you for your mercy and loving-kindness. You see this situation and You are able and willing to heal this lady and solve the financial issues that are causing stress in this home. May Your will be done and may all those concerned give You the honor and the glory that You deserve. Amen
Thx
Start a gofundme and post the link on this site.
Was told that was against the rules.
Go and research the carnivore diet. I have a friend with MS and she has NEVER REPEAT NEVER taken any of the medication. Only high dose Vitamin D3/K2 with FAT. It is a neurological disease. Nerves are made of Fat and Protein …..No carbs. See Dr Shawn Baker, Dr Ken Berry and Dr Anthony Chaffee. See also Homestead How. All have thrived on meat based diet and many have cured disease including MS and you will not hear it from our lively medical community. Only caution go at her pace if overly tired after a few days of very low carb - add plenty of salt and iodine drops (Dr Ken Berry) Good luck and God bless do not let them panic you. Take your time.
Tracy Beanz says her husband was cured of MsS after 1 year on the carnivore diet
Prayers for you and your wife. I'd download telegram and join some alternative med channels. A lot of MS chatter there.
As someone else said, look into an mms protocol.
Also consider getting vitamin levels checked. Vitamin B12 specifically can cause very real neurological effects when deficient. Pernicious anemia. I had a video bookmarked but it’s no longer on YT all about this and how simple and cheap it is to remedy if you catch it in time via B12 pills or even shots, if you can find an honest doctor willing to do it.
What kind of tests do you mean? Have they done an MRI and confirmed scarring on the brain and spinal cord? Have they done a spinal tap to confirm O-bands in her spinal fluid?
Look into the Wahls Protocol. It's a paleo way of eating developed by a doctor who has PPMS (primary progressive MS). She also has examples of exercises specifically designed to help people with MS maintain their mobility. She went from laying in a reclined wheelchair all day to biking like 20 miles at a time. At one time, she was doing clinical trials on the effects of diet on auto-immune diseases such as MS; I don't know if those are still ongoing. Her book was one of the first I bought when my husband was diagnosed with MS back in 2016. He's never been willing to stick to the strict diet, but I know firsthand how much we are affected by what we eat (I have autoimmune arthritis and it goes into remission when I stop eating processed sugar).
Financially...if you choose to go the pharma route (which I'm normally not a fan of, but MS is scary) the doctor needs to go ahead and get her on an aggressive treatment like Tysabri. The Dr will need to go to bat for her with the insurance company; the insurance company will try to insist that she try something older (and less effective) like copaxone first. My husband's neurologist has done this on several occasions, so if yours won't fight for your wife, find a new one! When the insurance company approves a high priced drug, you will want to enroll in the drug company's financial aid program. It is the only way we were able to afford Tysabri (monthly infusion) for several years and now Keysimpta (administered at home). For both of the medicines, the manufacturer pays the deductible with the first dose of the year.
Prayers for your wife (and you)!
I'm surprised that nobody has mentioned Ivermectin. It's showing great promise in healing myelin sheath injuries and promoting peripheral nerve regeneration.
https://yandex.com/search/?text=ivermectin+myelin