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Interview 502 with Mike & Angie Kendig
Mike & Angie Kendig's son Ethan is 19 years old
He has developed some very life-altering side effects from what doctors believe to be a mix of long-term co vid /vac cination side effects.
Ethan's symptoms have not improved they are getting worse. Some of those symptoms are fatigue, brain fog, dizziness, insomnia, constant headaches/migraines, constant body aches, stomach aches, depression, anxiety, phantom smells, and unable to walk without assistance. He uses a walker in the house and they use a wheelchair when they are traveling outside the home. Ethan has also been suffering from repeated non-epileptic seizures and they are NOT getting any better! They are MORE INTENSE. As they are lasting longer and are stronger & he is unable to feel his arms and legs at times. These seizures have lasted up to 3 hours long during one episode.
The seizures can happen anytime but can also be 'triggered' by loud noises such as motorcycles, sirens, doorbells and phones ringing. As you can imagine, that would be very upsetting for the entire family after hearing something loud go by on the main street out front of their home KNOWING IT WILL CAUSE A TRIGGER FOR ANOTHER SEIZURE THAT YOU CANNOT PREVENT! AND ... NEITHER CAN THE DOCTORS... which is why we are raising money to help this family collect the things they can and alter their home in any way they are able that can prevent some of what Ethan is experiencing... until they can get the answers they need.
Ethan wants to get back to the goals and dreams of his life but those are currently on hold since this all started altering his life during his senior year of high school...
*Mike and Angie have taken Ethan to some of the Top Specialists @ the Cleveland Clinic, & Ohio State. The Mayo Clinic would not even see Ethan after filling out all of the required paperwork. They have had Doctors and Specialists be gracious enough to come to their home and try to wrap their minds around Ethan's condition. Ethan has an UPCOMING APT w Northern University in June. They are currently speaking with another family whose son is suffering the same way Ethan is, and as heartbreaking as it is, I am thankful they have someone who understands what they are going thru. It has to be a very difficult place to be. We will continue to pray for answers AND solutions.
They have tried: the use of an infrared lamp and infrared sauna, noise-canceling headphones, a hyperbaric oxygen chamber, continued appointments with specialists and several tests...they are currently staying at a home offered to them in the country to try a more peaceful scenery and atmosphere (temporarily) while having a company come to their home and add foam insulation to help with the noise during the time while trying to discover what the cause/solution will be. They have recently started him on a special diet- (gluten, dairy, sugar & corn free/food coloring) as allergy tests are showing he is allergic to these ingredients.
With so many tests and not enough answers right now we are asking for monetary donations to help their family with medical bills, and extra monthly expenses as well as donations to help with the things I mentioned above.
**Other items they will need help with would be: insulated windows/inserts to help soundproof his room (until they can find solutions) Meds not covered by insurance, A Grounding Mat, Doctors that do not take medical insurance (natural approaches), Supplements and Special Diet needs, as well as many other things along the way that are unknown at this time.
**If you know of anyone who could donate supplies or knowledge to this family please get ahold of one of us.**
WE NEED GOD TO SHOW UP BIG HERE!!
I have started a FB group page for Ethan "We love you Ethan" .
Feel free to join! That is where we will let you know 'other ways you can help, love, support and encourage' each one of them bc being a caretaker is JUST AS HARD as the struggle of your loved one.
Thank you for your prayers, your love, & your generosity
Go Fund Me Link:
https://www.gofundme.com/.../plz-show-the-kendig-family...
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