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<div>Looking to raise funds for a proper memorial of “<strong>Collin Teem</strong>” a(n) <strong>American Volunteer </strong>whom lost his life fighting for <strong>Ukraine</strong> in the Russo-Ukrainian War.
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<div><strong>About his life:</strong>
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<div><strong>Collin Teem </strong>was an outstanding young man in his community touching others around him.
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<div>Growing up with the love of fishing and hunting through the years creating friendships that would last a lifetime.
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<div>Collin a high school graduate of White Knoll High School pursued a selfless path of serving his country as a <strong>United States Marine.</strong>
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<div>Obtaining the MOS of a(n) infantry <strong>Machine Gunner. </strong>
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<div>Ending his career in the Marines after 4 years his selflessness did not end. He volunteered to fight for Ukraine in their time of need. It had been stated by a person who will remain unknown that Collin was last seen defending his comrades (Holding the Line) from a(n) enemy advance. Giving the ultimate sacrifice .
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<div>Got Bless his Soul
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<div>Fair Winds and Following Seas…
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Collin Teem : “Hold the Line”

<p>Hi my name is Jacob Lane. Im a military Vet. I have been through alot this year and have had alot of medical issues and countless procedures that have cost me alot of money. I recently have been doing really well I moved into my first house and got an amazing job. A few days ago I expierenced some really bad pain so I went to the hospital to find out that my pancreas was failing. I spent 3 days in the hospital then another 5 in another hospital. Was home for a week then right back in the hospital. Ive been here 3 days now and had a surgery on my chest. During the surgery one of my lungs collapsed. So Im on oxygen until further notice. My job informed me that they cannot pay me for the time off. So any help would be greatly Appreciated. Bills are starting to pile up and its all becoming quite overwhelming. If you cannot afford to donate please keep me in your prayers. 


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Help Jacob Recover

Below is the story from Siyona and her family. kindly bear with us. Our daughter Siyona took step in this world on 12th of September 2019. I still remember that day. We were very happy as i hold her in my arms. She was a healthy baby girl and i still remember her bright and big eyes staring me. We immediately fell in love with her and start thinking of her future. We thought of providing her every needs of her life- a good education and most important a better human. Everyday with her went on so fast when we realized she already turned 4 months. I then began to realize she was not able to hold her head nor turn sideways. She was breastfeeding normally and was gaining her usual weight. Some of our family members told this is normal and she will be be holding her head in few months. We believed and carried on dreaming of her bright future. Days passed on and she was now 5 months. Still she was not holding her head. Now we were worried,so visited our doctor. Our doctor examined and did some neurological exam, few blood tests and a brain scan. Everything was normal and we were told she might be having a benign hypotonia of infancy. Just a bit physiotherapy and nothing much to worry about: I still remember my doctor words. We were happy she was alright and began her physiotherapy. Now she was 6 months, still hypotonic. We knew something was not right and again visited our doctor. Now our doctor advised us to visit a senior neurologist and we did so. I still remember that day, the saddest day of our life, the day when our dreams were shattered. The neurologist after assessing our child and looking the prior reports immediately told us she might be a having a neuromuscular disease only to be confirmed by genetic disease and most probably our child might be having the severe form of the disease. That was the day when we first heard of this disease called SPINAL MUSCULAR ATROPHY. Blood was drawn and sent for genetic testing and we returned with heavy hearts. I was very tensed and started looking after it in internet. I was told about it a bit by my neurologist. It is a progressive neuromuscular disease that gradual weakens the muscles of limbs,swallowing and breathing. You can imagine the outcome. My child can’t sit up nor walk stand, she will not be able to eat and drink and finally not able to breathe on her own. Without timely treatment most of infants with severe form of SMA will be on permanent ventilation within a year of life and rarely survive beyond two years. I was always praying to god that our reports will be negative but i was wrong. Finally got the reports that showed my daughter Siyona had type 1 SMA. My neurologist told me the prognosis and gene therapy was the only cure. Gene therapy drug called Zolgensma costs nearly 2.1 million usd and we are no longer in a position to afford. We need your support to afford my daughter's treatment. I wish to see her stand and run and fulfill her dream. Please donate for my daughter and fulfill her desire to live and achieve her dream. We believe Siyona is one of the luckiest to receive Zolgensma. UPDATE-Utilization of fund.What if?   Lastly what is the plan if target is not met? How will the raised funds be utilised? First of all, seeing the support of all wellwishers all around the globe, I don’t see anything why our target won’t be met. Siyona deserves life and there are so many prayers and efforts that can’t be unheard by the God.  We will achieve the target.  I am her father and I have seen her suffering everyday and if any mishap happens or funds couldn’t be raised, then the funds will be utilized only for alternative available therapy and the supportive care of Siyona. I am a Nepal based doctor and I have seen how difficult is there for a Nepali patient to fight SMA. The remaining funds will be utilised to raise a SMA foundation in Nepal that will work entirely for the upliftment of SMA patients in Nepal including their palliative care. We are already on this process and the legal formalities are delayed by covid. We will soon update the process. Questions: How you are related to your beneficiary? Hello again, I am Anish Kumar Shrestha and Siyona is my niece.Her father Dr Sandeep Shrestha is my father's sister's son.While donations are being done by the generous donors, I have to regularly withdraw the amount. I have attached my bank's account number and other information so that the money will be directly be deposited in my bank account.When the target amount reaches we will directly deposit that amount with Novartis's Avexis with together work of clinic of special children and parents.The drug needs to be purchased first and the remaining balance will be used  for medical treatment costs at the hospital.Incase if the target amount doesn't meet up the parents Nepal bank account will be directly deposited from my US bank account.The fund will be used for available alternative treatment  and palliative care of Siyona plus a SMA foundation will be established that will work entirely for the upliftment of SMA patients in Nepal including their palliative care.  If you require further documents and information we shall provide that .Please contact Dr Sandeep and Aleena for any more required documents. Their facebook profile ids are: Facebook: <a href="https://www.facebook.com/groups/238340680767197/" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/groups/238340680767197/</a> Siyona Shrestha’s father facebook id: <a href="https://www.facebook.com/sandeep.shrestha.520125" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/sandeep.shrestha.520125</a> Siyona Shrestha mother facebook id: <a href="https://www.facebook.com/aleena.gurung.7374" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/aleena.gurung.7374</a> Gofundme organizer facebook id : <a href="https://www.facebook.com/anish.k.shrestha" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.facebook.com/anish.k.shrestha</a> Sincerely Anish Shrestha [email redacted] 323926450 Youtube Siyona video link: <a href="https://www.youtube.com/watch?v=CdMTsb0CKyQ" target="_blank" class="" rel="nofollow noopener noreferrer">https://www.youtube.com/watch?v=CdMTsb0CKyQ</a>

Save Siyona fight Spinal muscular atrophy